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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:51:38 UTC

Update Date

2022-03-07 02:53:27 UTC

HMDB ID

HMDB0032762

Secondary Accession Numbers

HMDB32762

Metabolite Identification

Common Name

Leucodelphinidin 3-[galactosyl-(1->4)-glucoside]

Description

Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] has been detected, but not quantified in, a few different foods, such as fats and oils, green vegetables, and herbs and spices. This could make leucodelphinidin 3-[galactosyl-(1->4)-glucoside] a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Leucodelphinidin 3-[galactosyl-(1->4)-glucoside].

Structure

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


  Mrv0541 05061306402D          

 45 49  0  0  0  0            999 V2000
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  2  0  0  0  0
  7  2  1  0  0  0  0
  8  3  2  0  0  0  0
  8  4  1  0  0  0  0
  9  3  1  0  0  0  0
 10  1  1  0  0  0  0
 11  2  2  0  0  0  0
 12  4  2  0  0  0  0
 13  5  1  0  0  0  0
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 15  9  2  0  0  0  0
 15 12  1  0  0  0  0
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 17 13  1  0  0  0  0
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 23  7  1  0  0  0  0
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 34 16  1  0  0  0  0
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 38 20  1  0  0  0  0
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 41 12  1  0  0  0  0
 41 23  1  0  0  0  0
 42 13  1  0  0  0  0
 42 26  1  0  0  0  0
 43 14  1  0  0  0  0
 43 27  1  0  0  0  0
 44 24  1  0  0  0  0
 44 26  1  0  0  0  0
 45 25  1  0  0  0  0
 45 27  1  0  0  0  0
M  END

HMDB0032762
     RDKit          3D
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside]
 79 83  0  0  0  0  0  0  0  0999 V2000
   -7.1999   -2.0388   -0.1428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8050   -0.8934   -0.8027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7260   -0.2126    0.0237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3531    0.9269   -0.6630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3799    1.6766    0.0022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1573    1.0406    0.0067 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1934    1.7480   -0.7099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7239    0.8782   -1.8124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0578    1.5566   -3.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2302    2.6736   -3.2393 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4096    0.5410   -1.8615 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2885    0.5586   -0.6749 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5410    0.0548   -0.8943 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9307   -0.9886   -0.1017 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1834   -2.2621   -0.7764 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0896   -3.0365   -1.1978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1777   -2.5322   -0.9625 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3155   -4.2537   -1.8238 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5917   -4.7247   -2.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6469   -3.9504   -1.6247 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4589   -2.7052   -0.9832 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5382   -1.9641   -0.5794 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3698   -0.6519   -0.1123 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5611   -0.2146    0.6127 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5330    0.3938    1.8318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7033    0.8062    2.4943 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6083    1.4190    3.7307 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9339    0.6055    1.9244 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1182    0.9875    2.5235 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9654   -0.0207    0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2210   -0.2152    0.1091 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8054   -0.4156    0.0411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1346   -0.6512    0.7880 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3305   -1.6540    1.7308 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2667    2.0184   -0.2253 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1049    2.2883    0.8235 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2805    3.6051    0.5222 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7995    2.0165    1.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9020    2.8679    1.3541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2317    0.7855    2.1859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7142    1.2128    3.4220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3326    0.1105    1.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4107    0.9700    1.2702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4702   -2.7270   -0.8070 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8649   -0.8710    0.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2849    2.6196   -0.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7056    2.6640   -1.1064 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7820    0.8976   -4.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7106    3.4733   -3.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1919   -0.0207    0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0751   -1.1860    0.6108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9912   -3.0700   -1.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4386   -4.8130   -2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9873   -6.5166   -2.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6664   -4.2925   -1.7832 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1233    0.0500   -0.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6023    0.5818    2.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4400    1.7125    4.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2460    1.4357    3.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2507   -0.6656   -0.7972 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9112   -0.8990   -0.9387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9707    0.3409    1.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5823   -1.6028    2.3797 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7646    3.0842    1.2992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2430    1.6944    1.2232 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.3121    0.4963    3.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6278   -0.8625    1.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4793    1.4235    0.4145 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
  9 10  1  0
  8 11  1  0
 11 12  1  0
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 13 14  1  0
 14 15  1  0
 15 16  2  0
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 19 20  1  0
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 21 22  2  0
 22 23  1  0
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 24 25  1  0
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 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  2  0
 24 34  1  0
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  5 40  1  0
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 36 70  1  0
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 38 72  1  0
 39 73  1  0
 40 74  1  0
 41 75  1  0
 42 76  1  0
 43 77  1  0
 44 78  1  0
 45 79  1  0
M  END


  Mrv0541 05061306402D          

 45 49  0  0  0  0            999 V2000
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  2  0  0  0  0
  7  2  1  0  0  0  0
  8  3  2  0  0  0  0
  8  4  1  0  0  0  0
  9  3  1  0  0  0  0
 10  1  1  0  0  0  0
 11  2  2  0  0  0  0
 12  4  2  0  0  0  0
 13  5  1  0  0  0  0
 14  6  1  0  0  0  0
 15  9  2  0  0  0  0
 15 12  1  0  0  0  0
 16 10  2  0  0  0  0
 16 11  1  0  0  0  0
 17 13  1  0  0  0  0
 18 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 19  1  0  0  0  0
 23  7  1  0  0  0  0
 23 22  1  0  0  0  0
 24 14  1  0  0  0  0
 24 19  1  0  0  0  0
 25 15  1  0  0  0  0
 25 22  1  0  0  0  0
 26 20  1  0  0  0  0
 27 21  1  0  0  0  0
 28  5  1  0  0  0  0
 29  6  1  0  0  0  0
 30  8  1  0  0  0  0
 31  9  1  0  0  0  0
 32 10  1  0  0  0  0
 33 11  1  0  0  0  0
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 35 17  1  0  0  0  0
 36 18  1  0  0  0  0
 37 19  1  0  0  0  0
 38 20  1  0  0  0  0
 39 21  1  0  0  0  0
 40 22  1  0  0  0  0
 41 12  1  0  0  0  0
 41 23  1  0  0  0  0
 42 13  1  0  0  0  0
 42 26  1  0  0  0  0
 43 14  1  0  0  0  0
 43 27  1  0  0  0  0
 44 24  1  0  0  0  0
 44 26  1  0  0  0  0
 45 25  1  0  0  0  0
 45 27  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0032762

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(OC2C(O)C(O)C(OC3C(O)C(OC4=CC(O)=CC(O)=C34)C3=CC(O)=C(O)C(O)=C3)OC2CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O18/c28-5-13-17(35)18(36)20(38)26(42-13)44-24-14(6-29)43-27(21(39)19(24)37)45-25-15-9(31)3-8(30)4-12(15)41-23(22(25)40)7-1-10(32)16(34)11(33)2-7/h1-4,13-14,17-40H,5-6H2

> <INCHI_KEY>
QDZRWBGIKIHOHH-UHFFFAOYSA-N

> <FORMULA>
C27H34O18

> <MOLECULAR_WEIGHT>
646.5481

> <EXACT_MASS>
646.174514284

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_AVERAGE_POLARIZABILITY>
60.613662629171586

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-{[3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

> <ALOGPS_LOGP>
-1.08

> <JCHEM_LOGP>
-2.9691257446666657

> <ALOGPS_LOGS>
-1.54

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.152791298511639

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.560853569062557

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7164888791870814

> <JCHEM_POLAR_SURFACE_AREA>
309.14000000000004

> <JCHEM_REFRACTIVITY>
142.0147

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.86e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{[3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0032762
     RDKit          3D
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside]
 79 83  0  0  0  0  0  0  0  0999 V2000
   -7.1999   -2.0388   -0.1428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8050   -0.8934   -0.8027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7260   -0.2126    0.0237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3531    0.9269   -0.6630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3799    1.6766    0.0022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1573    1.0406    0.0067 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1934    1.7480   -0.7099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7239    0.8782   -1.8124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0578    1.5566   -3.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2302    2.6736   -3.2393 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4096    0.5410   -1.8615 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2885    0.5586   -0.6749 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5410    0.0548   -0.8943 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1834   -2.2621   -0.7764 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0896   -3.0365   -1.1978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1777   -2.5322   -0.9625 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3155   -4.2537   -1.8238 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5917   -4.7247   -2.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6469   -3.9504   -1.6247 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5382   -1.9641   -0.5794 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5611   -0.2146    0.6127 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5330    0.3938    1.8318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7033    0.8062    2.4943 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6083    1.4190    3.7307 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9339    0.6055    1.9244 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1182    0.9875    2.5235 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9654   -0.0207    0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2210   -0.2152    0.1091 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8054   -0.4156    0.0411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1346   -0.6512    0.7880 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3305   -1.6540    1.7308 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2667    2.0184   -0.2253 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1049    2.2883    0.8235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1554    2.2458    0.2419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2805    3.6051    0.5222 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7995    2.0165    1.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9020    2.8679    1.3541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2317    0.7855    2.1859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7142    1.2128    3.4220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3326    0.1105    1.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4107    0.9700    1.2702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4702   -2.7270   -0.8070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6844   -0.2365   -0.9384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4132   -1.1805   -1.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8649   -0.8710    0.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2849    2.6196   -0.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7056    2.6640   -1.1064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3015   -0.0950   -1.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1216    1.8082   -3.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7820    0.8976   -4.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7106    3.4733   -3.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1919   -0.0207    0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0751   -1.1860    0.6108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9912   -3.0700   -1.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4386   -4.8130   -2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9873   -6.5166   -2.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6664   -4.2925   -1.7832 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1233    0.0500   -0.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6023    0.5818    2.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4400    1.7125    4.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2460    1.4357    3.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2507   -0.6656   -0.7972 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9112   -0.8990   -0.9387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9707    0.3409    1.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5823   -1.6028    2.3797 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5105    2.6405   -1.1214 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7646    3.0842    1.2992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2430    1.6944    1.2232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4751    3.7799    1.4866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9673    2.5513    1.8863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2976    3.0289    2.2425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3872    0.0965    2.2805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3121    0.4963    3.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6278   -0.8625    1.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4793    1.4235    0.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
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 44 78  1  0
 45 79  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      12.003  -2.310   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      13.337  -4.620   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      13.337  -7.700   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      10.669  -9.240   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    7   10                                                       
CONECT    2    7   11                                                       
CONECT    3    8    9                                                       
CONECT    4    8   12                                                       
CONECT    5   13   28                                                       
CONECT    6   14   29                                                       
CONECT    7    1    2   23                                                  
CONECT    8    3    4   30                                                  
CONECT    9    3   15   31                                                  
CONECT   10    1   16   32                                                  
CONECT   11    2   16   33                                                  
CONECT   12    4   15   41                                                  
CONECT   13    5   17   42                                                  
CONECT   14    6   24   43                                                  
CONECT   15    9   12   25                                                  
CONECT   16   10   11   34                                                  
CONECT   17   13   18   35                                                  
CONECT   18   17   20   36                                                  
CONECT   19   21   24   37                                                  
CONECT   20   18   26   38                                                  
CONECT   21   19   27   39                                                  
CONECT   22   23   25   40                                                  
CONECT   23    7   22   41                                                  
CONECT   24   14   19   44                                                  
CONECT   25   15   22   45                                                  
CONECT   26   20   42   44                                                  
CONECT   27   21   43   45                                                  
CONECT   28    5                                                            
CONECT   29    6                                                            
CONECT   30    8                                                            
CONECT   31    9                                                            
CONECT   32   10                                                            
CONECT   33   11                                                            
CONECT   34   16                                                            
CONECT   35   17                                                            
CONECT   36   18                                                            
CONECT   37   19                                                            
CONECT   38   20                                                            
CONECT   39   21                                                            
CONECT   40   22                                                            
CONECT   41   12   23                                                       
CONECT   42   13   26                                                       
CONECT   43   14   27                                                       
CONECT   44   24   26                                                       
CONECT   45   25   27                                                       
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

COMPND    HMDB0032762
HETATM    1  O1  UNL     1      -7.200  -2.039  -0.143  1.00  0.00           O  
HETATM    2  C1  UNL     1      -6.805  -0.893  -0.803  1.00  0.00           C  
HETATM    3  C2  UNL     1      -5.726  -0.213   0.024  1.00  0.00           C  
HETATM    4  O2  UNL     1      -5.353   0.927  -0.663  1.00  0.00           O  
HETATM    5  C3  UNL     1      -4.380   1.677   0.002  1.00  0.00           C  
HETATM    6  O3  UNL     1      -3.157   1.041   0.007  1.00  0.00           O  
HETATM    7  C4  UNL     1      -2.193   1.748  -0.710  1.00  0.00           C  
HETATM    8  C5  UNL     1      -1.724   0.878  -1.812  1.00  0.00           C  
HETATM    9  C6  UNL     1      -2.058   1.557  -3.151  1.00  0.00           C  
HETATM   10  O4  UNL     1      -1.230   2.674  -3.239  1.00  0.00           O  
HETATM   11  O5  UNL     1      -0.410   0.541  -1.861  1.00  0.00           O  
HETATM   12  C7  UNL     1       0.289   0.559  -0.675  1.00  0.00           C  
HETATM   13  O6  UNL     1       1.541   0.055  -0.894  1.00  0.00           O  
HETATM   14  C8  UNL     1       1.931  -0.989  -0.102  1.00  0.00           C  
HETATM   15  C9  UNL     1       2.183  -2.262  -0.776  1.00  0.00           C  
HETATM   16  C10 UNL     1       1.090  -3.037  -1.198  1.00  0.00           C  
HETATM   17  O7  UNL     1      -0.178  -2.532  -0.963  1.00  0.00           O  
HETATM   18  C11 UNL     1       1.316  -4.254  -1.824  1.00  0.00           C  
HETATM   19  C12 UNL     1       2.592  -4.725  -2.045  1.00  0.00           C  
HETATM   20  O8  UNL     1       2.742  -5.943  -2.672  1.00  0.00           O  
HETATM   21  C13 UNL     1       3.647  -3.950  -1.625  1.00  0.00           C  
HETATM   22  C14 UNL     1       3.459  -2.705  -0.983  1.00  0.00           C  
HETATM   23  O9  UNL     1       4.538  -1.964  -0.579  1.00  0.00           O  
HETATM   24  C15 UNL     1       4.370  -0.652  -0.112  1.00  0.00           C  
HETATM   25  C16 UNL     1       5.561  -0.215   0.613  1.00  0.00           C  
HETATM   26  C17 UNL     1       5.533   0.394   1.832  1.00  0.00           C  
HETATM   27  C18 UNL     1       6.703   0.806   2.494  1.00  0.00           C  
HETATM   28  O10 UNL     1       6.608   1.419   3.731  1.00  0.00           O  
HETATM   29  C19 UNL     1       7.934   0.606   1.924  1.00  0.00           C  
HETATM   30  O11 UNL     1       9.118   0.988   2.524  1.00  0.00           O  
HETATM   31  C20 UNL     1       7.965  -0.021   0.670  1.00  0.00           C  
HETATM   32  O12 UNL     1       9.221  -0.215   0.109  1.00  0.00           O  
HETATM   33  C21 UNL     1       6.805  -0.416   0.041  1.00  0.00           C  
HETATM   34  C22 UNL     1       3.135  -0.651   0.788  1.00  0.00           C  
HETATM   35  O13 UNL     1       3.331  -1.654   1.731  1.00  0.00           O  
HETATM   36  C23 UNL     1       0.267   2.018  -0.225  1.00  0.00           C  
HETATM   37  O14 UNL     1       1.105   2.288   0.824  1.00  0.00           O  
HETATM   38  C24 UNL     1      -1.155   2.246   0.242  1.00  0.00           C  
HETATM   39  O15 UNL     1      -1.280   3.605   0.522  1.00  0.00           O  
HETATM   40  C25 UNL     1      -4.799   2.017   1.403  1.00  0.00           C  
HETATM   41  O16 UNL     1      -5.902   2.868   1.354  1.00  0.00           O  
HETATM   42  C26 UNL     1      -5.232   0.786   2.186  1.00  0.00           C  
HETATM   43  O17 UNL     1      -5.714   1.213   3.422  1.00  0.00           O  
HETATM   44  C27 UNL     1      -6.333   0.110   1.378  1.00  0.00           C  
HETATM   45  O18 UNL     1      -7.411   0.970   1.270  1.00  0.00           O  
HETATM   46  H1  UNL     1      -7.470  -2.727  -0.807  1.00  0.00           H  
HETATM   47  H2  UNL     1      -7.684  -0.236  -0.938  1.00  0.00           H  
HETATM   48  H3  UNL     1      -6.413  -1.180  -1.811  1.00  0.00           H  
HETATM   49  H4  UNL     1      -4.865  -0.871   0.199  1.00  0.00           H  
HETATM   50  H5  UNL     1      -4.285   2.620  -0.571  1.00  0.00           H  
HETATM   51  H6  UNL     1      -2.706   2.664  -1.106  1.00  0.00           H  
HETATM   52  H7  UNL     1      -2.301  -0.095  -1.870  1.00  0.00           H  
HETATM   53  H8  UNL     1      -3.122   1.808  -3.233  1.00  0.00           H  
HETATM   54  H9  UNL     1      -1.782   0.898  -4.010  1.00  0.00           H  
HETATM   55  H10 UNL     1      -1.711   3.473  -3.582  1.00  0.00           H  
HETATM   56  H11 UNL     1      -0.192  -0.021   0.148  1.00  0.00           H  
HETATM   57  H12 UNL     1       1.075  -1.186   0.611  1.00  0.00           H  
HETATM   58  H13 UNL     1      -0.991  -3.070  -1.224  1.00  0.00           H  
HETATM   59  H14 UNL     1       0.439  -4.813  -2.130  1.00  0.00           H  
HETATM   60  H15 UNL     1       1.987  -6.517  -2.983  1.00  0.00           H  
HETATM   61  H16 UNL     1       4.666  -4.292  -1.783  1.00  0.00           H  
HETATM   62  H17 UNL     1       4.123   0.050  -0.953  1.00  0.00           H  
HETATM   63  H18 UNL     1       4.602   0.582   2.339  1.00  0.00           H  
HETATM   64  H19 UNL     1       7.440   1.712   4.201  1.00  0.00           H  
HETATM   65  H20 UNL     1       9.246   1.436   3.402  1.00  0.00           H  
HETATM   66  H21 UNL     1       9.251  -0.666  -0.797  1.00  0.00           H  
HETATM   67  H22 UNL     1       6.911  -0.899  -0.939  1.00  0.00           H  
HETATM   68  H23 UNL     1       2.971   0.341   1.198  1.00  0.00           H  
HETATM   69  H24 UNL     1       2.582  -1.603   2.380  1.00  0.00           H  
HETATM   70  H25 UNL     1       0.510   2.641  -1.121  1.00  0.00           H  
HETATM   71  H26 UNL     1       0.765   3.084   1.299  1.00  0.00           H  
HETATM   72  H27 UNL     1      -1.243   1.694   1.223  1.00  0.00           H  
HETATM   73  H28 UNL     1      -1.475   3.780   1.487  1.00  0.00           H  
HETATM   74  H29 UNL     1      -3.967   2.551   1.886  1.00  0.00           H  
HETATM   75  H30 UNL     1      -6.298   3.029   2.243  1.00  0.00           H  
HETATM   76  H31 UNL     1      -4.387   0.096   2.281  1.00  0.00           H  
HETATM   77  H32 UNL     1      -6.312   0.496   3.764  1.00  0.00           H  
HETATM   78  H33 UNL     1      -6.628  -0.863   1.826  1.00  0.00           H  
HETATM   79  H34 UNL     1      -7.479   1.424   0.414  1.00  0.00           H  
CONECT    1    2   46
CONECT    2    3   47   48
CONECT    3    4   44   49
CONECT    4    5
CONECT    5    6   40   50
CONECT    6    7
CONECT    7    8   38   51
CONECT    8    9   11   52
CONECT    9   10   53   54
CONECT   10   55
CONECT   11   12
CONECT   12   13   36   56
CONECT   13   14
CONECT   14   15   34   57
CONECT   15   16   16   22
CONECT   16   17   18
CONECT   17   58
CONECT   18   19   19   59
CONECT   19   20   21
CONECT   20   60
CONECT   21   22   22   61
CONECT   22   23
CONECT   23   24
CONECT   24   25   34   62
CONECT   25   26   26   33
CONECT   26   27   63
CONECT   27   28   29   29
CONECT   28   64
CONECT   29   30   31
CONECT   30   65
CONECT   31   32   33   33
CONECT   32   66
CONECT   33   67
CONECT   34   35   68
CONECT   35   69
CONECT   36   37   38   70
CONECT   37   71
CONECT   38   39   72
CONECT   39   73
CONECT   40   41   42   74
CONECT   41   75
CONECT   42   43   44   76
CONECT   43   77
CONECT   44   45   78
CONECT   45   79
END

HMDB0032762
     RDKit          3D
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside]
 79 83  0  0  0  0  0  0  0  0999 V2000
   -7.1999   -2.0388   -0.1428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8050   -0.8934   -0.8027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7260   -0.2126    0.0237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3531    0.9269   -0.6630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3799    1.6766    0.0022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1573    1.0406    0.0067 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1934    1.7480   -0.7099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7239    0.8782   -1.8124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0578    1.5566   -3.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2302    2.6736   -3.2393 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4096    0.5410   -1.8615 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2885    0.5586   -0.6749 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5410    0.0548   -0.8943 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9307   -0.9886   -0.1017 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1834   -2.2621   -0.7764 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0896   -3.0365   -1.1978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1777   -2.5322   -0.9625 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3155   -4.2537   -1.8238 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5917   -4.7247   -2.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7417   -5.9428   -2.6719 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6469   -3.9504   -1.6247 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4589   -2.7052   -0.9832 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5382   -1.9641   -0.5794 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3698   -0.6519   -0.1123 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5611   -0.2146    0.6127 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5330    0.3938    1.8318 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7033    0.8062    2.4943 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6083    1.4190    3.7307 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9339    0.6055    1.9244 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1182    0.9875    2.5235 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9654   -0.0207    0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2210   -0.2152    0.1091 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8054   -0.4156    0.0411 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1346   -0.6512    0.7880 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3305   -1.6540    1.7308 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2667    2.0184   -0.2253 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1049    2.2883    0.8235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1554    2.2458    0.2419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2805    3.6051    0.5222 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7995    2.0165    1.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9020    2.8679    1.3541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2317    0.7855    2.1859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7142    1.2128    3.4220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3326    0.1105    1.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4107    0.9700    1.2702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4702   -2.7270   -0.8070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6844   -0.2365   -0.9384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4132   -1.1805   -1.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8649   -0.8710    0.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2849    2.6196   -0.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7056    2.6640   -1.1064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3015   -0.0950   -1.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1216    1.8082   -3.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7820    0.8976   -4.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7106    3.4733   -3.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1919   -0.0207    0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0751   -1.1860    0.6108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9912   -3.0700   -1.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4386   -4.8130   -2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9873   -6.5166   -2.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6664   -4.2925   -1.7832 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1233    0.0500   -0.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6023    0.5818    2.3390 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4400    1.7125    4.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2460    1.4357    3.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2507   -0.6656   -0.7972 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9112   -0.8990   -0.9387 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9707    0.3409    1.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5823   -1.6028    2.3797 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5105    2.6405   -1.1214 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7646    3.0842    1.2992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2430    1.6944    1.2232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4751    3.7799    1.4866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9673    2.5513    1.8863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2976    3.0289    2.2425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3872    0.0965    2.2805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3121    0.4963    3.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6278   -0.8625    1.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4793    1.4235    0.4145 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
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  8 11  1  0
 11 12  1  0
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 22 23  1  0
 23 24  1  0
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 26 27  1  0
 27 28  1  0
 27 29  2  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  2  0
 24 34  1  0
 34 35  1  0
 12 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
  5 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 42 44  1  0
 44 45  1  0
 44  3  1  0
 38  7  1  0
 34 14  1  0
 22 15  1  0
 33 25  1  0
  1 46  1  0
  2 47  1  0
  2 48  1  0
  3 49  1  0
  5 50  1  0
  7 51  1  0
  8 52  1  0
  9 53  1  0
  9 54  1  0
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 17 58  1  0
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 35 69  1  0
 36 70  1  0
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 45 79  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₇H₃₄O₁₈

Average Molecular Weight

646.5481

Monoisotopic Molecular Weight

646.174514284

IUPAC Name

4-{[3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

Traditional Name

4-{[3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

CAS Registry Number

189890-19-5

SMILES

OCC1OC(OC2C(O)C(O)C(OC3C(O)C(OC4=CC(O)=CC(O)=C34)C3=CC(O)=C(O)C(O)=C3)OC2CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C27H34O18/c28-5-13-17(35)18(36)20(38)26(42-13)44-24-14(6-29)43-27(21(39)19(24)37)45-25-15-9(31)3-8(30)4-12(15)41-23(22(25)40)7-1-10(32)16(34)11(33)2-7/h1-4,13-14,17-40H,5-6H2

InChI Key

QDZRWBGIKIHOHH-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid O-glycosides

Alternative Parents

Substituents

Flavonoid o-glycoside
Epigallocatechin
Catechin
Leucoanthocyanidin-skeleton
5-hydroxyflavonoid
7-hydroxyflavonoid
3-hydroxyflavonoid
3'-hydroxyflavonoid
Hydroxyflavonoid
4'-hydroxyflavonoid
Flavan
Disaccharide
Glycosyl compound
O-glycosyl compound
Chromane
Benzopyran
1-benzopyran
Benzenetriol
Pyrogallol derivative
Phenol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Oxane
Monocyclic benzene moiety
Benzenoid
Secondary alcohol
Ether
Acetal
Oxacycle
Polyol
Organoheterocyclic compound
Organooxygen compound
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0032762)
Cytoplasm (HMDB: HMDB0032762)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0032762)

Source

Exogenous

Food

Food (HMDB: HMDB0032762)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Vegetable

Leaf vegetable

Green vegetables (FooDB: FOOD00872)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Endogenous

Plant

Plant (HMDB: HMDB0032762)

Not Available

Nutrient (HMDB: HMDB0032762)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	158 °C	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	18.6 g/L	ALOGPS
logP	-1.1	ALOGPS
logP	-3	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	8.56	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	309.14 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	142.01 m³·mol⁻¹	ChemAxon
Polarizability	60.61 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
DarkChem	[M+H]+	243.135	31661259
DarkChem	[M-H]-	234.361	31661259
DeepCCS	[M-2H]-	265.956	30932474
DeepCCS	[M+Na]+	240.24	30932474
AllCCS	[M+H]+	236.4	32859911
AllCCS	[M+H-H2O]+	235.5	32859911
AllCCS	[M+NH4]+	237.2	32859911
AllCCS	[M+Na]+	237.5	32859911
AllCCS	[M-H]-	233.5	32859911
AllCCS	[M+Na-2H]-	236.1	32859911
AllCCS	[M+HCOO]-	239.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside]	OCC1OC(OC2C(O)C(O)C(OC3C(O)C(OC4=CC(O)=CC(O)=C34)C3=CC(O)=C(O)C(O)=C3)OC2CO)C(O)C(O)C1O	6160.4	Standard polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside]	OCC1OC(OC2C(O)C(O)C(OC3C(O)C(OC4=CC(O)=CC(O)=C34)C3=CC(O)=C(O)C(O)=C3)OC2CO)C(O)C(O)C1O	5612.3	Standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside]	OCC1OC(OC2C(O)C(O)C(OC3C(O)C(OC4=CC(O)=CC(O)=C34)C3=CC(O)=C(O)C(O)=C3)OC2CO)C(O)C(O)C1O	5943.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5824.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #10	C[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)OC(CO)C(O)C1O	5889.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #11	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C1O	5881.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #12	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C1O	5889.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #2	C[Si](C)(C)OC1C(O)C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C1OC1OC(CO)C(O)C(O)C1O	5887.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #3	C[Si](C)(C)OC1C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C1O	5874.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #4	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5869.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #5	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5928.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #6	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5934.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #7	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O	5900.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #8	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)C=C1O	5906.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5838.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5772.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	5782.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	5784.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #12	C[Si](C)(C)OC1C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C	5828.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #13	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5856.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #14	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5854.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #15	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)C3O)C2O)=CC(O)=C1O	5805.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #16	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)C3O)C2O)C=C1O	5794.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #17	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5807.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	5788.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #19	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C1O	5814.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5815.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #20	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C1O	5810.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #21	C[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)OC(CO)C(O)C1O	5814.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #22	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O[Si](C)(C)C)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5843.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #23	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5841.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #24	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O[Si](C)(C)C)C2O)=CC(O)=C1O	5795.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #25	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O[Si](C)(C)C)C2O)C=C1O	5784.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #26	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5804.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O[Si](C)(C)C)C(O)C1OC1OC(CO)C(O)C(O)C1O	5778.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #28	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O)C1O	5805.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #29	C[Si](C)(C)OC1C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C1O	5800.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5809.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #30	C[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)OC(CO)C(O)C1O	5806.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #31	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O[Si](C)(C)C)=CC(O)=C1O	5798.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #32	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O[Si](C)(C)C)C=C1O	5792.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #33	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5837.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #34	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5834.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5784.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #36	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5801.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #37	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5797.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #38	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5802.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #39	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5835.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5773.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #40	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5825.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #41	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5818.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #42	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5823.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #43	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5846.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #44	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5839.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #45	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5845.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #46	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5829.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #47	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5847.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #48	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5835.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #49	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5844.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5771.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #50	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O	5829.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #51	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5817.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #52	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5786.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #53	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O	5799.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #54	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)C3O)C2O)=CC(O)=C1O	5786.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #55	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)C3O)C2O)=CC(O)=C1O	5795.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #56	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O[Si](C)(C)C)=C1O	5785.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #57	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O[Si](C)(C)C	5764.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #58	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5784.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #59	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)C3O)C2O)C=C1O	5786.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	5772.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #60	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)C3O)C2O)C=C1O	5762.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #61	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)C3O)C2O)C=C1O	5782.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #62	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O	5792.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #63	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O	5791.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #64	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C	5793.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #65	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C1O	5795.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #66	C[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C	5815.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #67	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C1O[Si](C)(C)C	5809.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	5773.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	5783.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	5785.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5741.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	5733.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #100	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5719.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #101	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5733.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #102	C[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)OC(CO)C(O)C1O[Si](C)(C)C	5737.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #103	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O[Si](C)(C)C)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5743.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #104	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O[Si](C)(C)C)C(O)C1OC1OC(CO)C(O)C(O)C1O	5733.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #105	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)C1O[Si](C)(C)C)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5746.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #106	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)C1O[Si](C)(C)C)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5717.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #107	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5740.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #108	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O[Si](C)(C)C)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5735.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #109	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O[Si](C)(C)C)C2O)=CC(O)=C1O	5700.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5731.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #110	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O[Si](C)(C)C)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5672.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #111	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5714.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #112	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5684.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #113	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5759.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #114	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O[Si](C)(C)C)C(O)C1OC1OC(CO)C(O)C(O)C1O	5751.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #115	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5765.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #116	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5742.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #117	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5763.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #118	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C(O[Si](C)(C)C)C(O)C1OC1OC(CO)C(O)C(O)C1O	5689.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #119	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)C3O[Si](C)(C)C)C2O)=CC(O)=C1O	5690.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5689.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #120	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)C3O[Si](C)(C)C)C2O)=CC(O)=C1O	5657.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #121	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C2O)=CC(O)=C1O	5684.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #122	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O[Si](C)(C)C)C2O[Si](C)(C)C)=CC(O)=C1O	5704.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #123	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O[Si](C)(C)C)C2O)=CC(O[Si](C)(C)C)=C1O	5664.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #124	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O[Si](C)(C)C)C2O)=CC(O)=C1O[Si](C)(C)C	5651.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #125	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C(O[Si](C)(C)C)C(O)C1OC1OC(CO)C(O)C(O)C1O	5666.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #126	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)C3O[Si](C)(C)C)C2O)C=C1O	5663.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #127	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)C3O[Si](C)(C)C)C2O)C=C1O	5620.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #128	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C2O)C=C1O	5654.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #129	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1O	5687.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5653.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #130	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1OC1OC(CO)C(O)C(O)C1O	5726.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #131	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5727.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #132	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5715.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #133	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5730.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #134	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O[Si](C)(C)C)C(O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O	5733.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #135	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O[Si](C)(C)C)C(O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O	5715.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #136	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O[Si](C)(C)C)C(O)C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C	5733.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #137	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5714.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #138	C[Si](C)(C)OC1C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C1O	5728.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #139	C[Si](C)(C)OC1C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	5730.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	5733.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #140	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5732.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #141	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O[Si](C)(C)C)=CC(O)=C1O	5712.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #142	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5715.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #143	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)C3O)C2O[Si](C)(C)C)=CC(O)=C1O	5702.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #144	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)C3O)C2O[Si](C)(C)C)=CC(O)=C1O	5672.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #145	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)C3O)C2O[Si](C)(C)C)=CC(O)=C1O	5697.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #146	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5686.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #147	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5671.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #148	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5704.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #149	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O[Si](C)(C)C)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5684.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	5726.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #150	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5696.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #151	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)C3O)C2O[Si](C)(C)C)C=C1O	5675.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #152	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)C3O)C2O[Si](C)(C)C)C=C1O	5636.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #153	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)C3O)C2O[Si](C)(C)C)C=C1O	5667.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #154	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5744.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #155	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5763.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #156	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5763.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #157	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5746.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #158	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5760.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #159	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5744.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	5733.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #160	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)C1O)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5740.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #161	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)C1O)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5715.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #162	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)C1O)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5735.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #163	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C(O)C(O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O	5737.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #164	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C(O)C(O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O	5724.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #165	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C	5738.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #166	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5726.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #167	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5711.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #168	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5729.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #169	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5742.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	5742.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #170	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5751.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #171	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5720.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #172	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5742.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #173	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5691.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #174	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5666.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #175	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5680.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #176	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5663.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #177	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5710.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #178	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5708.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #179	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5670.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	5716.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #180	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5707.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #181	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5678.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #182	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5674.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #183	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5638.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #184	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5673.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #185	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O	5762.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #186	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O	5740.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #187	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C	5761.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #188	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5761.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #189	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5750.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	5736.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #190	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5767.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #191	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5707.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #192	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5672.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #193	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O	5753.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #194	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O	5725.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #195	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C	5746.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #196	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5740.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #197	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5730.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #198	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O	5694.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #199	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5663.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5750.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5694.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #200	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5746.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #201	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)C3O)C2O)=CC(O)=C1O	5650.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #202	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5619.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #203	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)C3O)C2O)=CC(O)=C1O	5691.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #204	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)C1O)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5658.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #205	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O[Si](C)(C)C)=C1O	5671.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #206	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O[Si](C)(C)C	5653.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #207	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5670.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #208	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	5653.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #209	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O	5698.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5659.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #210	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O	5664.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #211	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C	5694.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #212	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)C3O)C2O)=CC(O)=C1O	5676.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #213	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)C3O)C2O)=CC(O)=C1O	5674.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #214	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)C3O)C2O)=CC(O[Si](C)(C)C)=C1O	5660.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #215	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O[Si](C)(C)C	5644.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #216	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)C3O)C2O)=CC(O)=C1O	5685.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #217	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)C3O)C2O)=CC(O[Si](C)(C)C)=C1O	5615.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #218	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)C3O)C2O)=CC(O)=C1O[Si](C)(C)C	5596.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #219	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)C3O)C2O)=CC(O[Si](C)(C)C)=C1O	5656.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	5751.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #220	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)C3O)C2O)=CC(O)=C1O[Si](C)(C)C	5638.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #221	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5646.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #222	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O	5663.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #223	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O	5617.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #224	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C	5658.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #225	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)C3O)C2O)C=C1O	5641.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #226	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)C3O)C2O)C=C1O	5647.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #227	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)C3O)C2O)C=C1O	5648.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #228	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5736.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #229	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5721.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	5742.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #230	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5738.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #231	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5740.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	5747.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	5755.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	5731.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	5747.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5650.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5632.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5695.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	5698.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	5675.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	5680.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	5683.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	5653.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)C3O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	5683.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #36	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	5677.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #37	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	5651.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #38	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	5648.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #39	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	5648.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	5665.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #40	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	5613.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #41	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	5647.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #42	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	5720.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #43	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	5722.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #44	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	5733.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #45	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	5714.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #46	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C	5727.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #47	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C(O)C1O	5738.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #48	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C(O)C1O	5732.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #49	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O)C(O[Si](C)(C)C)C1O	5711.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)C(O)C2O)C(O)C(O)C1O	5731.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #50	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O[Si](C)(C)C	5726.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #51	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O	5738.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #52	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O	5716.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #53	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C	5730.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #54	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5724.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #55	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5713.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #56	C[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5721.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #57	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5772.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #58	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5790.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #59	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C2O)=CC(O)=C1O	5728.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O)C(O)C(O)C1O	5718.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #60	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C2O)C=C1O	5703.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #61	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5746.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #62	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	5736.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #63	C[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5751.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #64	C[Si](C)(C)OC1C(O)C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C1O	5739.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #65	C[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)OC(CO)C(O)C1O	5755.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #66	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5750.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #67	C[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	5743.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #68	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O[Si](C)(C)C)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5753.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #69	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5723.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C)C(O)C(O)C1O	5728.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #70	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5746.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #71	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)C1O)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5740.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #72	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)C3O)C2O)=CC(O)=C1O	5702.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #73	C[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)C1O)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5667.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #74	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5714.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #75	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5678.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #76	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5764.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #77	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	5757.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #78	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5770.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #79	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5747.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C)C(O)C1O	5740.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #80	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5768.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #81	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C(O)C(O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	5693.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #82	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)C3O)C2O)=CC(O)=C1O	5691.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #83	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)C3O)C2O)=CC(O)=C1O	5657.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #84	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C2O)=CC(O)=C1O	5687.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #85	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)C3O)C2O[Si](C)(C)C)=CC(O)=C1O	5707.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #86	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)C3O)C2O)=CC(O[Si](C)(C)C)=C1O	5664.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #87	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)C3O)C2O)=CC(O)=C1O[Si](C)(C)C	5649.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #88	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C(O)C(O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	5667.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #89	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)C3O)C2O)C=C1O	5658.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O[Si](C)(C)C)C1O	5721.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #90	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)C3O)C2O)C=C1O	5616.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #91	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C2O)C=C1O	5651.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #92	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)C3O)C2O[Si](C)(C)C)C=C1O	5684.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #93	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	5730.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #94	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5731.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #95	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5720.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #96	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5735.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #97	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O[Si](C)(C)C)C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O	5740.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #98	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O	5722.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],3TMS,isomer #99	C[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O[Si](C)(C)C)C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C	5740.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	6023.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)OC(CO)C(O)C1O	6086.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C1O	6091.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C1O	6098.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C(O)C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C1OC1OC(CO)C(O)C(O)C1O	6093.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C1O	6077.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	6087.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	6118.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6117.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O	6095.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)C=C1O	6132.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	6039.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO[Si](C)(C)C(C)(C)C)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	6161.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	6157.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	6165.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C1O[Si](C)(C)C(C)(C)C	6207.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6219.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	6225.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)C3O)C2O)=CC(O)=C1O	6176.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)C3O)C2O)C=C1O	6189.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	6194.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1OC1OC(CO)C(O)C(O)C1O	6175.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	6190.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	6184.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C(C)(C)C)C1O	6172.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C(C)(C)C)OC(CO)C(O)C1O	6179.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O[Si](C)(C)C(C)(C)C)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6207.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	6214.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O[Si](C)(C)C(C)(C)C)C2O)=CC(O)=C1O	6163.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O[Si](C)(C)C(C)(C)C)C2O)C=C1O	6179.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	6193.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1OC1OC(CO)C(O)C(O)C1O	6164.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	6184.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1C(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C1O	6164.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	6189.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C(C)(C)C)C2O)OC(CO)C(O)C1O	6175.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O	6185.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O[Si](C)(C)C(C)(C)C)C=C1O	6200.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C(C)(C)C)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	6227.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O[Si](C)(C)C(C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	6213.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	6182.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O	6194.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	6178.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	6188.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6213.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)C3O)C(O)C2O)C(O)C(O)C1O	6150.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	6208.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	6214.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	6200.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O	6230.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	6206.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2OC1OC(CO)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	6213.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	6197.0	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6224.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #48	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6200.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #49	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)C1O)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6205.8	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)C3O)C(O)C2O)C(O)C(O)C1O	6155.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #50	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O	6200.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #51	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(OC1OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C(O)C1O)C(O)C(C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O2	6206.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #52	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	6164.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #53	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O	6179.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #54	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)C3O)C2O)=CC(O)=C1O	6153.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #55	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)C3O)C2O)=CC(O)=C1O	6162.6	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #56	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O	6172.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #57	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O)C(O)C3O)C2O)=CC(O)=C1O[Si](C)(C)C(C)(C)C	6163.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #58	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O	6170.5	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #59	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)C3O)C2O)C=C1O	6188.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C(O)C1O	6168.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #60	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)C3O)C2O)C=C1O	6157.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #61	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(OC3OC(CO)C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)C3O)C2O)C=C1O	6163.2	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #62	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	6179.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #63	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	6162.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #64	CC(C)(C)[Si](C)(C)OCC1OC(OC2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C(O)C(O)C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	6167.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #65	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	6169.7	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #66	CC(C)(C)[Si](C)(C)OC1C(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	6189.1	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #67	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	6185.4	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C(O)C1O	6151.9	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O	6162.3	Semi standard non polar	33892256
Leucodelphinidin 3-[galactosyl-(1->4)-glucoside],2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2C(CO)OC(OC3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	6161.1	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 - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (Non-derivatized) - 70eV, Positive	splash10-00or-3534129000-6d6b8564c697bd67f30e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_11) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_1_12) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-17	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 - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 10V, Positive-QTOF	splash10-00fr-0209605000-8ac98b512c1be93cfb29	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 20V, Positive-QTOF	splash10-00di-0509400000-e4f544b0cd4f0de8dfba	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 40V, Positive-QTOF	splash10-00di-0906100000-a92ffbee4fa3b7f6fb98	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 10V, Negative-QTOF	splash10-0092-1427519000-64f3dacea57e38381c8b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 20V, Negative-QTOF	splash10-00di-1609402000-ef11d5c9b09e77826ff0	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 40V, Negative-QTOF	splash10-00fr-2906000000-fcc47fd4f00eb6ed0750	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 10V, Positive-QTOF	splash10-05fr-0109201000-c0c23fa902192a155032	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 20V, Positive-QTOF	splash10-006t-1903112000-9b571417aa01b28093c4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 40V, Positive-QTOF	splash10-007a-3904020000-138527489056cf49dad6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 10V, Negative-QTOF	splash10-0002-0001009000-a692318001a40d03f6ca	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 20V, Negative-QTOF	splash10-0ul1-1908854000-cef42ad169e2a10ba2fa	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] 40V, Negative-QTOF	splash10-0ufr-1946000000-a41bf405fc7fbd5f79f1	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	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

Not Available

FooDB ID

FDB010729

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131751298

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 Leucodelphinidin 3-[galactosyl-(1->4)-glucoside] (HMDB0032762)

MOL for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

3D MOL for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

3D SDF for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

3D-SDF for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

PDB for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

3D PDB for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

SMILES for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

INCHI for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

Structure for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

3D Structure for HMDB0032762 (Leucodelphinidin 3-[galactosyl-(1->4)-glucoside])

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra