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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 23:16:18 UTC

Update Date

2022-03-07 02:55:35 UTC

HMDB ID

HMDB0037996

Secondary Accession Numbers

HMDB37996

Metabolite Identification

Common Name

Cyanidin 3-laminaribioside

Description

Cyanidin 3-laminaribioside belongs to the class of organic compounds known as anthocyanidin-3-o-glycosides. These are phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C3-position. Thus, cyanidin 3-laminaribioside is considered to be a flavonoid. Cyanidin 3-laminaribioside has been detected, but not quantified in, several different foods, such as garden onion (var.), onion-family vegetables, red onion, green onion, and garden onions (Allium cepa). This could make cyanidin 3-laminaribioside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Cyanidin 3-laminaribioside.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 02241207482D          

 43 47  0  0  0  0            999 V2000
   -5.5693    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2837   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2837   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5693   -1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8548   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8548   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1403    0.2225    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
   -4.1403   -1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4259   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4259   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969    1.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114    1.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825    1.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5680    1.4600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9981    0.2225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969    2.2850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5693   -2.2526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401   -1.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6004   -1.9825    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6556   -2.8056    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3960   -3.1694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0813   -2.7100    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0261   -1.8869    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2857   -1.5231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114   -1.4275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8218   -3.0738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4512   -3.9925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1917   -4.3563    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2469   -5.1795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9874   -5.5433    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6726   -5.0839    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6174   -4.2607    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8770   -3.8970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3027   -3.8014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0432   -4.1651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4131   -5.4477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0425   -6.3664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5616   -5.6389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0297   -3.2650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1953   -0.7955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  2  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  7 10  2  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 13 11  2  0  0  0  0
 11 14  1  0  0  0  0
 12 13  1  0  0  0  0
 12 16  2  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 20  1  0  0  0  0
 16 17  1  0  0  0  0
  2 18  1  0  0  0  0
  9 28  1  0  0  0  0
 12 19  1  0  0  0  0
 22 21  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
 26 28  1  6  0  0  0
 25 29  1  1  0  0  0
 24 30  1  6  0  0  0
 31 30  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 36  1  0  0  0  0
 35 37  1  1  0  0  0
 37 38  1  0  0  0  0
 34 39  1  6  0  0  0
 33 40  1  1  0  0  0
 32 41  1  6  0  0  0
 23 42  1  1  0  0  0
 21 43  1  0  0  0  0
M  CHG  1   7   1
M  END

HMDB0037996
     RDKit          3D
Cyanidin 3-laminaribioside
 74 78  0  0  0  0  0  0  0  0999 V2000
    4.7915   -1.2796   -2.0738 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0770   -1.7152   -0.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7594   -0.6384    0.0331 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0114    0.5085    0.1731 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7670    0.3056    0.7797 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9264   -0.1384   -0.1930 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9022    0.7230   -0.5658 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6119   -0.0342   -0.3488 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4262   -0.4772    0.9357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6068    0.7189   -0.8772 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7093    0.1367   -0.5072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8055   -0.4283   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9066   -1.8396   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9956   -2.5756   -0.0143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0711   -3.9500   -0.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0488   -4.6284   -0.8306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2129   -4.6666    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2546   -3.9973    0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3857   -4.7317    1.0950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1652   -2.6399    0.9466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0542   -1.9036    0.5885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9644   -0.6319    0.7899 O   0  0  0  0  0  3  0  0  0  0  0  0
   -3.9164    0.1278    0.4641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0417    1.5239    0.7876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9580    1.8961    1.7816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1939    3.1933    2.1194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4976    4.1781    1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7575    5.5081    1.8165 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5922    3.8525    0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9222    4.8852   -0.1685 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3664    2.5046    0.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4109    0.6795   -2.2998 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6387    1.5686   -2.5172 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7150    1.8637   -3.9935 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9407    0.6792   -4.6597 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9621    1.0072   -2.0761 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9353    1.9636   -2.3569 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8624   -0.5150    2.0200 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2362    0.1022    3.1303 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3431   -0.5534    2.4240 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5081   -1.2029    3.6525 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2106   -1.1726    1.3760 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5325   -0.8017    1.6107 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9951   -1.7374   -2.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8336   -2.5448   -0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571   -2.1086   -0.3411 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6741   -0.3546   -0.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4313    1.3389    1.0923 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9085    1.6674    0.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6938   -0.9558   -0.9975 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9495    0.0011    1.6234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4273    1.7908   -0.5703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0664   -2.3214   -0.8293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2002   -4.2189   -1.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2333   -5.7263   -0.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1626   -4.8522    0.4353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9948   -2.1239    1.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5048    1.1293    2.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9087    3.4226    2.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2373    6.2292    1.3146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2557    4.6622   -0.8911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6817    2.3257   -0.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4543    2.5048   -1.9538 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4840    2.6412   -4.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2696    2.2718   -4.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3909    0.6495   -5.4884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2403    0.0762   -2.5785 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2300    2.4404   -1.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4266   -1.5166    1.9405 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5910    1.0241    3.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6488    0.5117    2.5265 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3666   -0.9213    4.0557 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1733   -2.2830    1.3754 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9733   -0.4268    0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  2  0
 10 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 33 36  1  0
 36 37  1  0
  5 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 42  3  1  0
 36  7  1  0
 23 12  1  0
 31 24  1  0
 21 14  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  3 47  1  6
  5 48  1  1
  7 49  1  1
  8 50  1  6
  9 51  1  0
 10 52  1  1
 13 53  1  0
 16 54  1  0
 17 55  1  0
 19 56  1  0
 20 57  1  0
 25 58  1  0
 26 59  1  0
 28 60  1  0
 30 61  1  0
 31 62  1  0
 33 63  1  1
 34 64  1  0
 34 65  1  0
 35 66  1  0
 36 67  1  6
 37 68  1  0
 38 69  1  6
 39 70  1  0
 40 71  1  1
 41 72  1  0
 42 73  1  6
 43 74  1  0
M  CHG  1  22   1
M  END


  Mrv0541 02241207482D          

 43 47  0  0  0  0            999 V2000
   -5.5693    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2837   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2837   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5693   -1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8548   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8548   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1403    0.2225    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
   -4.1403   -1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4259   -1.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4259   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969    1.4600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114    1.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825    0.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825    1.0475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5680    1.4600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9981    0.2225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9969    2.2850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5693   -2.2526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401   -1.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6004   -1.9825    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6556   -2.8056    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3960   -3.1694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0813   -2.7100    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0261   -1.8869    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2857   -1.5231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7114   -1.4275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8218   -3.0738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4512   -3.9925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1917   -4.3563    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2469   -5.1795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9874   -5.5433    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6726   -5.0839    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6174   -4.2607    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8770   -3.8970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3027   -3.8014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0432   -4.1651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4131   -5.4477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0425   -6.3664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5616   -5.6389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0297   -3.2650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1953   -0.7955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  2  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  7  6  1  0  0  0  0
  6  5  1  0  0  0  0
  5  8  1  0  0  0  0
  7 10  2  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 13 11  2  0  0  0  0
 11 14  1  0  0  0  0
 12 13  1  0  0  0  0
 12 16  2  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  4 20  1  0  0  0  0
 16 17  1  0  0  0  0
  2 18  1  0  0  0  0
  9 28  1  0  0  0  0
 12 19  1  0  0  0  0
 22 21  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
 26 28  1  6  0  0  0
 25 29  1  1  0  0  0
 24 30  1  6  0  0  0
 31 30  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 36  1  0  0  0  0
 35 37  1  1  0  0  0
 37 38  1  0  0  0  0
 34 39  1  6  0  0  0
 33 40  1  1  0  0  0
 32 41  1  6  0  0  0
 23 42  1  1  0  0  0
 21 43  1  0  0  0  0
M  CHG  1   7   1
M  END
> <DATABASE_ID>
HMDB0037996

> <DATABASE_NAME>
hmdb

> <SMILES>
OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](CO)O[C@@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC(O)=C(O)C=C3)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H30O16/c28-7-17-19(34)21(36)22(37)26(41-17)43-25-20(35)18(8-29)42-27(23(25)38)40-16-6-11-13(32)4-10(30)5-15(11)39-24(16)9-1-2-12(31)14(33)3-9/h1-6,17-23,25-29,34-38H,7-8H2,(H3-,30,31,32,33)/p+1/t17-,18-,19-,20-,21+,22-,23-,25+,26+,27-/m1/s1

> <INCHI_KEY>
YXBNLEZVGITYGW-SQLAXTICSA-O

> <FORMULA>
C27H31O16

> <MOLECULAR_WEIGHT>
611.5254

> <EXACT_MASS>
611.161209944

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
57.92105222793033

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-{[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-1λ⁴-chromen-1-ylium

> <ALOGPS_LOGP>
0.06

> <JCHEM_LOGP>
-1.7297000000000002

> <ALOGPS_LOGS>
-2.55

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.45795600870925

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.38832910835931

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6552632927077093

> <JCHEM_POLAR_SURFACE_AREA>
272.59

> <JCHEM_REFRACTIVITY>
148.67080000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.84e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-1λ⁴-chromen-1-ylium

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037996
     RDKit          3D
Cyanidin 3-laminaribioside
 74 78  0  0  0  0  0  0  0  0999 V2000
    4.7915   -1.2796   -2.0738 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0770   -1.7152   -0.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7594   -0.6384    0.0331 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0114    0.5085    0.1731 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7670    0.3056    0.7797 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9264   -0.1384   -0.1930 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9022    0.7230   -0.5658 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6119   -0.0342   -0.3488 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4262   -0.4772    0.9357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6068    0.7189   -0.8772 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7093    0.1367   -0.5072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8055   -0.4283   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9066   -1.8396   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9956   -2.5756   -0.0143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0711   -3.9500   -0.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0488   -4.6284   -0.8306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2129   -4.6666    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2546   -3.9973    0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3857   -4.7317    1.0950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1652   -2.6399    0.9466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0542   -1.9036    0.5885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9644   -0.6319    0.7899 O   0  0  0  0  0  3  0  0  0  0  0  0
   -3.9164    0.1278    0.4641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0417    1.5239    0.7876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9580    1.8961    1.7816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1939    3.1933    2.1194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4976    4.1781    1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7575    5.5081    1.8165 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5922    3.8525    0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9222    4.8852   -0.1685 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3664    2.5046    0.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4109    0.6795   -2.2998 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6387    1.5686   -2.5172 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7150    1.8637   -3.9935 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9407    0.6792   -4.6597 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9621    1.0072   -2.0761 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9353    1.9636   -2.3569 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8624   -0.5150    2.0200 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2362    0.1022    3.1303 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3431   -0.5534    2.4240 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5081   -1.2029    3.6525 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2106   -1.1726    1.3760 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5325   -0.8017    1.6107 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9951   -1.7374   -2.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8336   -2.5448   -0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571   -2.1086   -0.3411 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6741   -0.3546   -0.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4313    1.3389    1.0923 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9085    1.6674    0.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6938   -0.9558   -0.9975 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9495    0.0011    1.6234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4273    1.7908   -0.5703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0664   -2.3214   -0.8293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2002   -4.2189   -1.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2333   -5.7263   -0.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1626   -4.8522    0.4353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9948   -2.1239    1.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5048    1.1293    2.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9087    3.4226    2.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2373    6.2292    1.3146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2557    4.6622   -0.8911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6817    2.3257   -0.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4543    2.5048   -1.9538 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4840    2.6412   -4.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2696    2.2718   -4.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3909    0.6495   -5.4884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2403    0.0762   -2.5785 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2300    2.4404   -1.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4266   -1.5166    1.9405 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5910    1.0241    3.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6488    0.5117    2.5265 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3666   -0.9213    4.0557 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1733   -2.2830    1.3754 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9733   -0.4268    0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  2  0
 10 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 33 36  1  0
 36 37  1  0
  5 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 42  3  1  0
 36  7  1  0
 23 12  1  0
 31 24  1  0
 21 14  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  3 47  1  6
  5 48  1  1
  7 49  1  1
  8 50  1  6
  9 51  1  0
 10 52  1  1
 13 53  1  0
 16 54  1  0
 17 55  1  0
 19 56  1  0
 20 57  1  0
 25 58  1  0
 26 59  1  0
 28 60  1  0
 30 61  1  0
 31 62  1  0
 33 63  1  1
 34 64  1  0
 34 65  1  0
 35 66  1  0
 36 67  1  6
 37 68  1  0
 38 69  1  6
 39 70  1  0
 40 71  1  1
 41 72  1  0
 42 73  1  6
 43 74  1  0
M  CHG  1  22   1
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0     -10.396   0.415   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -11.730  -0.355   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -11.730  -1.895   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.396  -2.665   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.062  -1.895   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.062  -0.355   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -7.729   0.415   0.000  0.00  0.00           O+1
HETATM    8  C   UNK     0      -7.729  -2.665   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.395  -1.895   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.395  -0.355   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.061   0.415   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.728   2.725   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.061   1.955   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.728  -0.355   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.394   0.415   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.394   1.955   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.060   2.725   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0     -13.063   0.415   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -3.728   4.265   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0     -10.396  -4.205   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.262  -3.022   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.121  -3.701   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.224  -5.237   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.606  -5.916   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.885  -5.059   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.782  -3.522   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.400  -2.843   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -5.061  -2.665   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -5.267  -5.738   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -2.709  -7.453   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -4.091  -8.132   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.194  -9.668   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -5.576 -10.347   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -6.856  -9.490   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -6.752  -7.953   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -5.370  -7.274   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -8.032  -7.096   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -9.414  -7.775   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -8.238 -10.169   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -5.679 -11.884   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      -2.915 -10.526   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       0.055  -6.095   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       0.365  -1.485   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   18                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
CONECT    5    4    6    8                                                  
CONECT    6    1    7    5                                                  
CONECT    7    6   10                                                       
CONECT    8    5    9                                                       
CONECT    9    8   10   28                                                  
CONECT   10    7    9   11                                                  
CONECT   11   10   13   14                                                  
CONECT   12   13   16   19                                                  
CONECT   13   11   12                                                       
CONECT   14   11   15                                                       
CONECT   15   14   16                                                       
CONECT   16   12   15   17                                                  
CONECT   17   16                                                            
CONECT   18    2                                                            
CONECT   19   12                                                            
CONECT   20    4                                                            
CONECT   21   22   43                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24   42                                                  
CONECT   24   23   25   30                                                  
CONECT   25   24   26   29                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26   22                                                       
CONECT   28    9   26                                                       
CONECT   29   25                                                            
CONECT   30   24   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33   41                                                  
CONECT   33   32   34   40                                                  
CONECT   34   33   35   39                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35   31                                                       
CONECT   37   35   38                                                       
CONECT   38   37                                                            
CONECT   39   34                                                            
CONECT   40   33                                                            
CONECT   41   32                                                            
CONECT   42   23                                                            
CONECT   43   21                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

COMPND    HMDB0037996
HETATM    1  O1  UNL     1       4.792  -1.280  -2.074  1.00  0.00           O  
HETATM    2  C1  UNL     1       5.077  -1.715  -0.783  1.00  0.00           C  
HETATM    3  C2  UNL     1       5.759  -0.638   0.033  1.00  0.00           C  
HETATM    4  O2  UNL     1       5.011   0.508   0.173  1.00  0.00           O  
HETATM    5  C3  UNL     1       3.767   0.306   0.780  1.00  0.00           C  
HETATM    6  O3  UNL     1       2.926  -0.138  -0.193  1.00  0.00           O  
HETATM    7  C4  UNL     1       1.902   0.723  -0.566  1.00  0.00           C  
HETATM    8  C5  UNL     1       0.612  -0.034  -0.349  1.00  0.00           C  
HETATM    9  O4  UNL     1       0.426  -0.477   0.936  1.00  0.00           O  
HETATM   10  C6  UNL     1      -0.607   0.719  -0.877  1.00  0.00           C  
HETATM   11  O5  UNL     1      -1.709   0.137  -0.507  1.00  0.00           O  
HETATM   12  C7  UNL     1      -2.805  -0.428  -0.136  1.00  0.00           C  
HETATM   13  C8  UNL     1      -2.907  -1.840  -0.361  1.00  0.00           C  
HETATM   14  C9  UNL     1      -3.996  -2.576  -0.014  1.00  0.00           C  
HETATM   15  C10 UNL     1      -4.071  -3.950  -0.243  1.00  0.00           C  
HETATM   16  O6  UNL     1      -3.049  -4.628  -0.831  1.00  0.00           O  
HETATM   17  C11 UNL     1      -5.213  -4.667   0.133  1.00  0.00           C  
HETATM   18  C12 UNL     1      -6.255  -3.997   0.728  1.00  0.00           C  
HETATM   19  O7  UNL     1      -7.386  -4.732   1.095  1.00  0.00           O  
HETATM   20  C13 UNL     1      -6.165  -2.640   0.947  1.00  0.00           C  
HETATM   21  C14 UNL     1      -5.054  -1.904   0.589  1.00  0.00           C  
HETATM   22  O8  UNL     1      -4.964  -0.632   0.790  1.00  0.00           O1+
HETATM   23  C15 UNL     1      -3.916   0.128   0.464  1.00  0.00           C  
HETATM   24  C16 UNL     1      -4.042   1.524   0.788  1.00  0.00           C  
HETATM   25  C17 UNL     1      -4.958   1.896   1.782  1.00  0.00           C  
HETATM   26  C18 UNL     1      -5.194   3.193   2.119  1.00  0.00           C  
HETATM   27  C19 UNL     1      -4.498   4.178   1.450  1.00  0.00           C  
HETATM   28  O9  UNL     1      -4.758   5.508   1.817  1.00  0.00           O  
HETATM   29  C20 UNL     1      -3.592   3.853   0.469  1.00  0.00           C  
HETATM   30  O10 UNL     1      -2.922   4.885  -0.168  1.00  0.00           O  
HETATM   31  C21 UNL     1      -3.366   2.505   0.138  1.00  0.00           C  
HETATM   32  O11 UNL     1      -0.411   0.679  -2.300  1.00  0.00           O  
HETATM   33  C22 UNL     1       0.639   1.569  -2.517  1.00  0.00           C  
HETATM   34  C23 UNL     1       0.715   1.864  -3.993  1.00  0.00           C  
HETATM   35  O12 UNL     1       0.941   0.679  -4.660  1.00  0.00           O  
HETATM   36  C24 UNL     1       1.962   1.007  -2.076  1.00  0.00           C  
HETATM   37  O13 UNL     1       2.935   1.964  -2.357  1.00  0.00           O  
HETATM   38  C25 UNL     1       3.862  -0.515   2.020  1.00  0.00           C  
HETATM   39  O14 UNL     1       3.236   0.102   3.130  1.00  0.00           O  
HETATM   40  C26 UNL     1       5.343  -0.553   2.424  1.00  0.00           C  
HETATM   41  O15 UNL     1       5.508  -1.203   3.652  1.00  0.00           O  
HETATM   42  C27 UNL     1       6.211  -1.173   1.376  1.00  0.00           C  
HETATM   43  O16 UNL     1       7.532  -0.802   1.611  1.00  0.00           O  
HETATM   44  H1  UNL     1       3.995  -1.737  -2.467  1.00  0.00           H  
HETATM   45  H2  UNL     1       5.834  -2.545  -0.913  1.00  0.00           H  
HETATM   46  H3  UNL     1       4.157  -2.109  -0.341  1.00  0.00           H  
HETATM   47  H4  UNL     1       6.674  -0.355  -0.528  1.00  0.00           H  
HETATM   48  H5  UNL     1       3.431   1.339   1.092  1.00  0.00           H  
HETATM   49  H6  UNL     1       1.909   1.667   0.002  1.00  0.00           H  
HETATM   50  H7  UNL     1       0.694  -0.956  -0.997  1.00  0.00           H  
HETATM   51  H8  UNL     1       0.949   0.001   1.623  1.00  0.00           H  
HETATM   52  H9  UNL     1      -0.427   1.791  -0.570  1.00  0.00           H  
HETATM   53  H10 UNL     1      -2.066  -2.321  -0.829  1.00  0.00           H  
HETATM   54  H11 UNL     1      -2.200  -4.219  -1.134  1.00  0.00           H  
HETATM   55  H12 UNL     1      -5.233  -5.726  -0.061  1.00  0.00           H  
HETATM   56  H13 UNL     1      -8.163  -4.852   0.435  1.00  0.00           H  
HETATM   57  H14 UNL     1      -6.995  -2.124   1.418  1.00  0.00           H  
HETATM   58  H15 UNL     1      -5.505   1.129   2.308  1.00  0.00           H  
HETATM   59  H16 UNL     1      -5.909   3.423   2.891  1.00  0.00           H  
HETATM   60  H17 UNL     1      -4.237   6.229   1.315  1.00  0.00           H  
HETATM   61  H18 UNL     1      -2.256   4.662  -0.891  1.00  0.00           H  
HETATM   62  H19 UNL     1      -2.682   2.326  -0.660  1.00  0.00           H  
HETATM   63  H20 UNL     1       0.454   2.505  -1.954  1.00  0.00           H  
HETATM   64  H21 UNL     1       1.484   2.641  -4.192  1.00  0.00           H  
HETATM   65  H22 UNL     1      -0.270   2.272  -4.319  1.00  0.00           H  
HETATM   66  H23 UNL     1       0.391   0.650  -5.488  1.00  0.00           H  
HETATM   67  H24 UNL     1       2.240   0.076  -2.579  1.00  0.00           H  
HETATM   68  H25 UNL     1       3.230   2.440  -1.541  1.00  0.00           H  
HETATM   69  H26 UNL     1       3.427  -1.517   1.940  1.00  0.00           H  
HETATM   70  H27 UNL     1       3.591   1.024   3.242  1.00  0.00           H  
HETATM   71  H28 UNL     1       5.649   0.512   2.527  1.00  0.00           H  
HETATM   72  H29 UNL     1       6.367  -0.921   4.056  1.00  0.00           H  
HETATM   73  H30 UNL     1       6.173  -2.283   1.375  1.00  0.00           H  
HETATM   74  H31 UNL     1       7.973  -0.427   0.803  1.00  0.00           H  
CONECT    1    2   44
CONECT    2    3   45   46
CONECT    3    4   42   47
CONECT    4    5
CONECT    5    6   38   48
CONECT    6    7
CONECT    7    8   36   49
CONECT    8    9   10   50
CONECT    9   51
CONECT   10   11   32   52
CONECT   11   12
CONECT   12   13   13   23
CONECT   13   14   53
CONECT   14   15   15   21
CONECT   15   16   17
CONECT   16   54
CONECT   17   18   18   55
CONECT   18   19   20
CONECT   19   56
CONECT   20   21   21   57
CONECT   21   22
CONECT   22   23   23
CONECT   23   24
CONECT   24   25   25   31
CONECT   25   26   58
CONECT   26   27   27   59
CONECT   27   28   29
CONECT   28   60
CONECT   29   30   31   31
CONECT   30   61
CONECT   31   62
CONECT   32   33
CONECT   33   34   36   63
CONECT   34   35   64   65
CONECT   35   66
CONECT   36   37   67
CONECT   37   68
CONECT   38   39   40   69
CONECT   39   70
CONECT   40   41   42   71
CONECT   41   72
CONECT   42   43   73
CONECT   43   74
END

HMDB0037996
     RDKit          3D
Cyanidin 3-laminaribioside
 74 78  0  0  0  0  0  0  0  0999 V2000
    4.7915   -1.2796   -2.0738 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0770   -1.7152   -0.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7594   -0.6384    0.0331 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0114    0.5085    0.1731 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7670    0.3056    0.7797 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9264   -0.1384   -0.1930 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9022    0.7230   -0.5658 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6119   -0.0342   -0.3488 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4262   -0.4772    0.9357 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6068    0.7189   -0.8772 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7093    0.1367   -0.5072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8055   -0.4283   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9066   -1.8396   -0.3611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9956   -2.5756   -0.0143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0711   -3.9500   -0.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0488   -4.6284   -0.8306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2129   -4.6666    0.1326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2546   -3.9973    0.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3857   -4.7317    1.0950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1652   -2.6399    0.9466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0542   -1.9036    0.5885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9644   -0.6319    0.7899 O   0  0  0  0  0  3  0  0  0  0  0  0
   -3.9164    0.1278    0.4641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0417    1.5239    0.7876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9580    1.8961    1.7816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1939    3.1933    2.1194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4976    4.1781    1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7575    5.5081    1.8165 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5922    3.8525    0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9222    4.8852   -0.1685 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3664    2.5046    0.1376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4109    0.6795   -2.2998 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6387    1.5686   -2.5172 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7150    1.8637   -3.9935 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9407    0.6792   -4.6597 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9621    1.0072   -2.0761 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9353    1.9636   -2.3569 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8624   -0.5150    2.0200 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2362    0.1022    3.1303 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3431   -0.5534    2.4240 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5081   -1.2029    3.6525 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2106   -1.1726    1.3760 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5325   -0.8017    1.6107 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9951   -1.7374   -2.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8336   -2.5448   -0.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571   -2.1086   -0.3411 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6741   -0.3546   -0.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4313    1.3389    1.0923 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9085    1.6674    0.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6938   -0.9558   -0.9975 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9495    0.0011    1.6234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4273    1.7908   -0.5703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0664   -2.3214   -0.8293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2002   -4.2189   -1.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2333   -5.7263   -0.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1626   -4.8522    0.4353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9948   -2.1239    1.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5048    1.1293    2.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9087    3.4226    2.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2373    6.2292    1.3146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2557    4.6622   -0.8911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6817    2.3257   -0.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4543    2.5048   -1.9538 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4840    2.6412   -4.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2696    2.2718   -4.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3909    0.6495   -5.4884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2403    0.0762   -2.5785 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2300    2.4404   -1.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4266   -1.5166    1.9405 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5910    1.0241    3.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6488    0.5117    2.5265 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3666   -0.9213    4.0557 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1733   -2.2830    1.3754 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9733   -0.4268    0.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  2  0
 10 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 33 36  1  0
 36 37  1  0
  5 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 42  3  1  0
 36  7  1  0
 23 12  1  0
 31 24  1  0
 21 14  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  3 47  1  6
  5 48  1  1
  7 49  1  1
  8 50  1  6
  9 51  1  0
 10 52  1  1
 13 53  1  0
 16 54  1  0
 17 55  1  0
 19 56  1  0
 20 57  1  0
 25 58  1  0
 26 59  1  0
 28 60  1  0
 30 61  1  0
 31 62  1  0
 33 63  1  1
 34 64  1  0
 34 65  1  0
 35 66  1  0
 36 67  1  6
 37 68  1  0
 38 69  1  6
 39 70  1  0
 40 71  1  1
 41 72  1  0
 42 73  1  6
 43 74  1  0
M  CHG  1  22   1
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Cyanidin 3-O-beta-(3''-O-beta-D-glucosyl-glucoside)	HMDB

Chemical Formula

C₂₇H₃₁O₁₆

Average Molecular Weight

611.5254

Monoisotopic Molecular Weight

611.161209944

IUPAC Name

3-{[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-1λ⁴-chromen-1-ylium

Traditional Name

3-{[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-1λ⁴-chromen-1-ylium

CAS Registry Number

53696-63-2

SMILES

OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](CO)O[C@@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC(O)=C(O)C=C3)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C27H30O16/c28-7-17-19(34)21(36)22(37)26(41-17)43-25-20(35)18(8-29)42-27(23(25)38)40-16-6-11-13(32)4-10(30)5-15(11)39-24(16)9-1-2-12(31)14(33)3-9/h1-6,17-23,25-29,34-38H,7-8H2,(H3-,30,31,32,33)/p+1/t17-,18-,19-,20-,21+,22-,23-,25+,26+,27-/m1/s1

InChI Key

YXBNLEZVGITYGW-SQLAXTICSA-O

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthocyanidin-3-o-glycosides. These are phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C3-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Anthocyanidin-3-O-glycosides

Alternative Parents

Substituents

Anthocyanidin-3-o-glycoside
Flavonoid-3-o-glycoside
Hydroxyflavonoid
3'-hydroxyflavonoid
4'-hydroxyflavonoid
7-hydroxyflavonoid
5-hydroxyflavonoid
Anthocyanidin
O-glycosyl compound
Glycosyl compound
Disaccharide
Benzopyran
1-benzopyran
Catechol
1-hydroxy-4-unsubstituted benzenoid
Phenol
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Benzenoid
Oxane
Heteroaromatic compound
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Polyol
Acetal
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organooxygen compound
Organic cation
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0037996)
Cytoplasm (HMDB: HMDB0037996)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037996)

Source

Exogenous

Exogenous (HMDB: HMDB0037996)

Food

Food (HMDB: HMDB0037996)

Herb and spice

Herb

Welsh onion (FooDB: FOOD00241)

Vegetable

Onion-family vegetable

Garden onion (FooDB: FOOD00006)
Garden onion (var.) (FooDB: FOOD00226)
Onion-family vegetables (FooDB: FOOD00855)
Green onion (FooDB: FOOD00963)
Red onion (FooDB: FOOD00962)

Endogenous

Plant

Plant (HMDB: HMDB0037996)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0037996)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.84 g/L	ALOGPS
logP	0.06	ALOGPS
logP	-1.7	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	6.39	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	272.59 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	148.67 m³·mol⁻¹	ChemAxon
Polarizability	57.92 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	235.666	30932474
DeepCCS	[M-H]-	233.645	30932474
DeepCCS	[M-2H]-	267.386	30932474
DeepCCS	[M+Na]+	241.665	30932474
AllCCS	[M+H]+	232.0	32859911
AllCCS	[M+H-H2O]+	230.8	32859911
AllCCS	[M+NH4]+	233.1	32859911
AllCCS	[M+Na]+	233.4	32859911
AllCCS	[M-H]-	227.0	32859911
AllCCS	[M+Na-2H]-	229.1	32859911
AllCCS	[M+HCOO]-	231.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Cyanidin 3-laminaribioside	OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](CO)O[C@@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC(O)=C(O)C=C3)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	6111.6	Standard polar	33892256
Cyanidin 3-laminaribioside	OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](CO)O[C@@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC(O)=C(O)C=C3)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5455.9	Standard non polar	33892256
Cyanidin 3-laminaribioside	OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](CO)O[C@@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC(O)=C(O)C=C3)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5661.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Cyanidin 3-laminaribioside,1TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5363.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #10	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@H]1O	5375.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #11	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@H]1O	5360.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	5363.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5377.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #4	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C=C12	5412.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #5	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5423.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #6	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	5391.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #7	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5393.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #8	C[Si](C)(C)O[C@H]1[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	5393.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TMS,isomer #9	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5373.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5235.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5240.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	5242.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #12	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C=C12	5229.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #13	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5235.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #14	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5192.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #15	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	5191.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #16	C[Si](C)(C)O[C@H]1[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	5229.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #17	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	5216.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #18	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@H]1O	5226.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #19	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	5229.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5225.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5235.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5239.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #22	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5201.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5196.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5249.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	5227.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #26	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	5239.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	5234.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #28	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5233.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #29	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5183.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5233.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #30	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	5189.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #31	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C=C12	5222.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #32	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C=C12	5226.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #33	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C=C12	5231.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #34	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C=C12	5247.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #35	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5226.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #36	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5230.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #37	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5234.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #38	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5250.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #39	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	5182.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5192.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #40	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	5194.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #41	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	5180.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #42	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)=CC=C1O	5178.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #43	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	5190.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #44	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	5206.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #45	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	5226.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #46	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5181.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #47	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O	5181.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #48	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	5194.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #49	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	5208.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5188.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #50	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@H]1O	5232.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #51	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@H]1O	5243.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #52	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5246.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #53	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@@H]1CO	5221.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #54	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@H]1O	5235.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #55	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C	5233.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5234.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	5220.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5236.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	5235.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5073.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5063.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #100	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5034.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #101	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	5011.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #102	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4997.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #103	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	5016.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #104	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	5083.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #105	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	5086.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #106	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	5094.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #107	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	5068.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #108	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	5065.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #109	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	5066.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5008.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #110	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5063.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #111	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5044.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #112	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5066.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #113	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5085.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #114	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	5032.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #115	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	5038.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #116	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	4994.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #117	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O	4980.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #118	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	4997.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #119	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	5016.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5000.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #120	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	5079.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #121	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	4989.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #122	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)=CC=C1O	4975.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #123	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	4990.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #124	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	5008.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #125	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C=C12	5057.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #126	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C=C12	5050.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #127	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C=C12	5069.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #128	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O)C=C12	5055.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #129	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O[Si](C)(C)C)C=C12	5064.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5085.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #130	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=C12	5077.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #131	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5075.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #132	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5066.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #133	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5091.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #134	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	5005.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #135	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	5003.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #136	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5072.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #137	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5079.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #138	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4993.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #139	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4990.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	5060.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #140	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5095.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #141	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	5010.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #142	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	5005.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #143	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	5028.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #144	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	5025.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #145	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	5089.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #146	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)=CC=C1O	4994.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #147	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	4992.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #148	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	5014.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #149	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	5062.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5073.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #150	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	4998.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #151	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	5000.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #152	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	5053.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #153	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC=C1O	5022.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #154	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O[Si](C)(C)C	5068.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #155	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5081.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #156	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O	5003.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #157	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	5003.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #158	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	5023.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #159	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	5007.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	5051.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #160	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	5010.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #161	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C1O	5031.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #162	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@@H]1CO	5070.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #163	C[Si](C)(C)O[C@H]1[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5074.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #164	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@H]1O	5078.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #165	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@H]1O[Si](C)(C)C	5062.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5078.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5019.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5012.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5090.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5093.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	5077.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #22	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5086.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	5066.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5093.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5070.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #26	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5051.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	5022.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #28	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5028.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #29	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	5001.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5035.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #30	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5032.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #31	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5043.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #32	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	5014.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #33	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5019.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #34	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4992.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #35	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5024.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #36	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	5097.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #37	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5102.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #38	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	5088.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #39	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5107.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5027.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #40	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5074.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #41	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	5062.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #42	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5078.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #43	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	5066.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #44	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	5098.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #45	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	5081.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #46	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	5082.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #47	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	5099.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #48	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	5045.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #49	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	5037.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5101.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #50	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	5090.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #51	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	5078.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #52	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	5081.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #53	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	5088.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #54	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5072.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #55	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5001.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #56	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	4994.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #57	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C=C12	5057.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #58	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C=C12	5051.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #59	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C=C12	5065.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	5059.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #60	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C=C12	5068.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #61	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5081.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #62	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5068.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #63	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5085.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #64	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5091.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #65	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	5014.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #66	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	5013.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #67	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5010.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #68	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O	4996.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #69	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	5020.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	5089.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #70	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	5028.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #71	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	5067.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #72	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	5001.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #73	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)=CC=C1O	4987.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #74	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	5011.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #75	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	5021.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #76	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@H]1O	5059.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #77	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@H]1O	5060.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #78	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	5074.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #79	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)O[C@@H]1CO	5055.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	5077.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #80	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5058.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #81	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@H]1O	5062.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #82	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5070.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #83	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5019.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #84	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5010.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #85	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5084.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #86	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	5066.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #87	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	5060.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #88	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	5069.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #89	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5029.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5091.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #90	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5022.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #91	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5097.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #92	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	5081.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #93	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	5072.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #94	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	5084.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #95	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5076.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #96	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5043.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #97	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	5019.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #98	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	5006.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,3TMS,isomer #99	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	5025.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4934.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #10	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4877.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #100	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4891.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #101	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4913.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #102	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4894.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #103	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4871.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #104	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4903.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #105	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4879.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #106	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4852.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #107	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4884.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #108	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4870.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #109	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4896.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4982.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #110	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4888.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #111	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4998.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #112	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4981.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #113	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5001.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #114	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	4968.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #115	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	5000.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #116	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4988.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #117	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4967.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #118	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4988.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #119	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4983.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4961.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #120	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4993.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #121	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4951.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #122	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4885.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #123	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4883.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #124	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4963.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #125	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4951.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #126	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	4941.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #127	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4959.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #128	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4905.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #129	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4903.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4981.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #130	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4989.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #131	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4975.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #132	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	4962.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #133	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4986.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #134	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4962.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #135	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4913.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #136	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4893.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #137	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	4881.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #138	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4902.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #139	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4910.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4955.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #140	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4892.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #141	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	4878.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #142	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4900.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #143	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C	4993.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #144	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	4990.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #145	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4998.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #146	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O[Si](C)(C)C	4986.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #147	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4986.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #148	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4988.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #149	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4914.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4983.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #150	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4899.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #151	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4921.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #152	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4932.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #153	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4887.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #154	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4888.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #155	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	4841.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #156	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O	4828.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #157	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	4842.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #158	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	4860.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #159	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	4933.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4950.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #160	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	4841.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #161	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)=CC=C1O	4829.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #162	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	4841.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #163	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	4858.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #164	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C=C12	4922.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #165	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C=C12	4927.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #166	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C=C12	4938.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #167	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O)C=C12	4931.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #168	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O[Si](C)(C)C)C=C12	4926.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #169	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=C12	4944.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4910.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #170	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4941.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #171	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4946.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #172	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4957.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #173	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4858.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #174	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4857.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #175	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4951.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #176	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4944.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #177	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4845.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #178	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4844.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #179	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4967.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4887.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #180	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4861.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #181	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4859.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #182	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4879.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #183	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4876.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #184	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4953.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #185	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O	4856.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #186	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	4860.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #187	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	4872.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #188	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	4926.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #189	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	4867.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4897.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #190	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	4860.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #191	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	4915.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #192	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C1O	4881.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #193	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O[Si](C)(C)C	4931.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #194	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	4944.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #195	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)=CC=C1O	4855.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #196	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	4860.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #197	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	4870.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #198	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	4866.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #199	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	4857.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4863.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4873.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #200	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC=C1O	4879.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #201	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)O[C@@H]1CO	4962.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #202	C[Si](C)(C)O[C@H]1[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4968.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #203	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@H]1O	4968.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #204	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@H]1O[Si](C)(C)C	4969.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #205	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4897.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #206	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4897.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #207	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4943.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #208	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4930.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #209	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4914.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4904.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #210	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4932.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #211	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4938.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #212	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4874.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #213	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4856.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #214	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4843.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #215	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4855.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #216	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4870.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #217	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4856.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #218	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4843.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #219	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4852.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #22	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4906.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #220	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4952.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #221	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4941.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #222	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4959.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #223	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4928.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #224	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4933.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #225	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	4929.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #226	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4957.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #227	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4891.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #228	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4874.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #229	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4861.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4885.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #230	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4871.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #231	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4887.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #232	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4873.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #233	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4861.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #234	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4870.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #235	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4975.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #236	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4962.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #237	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4986.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #238	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4947.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #239	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4952.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4893.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #240	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	4948.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #241	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	4955.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #242	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4937.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #243	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4924.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #244	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4942.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #245	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4889.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #246	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4876.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #247	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4896.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #248	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4869.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #249	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4874.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4868.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #250	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	4874.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #251	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	4886.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #252	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4871.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #253	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4893.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #254	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4864.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #255	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4869.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #256	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	4869.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #257	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4986.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #258	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)[C@@H]1O	4986.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #259	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	4987.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #26	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4899.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #260	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O	4965.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #261	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4909.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #262	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4911.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #263	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4925.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #264	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4873.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #265	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4876.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #266	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4914.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #267	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4910.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #268	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4861.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #269	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4863.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4991.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #270	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4932.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #271	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4872.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #272	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4873.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #273	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4892.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #274	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4892.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #275	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4979.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #276	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O	4840.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #277	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	4838.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #278	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	4853.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #279	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	4932.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #28	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4998.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #280	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	4842.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #281	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	4841.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #282	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	4920.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #283	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C1O	4856.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #284	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O[Si](C)(C)C	4928.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #285	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	4938.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #286	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)=CC=C1O	4840.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #287	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	4836.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #288	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	4852.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #289	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	4843.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #29	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4981.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #290	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	4840.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #291	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC=C1O	4853.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #292	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O)C=C12	4931.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #293	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O[Si](C)(C)C)C=C12	4943.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #294	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=C12	4947.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #295	C[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C=C12	4950.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #296	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4950.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #297	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4960.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #298	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4856.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #299	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4855.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4860.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #30	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	5001.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #300	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4966.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #301	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4855.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #302	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4852.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #303	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4866.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #304	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4865.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #305	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4947.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #306	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	4968.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #307	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4858.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #308	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4857.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #309	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4854.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #31	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4972.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #310	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4852.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #311	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4932.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #312	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)=[O+]C2=C1	4872.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #313	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4869.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #314	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4941.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #315	C[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C)C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=[O+]C2=C1	4957.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #316	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O)=CC=C1O	4870.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #317	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O[Si](C)(C)C)=CC=C1O	4872.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #318	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C	4926.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #319	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC=C1O	4877.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #32	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4958.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #320	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O[Si](C)(C)C	4929.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #321	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	4941.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #322	C[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC=C1O	4883.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #323	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O[Si](C)(C)C	4931.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #324	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	4931.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #325	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C1O[Si](C)(C)C	4947.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #326	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O)C=C1O	4873.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #327	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)[C@H]2O[Si](C)(C)C)C=C1O	4874.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #328	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C1O	4879.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #329	C[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C=C1O	4885.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #33	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4979.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #330	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@H]1O[Si](C)(C)C	4982.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #34	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4981.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #35	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	5002.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #36	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4999.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #37	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4887.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #38	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4886.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #39	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4941.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4957.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #40	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4924.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #41	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4929.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #42	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4910.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #43	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4937.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #44	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4933.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #45	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4869.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #46	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4852.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #47	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4853.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #48	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4839.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #49	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4864.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4936.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #50	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4867.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #51	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4852.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #52	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4852.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #53	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4838.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #54	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4863.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #55	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4958.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #56	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4952.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #57	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4930.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #58	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4956.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #59	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4941.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4958.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #60	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4916.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #61	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4943.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #62	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4928.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #63	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4955.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #64	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4948.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #65	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4950.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #66	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4892.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #67	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4872.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #68	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4868.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #69	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4858.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4935.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #70	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4884.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #71	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4889.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #72	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4871.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #73	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4866.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #74	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4857.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #75	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4882.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #76	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4984.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #77	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4973.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #78	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4950.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #79	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4978.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O[Si](C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4961.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #80	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4964.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #81	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4936.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #82	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4965.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #83	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4949.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #84	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4972.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #85	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4968.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #86	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4950.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #87	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4935.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #88	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4944.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #89	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4920.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	4880.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #90	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4950.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #91	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	4915.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #92	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4899.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #93	C[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)[C@@H]1O	4876.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #94	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO[Si](C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4907.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #95	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4881.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #96	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4856.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #97	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4887.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #98	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4873.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,4TMS,isomer #99	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4901.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5562.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@H]1O	5557.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #11	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@H]1O	5546.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	5548.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5575.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C=C12	5573.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5591.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	5560.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5570.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)O[C@H](CO)[C@@H](O)[C@@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	5581.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5557.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5605.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	5599.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O[Si](C)(C)C(C)(C)C	5608.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C=C12	5555.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5573.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5538.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	5528.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	5576.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5567.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@H]1O	5570.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	5578.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5562.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5572.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5587.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5553.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5540.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1O	5617.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)[C@@H]1O	5594.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O	5598.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=CC3=C(O)C=C(O)C=C3[O+]=C2C2=CC=C(O)C(O)=C2)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O	5598.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5570.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5553.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5578.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	5542.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C=C12	5547.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)[C@H]3O)C=C12	5547.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)[C@H]3O)C=C12	5556.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=[O+]C(C3=CC=C(O)C(O)=C3)=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C(C)(C)C)C=C12	5576.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5564.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5561.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)[C@H]3O)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5573.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)=[O+]C2=C1	5594.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=[O+]C2=C1	5567.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5542.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H]3O)C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=[O+]C2=C1	5560.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)=CC=C1O	5518.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)[C@H]2O)=CC=C1O	5515.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H]2O)=CC=C1O	5526.1	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1=CC(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C(C)(C)C)=CC=C1O	5546.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O)C=C1O[Si](C)(C)C(C)(C)C	5585.0	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)[C@H]2O)C=C1O	5526.3	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)[C@H]2O)C=C1O	5523.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #48	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)[C@H]2O)C=C1O	5536.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #49	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=[O+]C3=CC(O)=CC(O)=C3C=C2O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	5556.2	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5529.8	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #50	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@H]1O	5589.6	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #51	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@H]1O	5591.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #52	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5596.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #53	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@@H]1CO	5569.4	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #54	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)O[C@H](CO)[C@H]1O	5581.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #55	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5572.7	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O	5611.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@@H]1O	5583.9	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	5598.5	Semi standard non polar	33892256
Cyanidin 3-laminaribioside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](OC3=CC4=C(O)C=C(O)C=C4[O+]=C3C3=CC=C(O)C(O)=C3)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	5594.5	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (Non-derivatized) - 70eV, Positive	splash10-0f9y-2251090000-b4a9ffbf2d2df8b39b41	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (1 TMS) - 70eV, Positive	splash10-00xr-8208109000-7a57c54e29e834b36453	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_1_11) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Cyanidin 3-laminaribioside GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-laminaribioside 10V, Positive-QTOF	splash10-03di-0101009000-a453d661e22488349e75	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-laminaribioside 20V, Positive-QTOF	splash10-06r6-2602089000-29b17ae5f9882a71f652	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-laminaribioside 40V, Positive-QTOF	splash10-03dm-4901000000-0b10c22d8b35e4e96aa8	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-laminaribioside 10V, Negative-QTOF	splash10-03di-1321009000-3eb9a811a126ef651fb5	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-laminaribioside 20V, Negative-QTOF	splash10-08i0-4911004000-9988b85c4b13490a6d56	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-laminaribioside 40V, Negative-QTOF	splash10-002f-8900000000-66b5962b182260419517	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-laminaribioside 10V, Positive-QTOF	splash10-0udi-0110922000-6257eb152993a8a52b5a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-laminaribioside 20V, Positive-QTOF	splash10-0f8i-0321910000-6613861638615028e423	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Cyanidin 3-laminaribioside 40V, Positive-QTOF	splash10-01pa-2791100000-c263160d38b3fac1977c	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

FooDB ID

FDB017190

KNApSAcK ID

C00006659

Chemspider ID

30777224

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101710212

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Showing metabocard for Cyanidin 3-laminaribioside (HMDB0037996)

MOL for HMDB0037996 (Cyanidin 3-laminaribioside)

3D MOL for HMDB0037996 (Cyanidin 3-laminaribioside)

3D SDF for HMDB0037996 (Cyanidin 3-laminaribioside)

3D-SDF for HMDB0037996 (Cyanidin 3-laminaribioside)

PDB for HMDB0037996 (Cyanidin 3-laminaribioside)

3D PDB for HMDB0037996 (Cyanidin 3-laminaribioside)

SMILES for HMDB0037996 (Cyanidin 3-laminaribioside)

INCHI for HMDB0037996 (Cyanidin 3-laminaribioside)

Structure for HMDB0037996 (Cyanidin 3-laminaribioside)

3D Structure for HMDB0037996 (Cyanidin 3-laminaribioside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra