Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:35:45 UTC

Update Date

2022-03-07 02:55:17 UTC

HMDB ID

HMDB0037355

Secondary Accession Numbers

HMDB37355

Metabolite Identification

Common Name

Quercetin 3-arabinoside 7-glucoside

Description

Quercetin 3-arabinoside 7-glucoside belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Quercetin 3-arabinoside 7-glucoside has been detected, but not quantified in, a few different foods, such as american pokeweeds (Phytolacca americana), fruits, and green vegetables. This could make quercetin 3-arabinoside 7-glucoside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Quercetin 3-arabinoside 7-glucoside.

Structure

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

  Mrv0541 05061309442D          

 42 46  0  0  0  0            999 V2000
    3.5724   -0.4125    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
    2.8579    0.8250    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
    0.0000    2.4750    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
    2.8579    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
    4.2868    0.8250    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
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    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
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    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
   -2.1434    2.0625    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
   -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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    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
    3.5724    2.0625    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
    2.8579   -4.9500    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    3.3000    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
   -2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    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
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  8  1  1  0  0  0  0
  8  3  2  0  0  0  0
  9  4  2  0  0  0  0
  9  5  1  0  0  0  0
 10  2  1  0  0  0  0
 11  3  1  0  0  0  0
 11 10  2  0  0  0  0
 12  4  1  0  0  0  0
 13  7  1  0  0  0  0
 14  5  2  0  0  0  0
 15  6  1  0  0  0  0
 16 12  2  0  0  0  0
 16 14  1  0  0  0  0
 17 13  1  0  0  0  0
 18 15  1  0  0  0  0
 19 16  1  0  0  0  0
 20 18  1  0  0  0  0
 21 17  1  0  0  0  0
 22 20  1  0  0  0  0
 23  8  1  0  0  0  0
 24 19  1  0  0  0  0
 24 23  2  0  0  0  0
 25 21  1  0  0  0  0
 26 22  1  0  0  0  0
 27  6  1  0  0  0  0
 28 10  1  0  0  0  0
 29 11  1  0  0  0  0
 30 12  1  0  0  0  0
 31 13  1  0  0  0  0
 32 17  1  0  0  0  0
 33 18  1  0  0  0  0
 34 19  2  0  0  0  0
 35 20  1  0  0  0  0
 36 21  1  0  0  0  0
 37 22  1  0  0  0  0
 38  7  1  0  0  0  0
 38 25  1  0  0  0  0
 39  9  1  0  0  0  0
 39 26  1  0  0  0  0
 40 14  1  0  0  0  0
 40 23  1  0  0  0  0
 41 15  1  0  0  0  0
 41 26  1  0  0  0  0
 42 24  1  0  0  0  0
 42 25  1  0  0  0  0
M  END

HMDB0037355
     RDKit          3D
Quercetin 3-arabinoside 7-glucoside
 70 74  0  0  0  0  0  0  0  0999 V2000
   -2.4175    1.7296   -2.4314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6306    1.0047   -1.8133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0182   -0.2765   -1.3790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3227   -0.6470   -1.6796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3409   -0.1723   -0.7812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8235   -1.2224   -0.0645 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7793   -0.9955    0.8710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7076    0.1007    0.4330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9431    0.0872    1.0469 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7844    0.0786   -1.0830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0415   -1.2274   -1.4695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4159    0.4507   -1.6545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3229    1.8247   -1.5429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1879   -1.0898   -0.7127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4663   -2.4528   -0.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5922   -3.0079    0.7173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7416   -4.2724    1.1786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7735   -5.0840    0.7493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9108   -6.3673    1.2297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6292   -4.5200   -0.1715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6801   -5.3059   -0.6277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4930   -3.2273   -0.6564 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0295   -0.6158   -0.4750 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4500    0.5616   -0.8474 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7435    0.9874   -0.5567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2356    2.2155   -0.9224 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5144    2.6475   -0.6403 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5123    1.9277    0.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863    2.6160    1.2313 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4880    1.8515    2.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6487    0.8011    2.8164 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5075    0.1092    3.6990 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6991    1.2328    1.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7842    1.4304    2.2971 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0087    1.9133    0.1335 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4935    3.2114    0.4013 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7943    1.9816   -0.7719 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8031    1.0078   -1.7568 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4334    3.0940   -1.6133 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1194    2.6949   -1.9238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6470    3.5703   -2.5997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3600    1.4463   -1.5439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9692    0.5805   -0.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2676   -0.6320    1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3451   -1.9147    1.1613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1755    1.0751    0.6679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8034   -0.0878    2.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5860    0.7205   -1.4238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3152   -1.7655   -0.6895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3018    0.1685   -2.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4893    2.2967   -2.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2309   -2.3992    1.0775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0132   -4.6366    1.9104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2458   -6.7190    1.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8600   -6.2395   -0.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1887   -2.8459   -1.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3418    0.2697   -0.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059    0.8929    0.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8139    2.5509    2.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8698    1.3456    3.4042 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2397    0.0930    2.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7534   -0.7463    3.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4951    0.1674    1.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5622    0.8486    2.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8100    1.3683   -0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7263    3.6435   -0.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8204    2.9858   -1.2755 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4207    1.2376   -2.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7792    4.0695   -1.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5301    3.5806   -2.9324 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
  3 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 14 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 30 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 26 39  2  0
 39 40  1  0
 40 41  1  0
 40 42  2  0
 42  2  1  0
 12  5  1  0
 22 15  1  0
 42 24  1  0
 37 28  1  0
  5 43  1  0
  7 44  1  0
  7 45  1  0
  8 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 12 50  1  0
 13 51  1  0
 16 52  1  0
 17 53  1  0
 19 54  1  0
 21 55  1  0
 22 56  1  0
 25 57  1  0
 28 58  1  0
 30 59  1  0
 31 60  1  0
 31 61  1  0
 32 62  1  0
 33 63  1  0
 34 64  1  0
 35 65  1  0
 36 66  1  0
 37 67  1  0
 38 68  1  0
 39 69  1  0
 41 70  1  0
M  END

  Mrv0541 05061309442D          

 42 46  0  0  0  0            999 V2000
    3.5724   -0.4125    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
    2.8579    0.8250    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
    0.0000    2.4750    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
    2.8579    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
    4.2868    0.8250    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
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    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
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    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
   -2.1434    2.0625    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
   -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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    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
    3.5724    2.0625    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
    2.8579   -4.9500    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    3.3000    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
   -2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    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
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  8  1  1  0  0  0  0
  8  3  2  0  0  0  0
  9  4  2  0  0  0  0
  9  5  1  0  0  0  0
 10  2  1  0  0  0  0
 11  3  1  0  0  0  0
 11 10  2  0  0  0  0
 12  4  1  0  0  0  0
 13  7  1  0  0  0  0
 14  5  2  0  0  0  0
 15  6  1  0  0  0  0
 16 12  2  0  0  0  0
 16 14  1  0  0  0  0
 17 13  1  0  0  0  0
 18 15  1  0  0  0  0
 19 16  1  0  0  0  0
 20 18  1  0  0  0  0
 21 17  1  0  0  0  0
 22 20  1  0  0  0  0
 23  8  1  0  0  0  0
 24 19  1  0  0  0  0
 24 23  2  0  0  0  0
 25 21  1  0  0  0  0
 26 22  1  0  0  0  0
 27  6  1  0  0  0  0
 28 10  1  0  0  0  0
 29 11  1  0  0  0  0
 30 12  1  0  0  0  0
 31 13  1  0  0  0  0
 32 17  1  0  0  0  0
 33 18  1  0  0  0  0
 34 19  2  0  0  0  0
 35 20  1  0  0  0  0
 36 21  1  0  0  0  0
 37 22  1  0  0  0  0
 38  7  1  0  0  0  0
 38 25  1  0  0  0  0
 39  9  1  0  0  0  0
 39 26  1  0  0  0  0
 40 14  1  0  0  0  0
 40 23  1  0  0  0  0
 41 15  1  0  0  0  0
 41 26  1  0  0  0  0
 42 24  1  0  0  0  0
 42 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037355

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C26H28O16/c27-6-15-18(33)20(35)22(37)26(41-15)39-9-4-12(30)16-14(5-9)40-23(8-1-2-10(28)11(29)3-8)24(19(16)34)42-25-21(36)17(32)13(31)7-38-25/h1-5,13,15,17-18,20-22,25-33,35-37H,6-7H2

> <INCHI_KEY>
QOTHERNBBVJOEC-UHFFFAOYSA-N

> <FORMULA>
C26H28O16

> <MOLECULAR_WEIGHT>
596.4909

> <EXACT_MASS>
596.137734848

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_AVERAGE_POLARIZABILITY>
56.025147149333876

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]-4H-chromen-4-one

> <ALOGPS_LOGP>
-0.58

> <JCHEM_LOGP>
-1.782568447333333

> <ALOGPS_LOGS>
-2.24

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.746788373551103

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.107097109391521

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6483953457595923

> <JCHEM_POLAR_SURFACE_AREA>
265.52

> <JCHEM_REFRACTIVITY>
135.45739999999992

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.46e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037355
     RDKit          3D
Quercetin 3-arabinoside 7-glucoside
 70 74  0  0  0  0  0  0  0  0999 V2000
   -2.4175    1.7296   -2.4314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6306    1.0047   -1.8133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0182   -0.2765   -1.3790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3227   -0.6470   -1.6796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3409   -0.1723   -0.7812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8235   -1.2224   -0.0645 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7793   -0.9955    0.8710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7076    0.1007    0.4330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9431    0.0872    1.0469 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7844    0.0786   -1.0830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0415   -1.2274   -1.4695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4159    0.4507   -1.6545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3229    1.8247   -1.5429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1879   -1.0898   -0.7127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4663   -2.4528   -0.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5922   -3.0079    0.7173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7416   -4.2724    1.1786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7735   -5.0840    0.7493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9108   -6.3673    1.2297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6292   -4.5200   -0.1715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6801   -5.3059   -0.6277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4930   -3.2273   -0.6564 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0295   -0.6158   -0.4750 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4500    0.5616   -0.8474 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7435    0.9874   -0.5567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2356    2.2155   -0.9224 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5144    2.6475   -0.6403 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5123    1.9277    0.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863    2.6160    1.2313 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4880    1.8515    2.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6487    0.8011    2.8164 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5075    0.1092    3.6990 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6991    1.2328    1.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7842    1.4304    2.2971 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0087    1.9133    0.1335 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4935    3.2114    0.4013 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7943    1.9816   -0.7719 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8031    1.0078   -1.7568 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4334    3.0940   -1.6133 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1194    2.6949   -1.9238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6470    3.5703   -2.5997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3600    1.4463   -1.5439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9692    0.5805   -0.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2676   -0.6320    1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3451   -1.9147    1.1613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1755    1.0751    0.6679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8034   -0.0878    2.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5860    0.7205   -1.4238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3152   -1.7655   -0.6895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3018    0.1685   -2.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4893    2.2967   -2.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2309   -2.3992    1.0775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0132   -4.6366    1.9104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2458   -6.7190    1.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8600   -6.2395   -0.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1887   -2.8459   -1.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3418    0.2697   -0.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059    0.8929    0.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8139    2.5509    2.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8698    1.3456    3.4042 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2397    0.0930    2.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7534   -0.7463    3.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4951    0.1674    1.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5622    0.8486    2.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8100    1.3683   -0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7263    3.6435   -0.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8204    2.9858   -1.2755 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4207    1.2376   -2.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7792    4.0695   -1.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5301    3.5806   -2.9324 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
  3 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 14 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 30 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 26 39  2  0
 39 40  1  0
 40 41  1  0
 40 42  2  0
 42  2  1  0
 12  5  1  0
 22 15  1  0
 42 24  1  0
 37 28  1  0
  5 43  1  0
  7 44  1  0
  7 45  1  0
  8 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 12 50  1  0
 13 51  1  0
 16 52  1  0
 17 53  1  0
 19 54  1  0
 21 55  1  0
 22 56  1  0
 25 57  1  0
 28 58  1  0
 30 59  1  0
 31 60  1  0
 31 61  1  0
 32 62  1  0
 33 63  1  0
 34 64  1  0
 35 65  1  0
 36 66  1  0
 37 67  1  0
 38 68  1  0
 39 69  1  0
 41 70  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       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668  -5.390   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       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.000   6.160   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -2.667   6.160   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -5.335   4.620   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      -5.335   1.540   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2    8                                                       
CONECT    2    1   10                                                       
CONECT    3    8   11                                                       
CONECT    4    9   12                                                       
CONECT    5    9   14                                                       
CONECT    6   15   27                                                       
CONECT    7   13   38                                                       
CONECT    8    1    3   23                                                  
CONECT    9    4    5   39                                                  
CONECT   10    2   11   28                                                  
CONECT   11    3   10   29                                                  
CONECT   12    4   16   30                                                  
CONECT   13    7   17   31                                                  
CONECT   14    5   16   40                                                  
CONECT   15    6   18   41                                                  
CONECT   16   12   14   19                                                  
CONECT   17   13   21   32                                                  
CONECT   18   15   20   33                                                  
CONECT   19   16   24   34                                                  
CONECT   20   18   22   35                                                  
CONECT   21   17   25   36                                                  
CONECT   22   20   26   37                                                  
CONECT   23    8   24   40                                                  
CONECT   24   19   23   42                                                  
CONECT   25   21   38   42                                                  
CONECT   26   22   39   41                                                  
CONECT   27    6                                                            
CONECT   28   10                                                            
CONECT   29   11                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   17                                                            
CONECT   33   18                                                            
CONECT   34   19                                                            
CONECT   35   20                                                            
CONECT   36   21                                                            
CONECT   37   22                                                            
CONECT   38    7   25                                                       
CONECT   39    9   26                                                       
CONECT   40   14   23                                                       
CONECT   41   15   26                                                       
CONECT   42   24   25                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

COMPND    HMDB0037355
HETATM    1  O1  UNL     1      -2.417   1.730  -2.431  1.00  0.00           O  
HETATM    2  C1  UNL     1      -1.631   1.005  -1.813  1.00  0.00           C  
HETATM    3  C2  UNL     1      -2.018  -0.277  -1.379  1.00  0.00           C  
HETATM    4  O2  UNL     1      -3.323  -0.647  -1.680  1.00  0.00           O  
HETATM    5  C3  UNL     1      -4.341  -0.172  -0.781  1.00  0.00           C  
HETATM    6  O3  UNL     1      -4.823  -1.222  -0.065  1.00  0.00           O  
HETATM    7  C4  UNL     1      -5.779  -0.996   0.871  1.00  0.00           C  
HETATM    8  C5  UNL     1      -6.708   0.101   0.433  1.00  0.00           C  
HETATM    9  O4  UNL     1      -7.943   0.087   1.047  1.00  0.00           O  
HETATM   10  C6  UNL     1      -6.784   0.079  -1.083  1.00  0.00           C  
HETATM   11  O5  UNL     1      -7.041  -1.227  -1.470  1.00  0.00           O  
HETATM   12  C7  UNL     1      -5.416   0.451  -1.654  1.00  0.00           C  
HETATM   13  O6  UNL     1      -5.323   1.825  -1.543  1.00  0.00           O  
HETATM   14  C8  UNL     1      -1.188  -1.090  -0.713  1.00  0.00           C  
HETATM   15  C9  UNL     1      -1.466  -2.453  -0.213  1.00  0.00           C  
HETATM   16  C10 UNL     1      -0.592  -3.008   0.717  1.00  0.00           C  
HETATM   17  C11 UNL     1      -0.742  -4.272   1.179  1.00  0.00           C  
HETATM   18  C12 UNL     1      -1.773  -5.084   0.749  1.00  0.00           C  
HETATM   19  O7  UNL     1      -1.911  -6.367   1.230  1.00  0.00           O  
HETATM   20  C13 UNL     1      -2.629  -4.520  -0.172  1.00  0.00           C  
HETATM   21  O8  UNL     1      -3.680  -5.306  -0.628  1.00  0.00           O  
HETATM   22  C14 UNL     1      -2.493  -3.227  -0.656  1.00  0.00           C  
HETATM   23  O9  UNL     1       0.029  -0.616  -0.475  1.00  0.00           O  
HETATM   24  C15 UNL     1       0.450   0.562  -0.847  1.00  0.00           C  
HETATM   25  C16 UNL     1       1.743   0.987  -0.557  1.00  0.00           C  
HETATM   26  C17 UNL     1       2.236   2.216  -0.922  1.00  0.00           C  
HETATM   27  O10 UNL     1       3.514   2.647  -0.640  1.00  0.00           O  
HETATM   28  C18 UNL     1       4.512   1.928   0.032  1.00  0.00           C  
HETATM   29  O11 UNL     1       4.786   2.616   1.231  1.00  0.00           O  
HETATM   30  C19 UNL     1       5.488   1.852   2.129  1.00  0.00           C  
HETATM   31  C20 UNL     1       4.649   0.801   2.816  1.00  0.00           C  
HETATM   32  O12 UNL     1       5.507   0.109   3.699  1.00  0.00           O  
HETATM   33  C21 UNL     1       6.699   1.233   1.451  1.00  0.00           C  
HETATM   34  O13 UNL     1       7.784   1.430   2.297  1.00  0.00           O  
HETATM   35  C22 UNL     1       7.009   1.913   0.133  1.00  0.00           C  
HETATM   36  O14 UNL     1       7.493   3.211   0.401  1.00  0.00           O  
HETATM   37  C23 UNL     1       5.794   1.982  -0.772  1.00  0.00           C  
HETATM   38  O15 UNL     1       5.803   1.008  -1.757  1.00  0.00           O  
HETATM   39  C24 UNL     1       1.433   3.094  -1.613  1.00  0.00           C  
HETATM   40  C25 UNL     1       0.119   2.695  -1.924  1.00  0.00           C  
HETATM   41  O16 UNL     1      -0.647   3.570  -2.600  1.00  0.00           O  
HETATM   42  C26 UNL     1      -0.360   1.446  -1.544  1.00  0.00           C  
HETATM   43  H1  UNL     1      -3.969   0.581  -0.077  1.00  0.00           H  
HETATM   44  H2  UNL     1      -5.268  -0.632   1.793  1.00  0.00           H  
HETATM   45  H3  UNL     1      -6.345  -1.915   1.161  1.00  0.00           H  
HETATM   46  H4  UNL     1      -6.175   1.075   0.668  1.00  0.00           H  
HETATM   47  H5  UNL     1      -7.803  -0.088   2.001  1.00  0.00           H  
HETATM   48  H6  UNL     1      -7.586   0.721  -1.424  1.00  0.00           H  
HETATM   49  H7  UNL     1      -7.315  -1.765  -0.690  1.00  0.00           H  
HETATM   50  H8  UNL     1      -5.302   0.168  -2.703  1.00  0.00           H  
HETATM   51  H9  UNL     1      -5.489   2.297  -2.405  1.00  0.00           H  
HETATM   52  H10 UNL     1       0.231  -2.399   1.078  1.00  0.00           H  
HETATM   53  H11 UNL     1      -0.013  -4.637   1.910  1.00  0.00           H  
HETATM   54  H12 UNL     1      -1.246  -6.719   1.905  1.00  0.00           H  
HETATM   55  H13 UNL     1      -3.860  -6.239  -0.345  1.00  0.00           H  
HETATM   56  H14 UNL     1      -3.189  -2.846  -1.400  1.00  0.00           H  
HETATM   57  H15 UNL     1       2.342   0.270  -0.014  1.00  0.00           H  
HETATM   58  H16 UNL     1       4.206   0.893   0.246  1.00  0.00           H  
HETATM   59  H17 UNL     1       5.814   2.551   2.951  1.00  0.00           H  
HETATM   60  H18 UNL     1       3.870   1.346   3.404  1.00  0.00           H  
HETATM   61  H19 UNL     1       4.240   0.093   2.099  1.00  0.00           H  
HETATM   62  H20 UNL     1       5.753  -0.746   3.283  1.00  0.00           H  
HETATM   63  H21 UNL     1       6.495   0.167   1.270  1.00  0.00           H  
HETATM   64  H22 UNL     1       8.562   0.849   2.023  1.00  0.00           H  
HETATM   65  H23 UNL     1       7.810   1.368  -0.365  1.00  0.00           H  
HETATM   66  H24 UNL     1       7.726   3.644  -0.472  1.00  0.00           H  
HETATM   67  H25 UNL     1       5.820   2.986  -1.275  1.00  0.00           H  
HETATM   68  H26 UNL     1       6.421   1.238  -2.475  1.00  0.00           H  
HETATM   69  H27 UNL     1       1.779   4.070  -1.921  1.00  0.00           H  
HETATM   70  H28 UNL     1      -1.530   3.581  -2.932  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   42
CONECT    3    4   14   14
CONECT    4    5
CONECT    5    6   12   43
CONECT    6    7
CONECT    7    8   44   45
CONECT    8    9   10   46
CONECT    9   47
CONECT   10   11   12   48
CONECT   11   49
CONECT   12   13   50
CONECT   13   51
CONECT   14   15   23
CONECT   15   16   16   22
CONECT   16   17   52
CONECT   17   18   18   53
CONECT   18   19   20
CONECT   19   54
CONECT   20   21   22   22
CONECT   21   55
CONECT   22   56
CONECT   23   24
CONECT   24   25   25   42
CONECT   25   26   57
CONECT   26   27   39   39
CONECT   27   28
CONECT   28   29   37   58
CONECT   29   30
CONECT   30   31   33   59
CONECT   31   32   60   61
CONECT   32   62
CONECT   33   34   35   63
CONECT   34   64
CONECT   35   36   37   65
CONECT   36   66
CONECT   37   38   67
CONECT   38   68
CONECT   39   40   69
CONECT   40   41   42   42
CONECT   41   70
END

HMDB0037355
     RDKit          3D
Quercetin 3-arabinoside 7-glucoside
 70 74  0  0  0  0  0  0  0  0999 V2000
   -2.4175    1.7296   -2.4314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6306    1.0047   -1.8133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0182   -0.2765   -1.3790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3227   -0.6470   -1.6796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3409   -0.1723   -0.7812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8235   -1.2224   -0.0645 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7793   -0.9955    0.8710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7076    0.1007    0.4330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9431    0.0872    1.0469 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7844    0.0786   -1.0830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0415   -1.2274   -1.4695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4159    0.4507   -1.6545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3229    1.8247   -1.5429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1879   -1.0898   -0.7127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4663   -2.4528   -0.2132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5922   -3.0079    0.7173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7416   -4.2724    1.1786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7735   -5.0840    0.7493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9108   -6.3673    1.2297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6292   -4.5200   -0.1715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6801   -5.3059   -0.6277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4930   -3.2273   -0.6564 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0295   -0.6158   -0.4750 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4500    0.5616   -0.8474 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7435    0.9874   -0.5567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2356    2.2155   -0.9224 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5144    2.6475   -0.6403 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5123    1.9277    0.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863    2.6160    1.2313 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4880    1.8515    2.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6487    0.8011    2.8164 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5075    0.1092    3.6990 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6991    1.2328    1.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7842    1.4304    2.2971 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0087    1.9133    0.1335 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4935    3.2114    0.4013 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7943    1.9816   -0.7719 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8031    1.0078   -1.7568 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4334    3.0940   -1.6133 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1194    2.6949   -1.9238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6470    3.5703   -2.5997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3600    1.4463   -1.5439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9692    0.5805   -0.0773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2676   -0.6320    1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3451   -1.9147    1.1613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1755    1.0751    0.6679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8034   -0.0878    2.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5860    0.7205   -1.4238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3152   -1.7655   -0.6895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3018    0.1685   -2.7029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4893    2.2967   -2.4049 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2309   -2.3992    1.0775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0132   -4.6366    1.9104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2458   -6.7190    1.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8600   -6.2395   -0.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1887   -2.8459   -1.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3418    0.2697   -0.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059    0.8929    0.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8139    2.5509    2.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8698    1.3456    3.4042 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2397    0.0930    2.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7534   -0.7463    3.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4951    0.1674    1.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5622    0.8486    2.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8100    1.3683   -0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7263    3.6435   -0.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8204    2.9858   -1.2755 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4207    1.2376   -2.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7792    4.0695   -1.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5301    3.5806   -2.9324 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
  3 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  2  0
 14 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 30 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 26 39  2  0
 39 40  1  0
 40 41  1  0
 40 42  2  0
 42  2  1  0
 12  5  1  0
 22 15  1  0
 42 24  1  0
 37 28  1  0
  5 43  1  0
  7 44  1  0
  7 45  1  0
  8 46  1  0
  9 47  1  0
 10 48  1  0
 11 49  1  0
 12 50  1  0
 13 51  1  0
 16 52  1  0
 17 53  1  0
 19 54  1  0
 21 55  1  0
 22 56  1  0
 25 57  1  0
 28 58  1  0
 30 59  1  0
 31 60  1  0
 31 61  1  0
 32 62  1  0
 33 63  1  0
 34 64  1  0
 35 65  1  0
 36 66  1  0
 37 67  1  0
 38 68  1  0
 39 69  1  0
 41 70  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Quercetin 3-alpha-L-arabionopyranoside-7-glucoside	HMDB

Chemical Formula

C₂₆H₂₈O₁₆

Average Molecular Weight

596.4909

Monoisotopic Molecular Weight

596.137734848

IUPAC Name

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]-4H-chromen-4-one

Traditional Name

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]chromen-4-one

CAS Registry Number

28452-84-8

SMILES

OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C26H28O16/c27-6-15-18(33)20(35)22(37)26(41-15)39-9-4-12(30)16-14(5-9)40-23(8-1-2-10(28)11(29)3-8)24(19(16)34)42-25-21(36)17(32)13(31)7-38-25/h1-5,13,15,17-18,20-22,25-33,35-37H,6-7H2

InChI Key

QOTHERNBBVJOEC-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

Flavonoid-3-o-glycoside
Flavonoid-7-o-glycoside
Hydroxyflavonoid
Flavone
3'-hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
Phenolic glycoside
O-glycosyl compound
Glycosyl compound
Chromone
Benzopyran
1-benzopyran
Catechol
1-hydroxy-2-unsubstituted benzenoid
Pyranone
1-hydroxy-4-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Pyran
Monosaccharide
Benzenoid
Oxane
Heteroaromatic compound
Vinylogous acid
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Polyol
Primary alcohol
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organooxygen 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: HMDB0037355)
Cytoplasm (HMDB: HMDB0037355)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037355)

Source

Exogenous

Exogenous (HMDB: HMDB0037355)

Food

Food (HMDB: HMDB0037355)

Vegetable

Shoot vegetable

American pokeweed (FooDB: FOOD00437)

Leaf vegetable

Green vegetables (FooDB: FOOD00872)

Fruit

Fruits (FooDB: FOOD00871)

Endogenous

Plant

Plant (HMDB: HMDB0037355)

Process

Not Available

Role

Biological role

Nutrient (HMDB: HMDB0037355)

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	3.46 g/L	ALOGPS
logP	-0.58	ALOGPS
logP	-1.8	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	8.11	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	265.52 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	135.46 m³·mol⁻¹	ChemAxon
Polarizability	56.03 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]+	232.869	31661259
DarkChem	[M-H]-	229.444	31661259
DeepCCS	[M+H]+	223.137	30932474
DeepCCS	[M-H]-	221.09	30932474
DeepCCS	[M-2H]-	254.329	30932474
DeepCCS	[M+Na]+	228.972	30932474
AllCCS	[M+H]+	228.4	32859911
AllCCS	[M+H-H2O]+	227.1	32859911
AllCCS	[M+NH4]+	229.6	32859911
AllCCS	[M+Na]+	230.0	32859911
AllCCS	[M-H]-	224.2	32859911
AllCCS	[M+Na-2H]-	226.2	32859911
AllCCS	[M+HCOO]-	228.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Quercetin 3-arabinoside 7-glucoside	OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O	5081.6	Standard polar	33892256
Quercetin 3-arabinoside 7-glucoside	OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O	5215.3	Standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside	OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(OC3=C2)C2=CC(O)=C(O)C=C2)C(O)C(O)C1O	5570.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5460.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #10	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O	5496.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #2	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5497.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #3	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C(O)C1O	5517.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #4	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C1O	5488.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #5	C[Si](C)(C)OC1C(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)OCC(O)C1O	5508.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #6	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5537.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #7	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5549.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #8	C[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)OC(CO)C(O)C1O	5504.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TMS,isomer #9	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C1O	5496.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5382.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #10	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5387.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #11	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5371.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #12	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5401.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #13	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5383.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #14	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5365.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #15	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5403.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #16	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5365.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #17	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5395.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #18	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5418.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #19	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5404.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5390.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #20	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O)=C3C2=O)C(O)C1O	5402.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #21	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C(O)C1O	5395.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #22	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O)C1O	5415.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #23	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O	5423.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #24	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C(O)C1O[Si](C)(C)C	5418.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #25	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5368.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #26	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5350.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #27	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O)=C3C2=O)C1O	5377.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #28	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C1O	5364.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #29	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C1O	5392.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5367.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #30	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C1O[Si](C)(C)C	5415.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #31	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5409.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #32	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5393.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #33	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O	5397.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #34	C[Si](C)(C)OC1C(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)OCC(O)C1O	5390.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #35	C[Si](C)(C)OC1C(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)OCC(O)C1O	5415.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #36	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5380.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #37	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5354.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #38	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5395.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #39	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5388.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5387.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #40	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5394.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #41	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5373.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #42	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5411.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #43	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C1O	5404.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #44	C[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)OC(CO)C(O)C1O[Si](C)(C)C	5422.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #45	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O[Si](C)(C)C	5405.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5390.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5376.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5405.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5386.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5384.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5249.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5280.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #100	C[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)OC(CO)C(O)C1O	5272.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #101	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5253.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #102	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5220.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #103	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5272.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #104	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5265.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #105	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5230.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #106	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5193.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #107	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5250.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #108	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C1O	5269.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #109	C[Si](C)(C)OC1C(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)OCC(O)C1O	5262.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5246.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #110	C[Si](C)(C)OC1C(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O)=C3C2=O)OCC(O)C1O	5298.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #111	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5209.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #112	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5229.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #113	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5255.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #114	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5247.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #115	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5222.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #116	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5278.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #117	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5233.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #118	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5251.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #119	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5269.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5223.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #120	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5313.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5297.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5263.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5275.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5251.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5192.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5166.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5253.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5203.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5221.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5234.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5240.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5218.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5284.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5251.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5263.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5237.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5267.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5214.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5237.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5242.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5247.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5190.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5218.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5287.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5307.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #36	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5272.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #37	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5252.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #38	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5264.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #39	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5224.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5204.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #40	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5195.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #41	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5267.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #42	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5215.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #43	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5257.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #44	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5277.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #45	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5175.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #46	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5146.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #47	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5235.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #48	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5180.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #49	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5225.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5180.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #50	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5239.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #51	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5214.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #52	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5278.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #53	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5227.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #54	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5269.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #55	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5239.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #56	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5175.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #57	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5229.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #58	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5239.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #59	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5214.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5267.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #60	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5144.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #61	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5202.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #62	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5263.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #63	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5277.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #64	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5251.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #65	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5256.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #66	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5224.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #67	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5275.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #68	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5244.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #69	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5264.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5227.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #70	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5273.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #71	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5238.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #72	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5199.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #73	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5255.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #74	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5223.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #75	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5246.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #76	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C(O)C1O	5270.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #77	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O)C1O	5282.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #78	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O	5295.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #79	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O)=C3C2=O)C(O)C1O[Si](C)(C)C	5276.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5245.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #80	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O)C1O	5304.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #81	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O	5273.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #82	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C(O)C1O[Si](C)(C)C	5254.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #83	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O	5304.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #84	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O)C1O[Si](C)(C)C	5285.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #85	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5352.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #86	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5208.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #87	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5170.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #88	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5223.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #89	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5235.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5265.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #90	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5215.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #91	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5181.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #92	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5141.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #93	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5194.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #94	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5214.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #95	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C1O	5230.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #96	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C1O	5241.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #97	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O	5261.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #98	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C1O	5264.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,3TMS,isomer #99	C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C1O	5242.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5092.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	4953.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #100	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5040.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #101	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	4980.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #102	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5040.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #103	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5099.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #104	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5126.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #105	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5100.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #106	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5061.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #107	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5039.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #108	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5126.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #109	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5076.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #11	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5089.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #110	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5127.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #111	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	4999.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #112	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	4943.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #113	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5004.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #114	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5015.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #115	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	4975.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #116	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	4920.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #117	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	4979.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #118	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5057.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #119	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5090.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #12	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5028.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #120	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5066.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #121	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5071.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #122	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5002.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #123	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5078.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #124	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5091.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #125	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5045.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #126	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	4976.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #127	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5054.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #128	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5117.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #129	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5143.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #13	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5066.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #130	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5115.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #131	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5043.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #132	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5067.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #133	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5082.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #134	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5047.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #135	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5015.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #136	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5080.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #137	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5022.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #138	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5047.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #139	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5027.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #14	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5043.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #140	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5155.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #141	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5080.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #142	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5096.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #143	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5072.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #144	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5106.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #145	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5112.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #146	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5097.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #147	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5029.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #148	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5062.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #149	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5066.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #15	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5020.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #150	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5087.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #151	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5122.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #152	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5135.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #153	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5130.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #154	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5091.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #155	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5117.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #156	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5064.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #157	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5079.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #158	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5053.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #159	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5090.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #16	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5128.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #160	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5081.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #161	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5010.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #162	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5044.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #163	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5070.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #164	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5108.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #165	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5117.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #166	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O)C1O	5168.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #167	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O	5164.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #168	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C(O)C1O[Si](C)(C)C	5124.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #169	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O	5177.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #17	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5085.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #170	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O)C1O[Si](C)(C)C	5142.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #171	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5187.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #172	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O	5181.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #173	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O)C1O[Si](C)(C)C	5143.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #174	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5161.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #175	C[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5195.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #176	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5024.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #177	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5039.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #178	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5075.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #179	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5053.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #18	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5109.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #180	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5044.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #181	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5035.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #182	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5001.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #183	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5091.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #184	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5073.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #185	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5094.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #186	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5005.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #187	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5018.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #188	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5058.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #189	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5023.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #19	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5049.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #190	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5017.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #191	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5075.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #192	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C1O	5127.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #193	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=CC(O)=C3C2=O)C1O[Si](C)(C)C	5125.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #194	C[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C1O	5140.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #195	C[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O)=C3C2=O)C1O[Si](C)(C)C	5143.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #196	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5085.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #197	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5101.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #198	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5114.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #199	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5106.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5112.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #20	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5075.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #200	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5073.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #201	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5137.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #202	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5068.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #203	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5083.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #204	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5089.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #205	C[Si](C)(C)OC1C(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=CC(O)=C3C2=O)OCC(O)C1O	5169.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #206	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5099.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #207	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O[Si](C)(C)C	5091.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #208	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5109.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #209	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O[Si](C)(C)C	5115.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #21	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5007.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #210	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C=C3O2)C=C1O	5114.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #22	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5052.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #23	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5051.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #24	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4982.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #25	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5028.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #26	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5133.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #27	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5149.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #28	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5114.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #29	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5171.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5047.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #30	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5066.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #31	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5047.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #32	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5159.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #33	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5116.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #34	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5143.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #35	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5095.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #36	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5077.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #37	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5185.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #38	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5149.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #39	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5167.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5021.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #40	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5090.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #41	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5122.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #42	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5058.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #43	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5097.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #44	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5105.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #45	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5038.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #46	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5077.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #47	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5174.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #48	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5193.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #49	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5162.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5138.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #50	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5065.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #51	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5045.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #52	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5155.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #53	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5112.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #54	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5139.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #55	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5028.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #56	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5060.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #57	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4998.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #58	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5038.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #59	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5037.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5086.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #60	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	4970.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #61	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5013.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #62	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5129.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #63	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5154.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #64	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5115.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #65	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5088.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #66	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5122.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #67	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5062.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #68	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5099.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #69	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5106.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O[Si](C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5117.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #70	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5043.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #71	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5081.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #72	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5167.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #73	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5186.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #74	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5153.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #75	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O	5118.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #76	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O	5057.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #77	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C	5093.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #78	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5104.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #79	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5126.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5085.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #80	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5087.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #81	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5088.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #82	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5111.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #83	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5072.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #84	C[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5213.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #85	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5142.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #86	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)C=C1O	5040.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #87	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C=C3O2)=CC=C1O	5020.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #88	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5108.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #89	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5054.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C)C4O)=C(C4=CC=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	4981.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #90	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5110.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #91	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)C=C1O	5058.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #92	C[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C=C3O2)=CC=C1O	5037.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #93	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5122.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #94	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5070.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #95	C[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5122.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #96	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5064.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #97	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5003.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #98	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O	5064.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,4TMS,isomer #99	C[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C)C=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C	5078.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5673.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O	5739.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5686.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C(O)C1O	5751.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C1O	5729.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)OCC(O)C1O	5745.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5717.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5734.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)OC(CO)C(O)C1O	5746.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C1O	5741.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O[Si](C)(C)C(C)(C)C)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5753.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5766.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5753.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5768.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5778.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5750.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O[Si](C)(C)C(C)(C)C)C(O)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5788.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O[Si](C)(C)C(C)(C)C)C1O)=C(C1=CC=C(O)C(O)=C1)O2	5754.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC(OC2OC(CO)C(O)C(O)C2O)=CC2=C1C(=O)C(OC1OCC(O)C(O)C1O[Si](C)(C)C(C)(C)C)=C(C1=CC=C(O)C(O)=C1)O2	5766.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5800.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC(C2=C(OC3OCC(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5774.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O[Si](C)(C)C(C)(C)C)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5780.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)=CC(O)=C3C2=O)C(O)C1O	5795.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)=CC(O)=C3C2=O)C(O)C1O	5780.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(O)C1O	5799.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C(O[Si](C)(C)C(C)(C)C)C1O	5811.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C(O)C1O[Si](C)(C)C(C)(C)C	5794.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5765.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5734.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)=CC(O)=C3C2=O)C1O	5756.4	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)=CC(O)=C3C2=O)C1O	5742.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C1O	5759.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O[Si](C)(C)C(C)(C)C)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5745.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1C(O)COC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O)=CC(O)=C3C2=O)C1O[Si](C)(C)C(C)(C)C	5786.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O	5775.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)=CC=C1O	5747.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O	5772.7	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1C(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)=CC(O)=C3C2=O)OCC(O)C1O	5756.2	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1C(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)OCC(O)C1O	5779.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)=CC=C1O	5744.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)=CC=C1O	5732.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1=CC(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)=CC=C1O	5748.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C	5762.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O[Si](C)(C)C(C)(C)C)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O	5761.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C=C3O2)C=C1O	5773.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C=C3O2)C=C1O	5764.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(OC3OCC(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C=C3O2)C=C1O	5776.0	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C1O	5785.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1C(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	5792.6	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C1O[Si](C)(C)C(C)(C)C	5774.9	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)C(O)C(O)C1O	5765.1	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)C(O)C(O)C1O	5735.8	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	5778.3	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	5769.5	Semi standard non polar	33892256
Quercetin 3-arabinoside 7-glucoside,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC(O)=C3C(=O)C(OC4OCC(O)C(O)C4O)=C(C4=CC=C(O)C(O)=C4)OC3=C2)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	5752.5	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (Non-derivatized) - 70eV, Positive	splash10-0fc0-3500190000-dfe3c81bb3eb5a342d15	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (1 TMS) - 70eV, Positive	splash10-0udi-5610119000-4e5e760a6856060eacf5	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS ("Quercetin 3-arabinoside 7-glucoside,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-arabinoside 7-glucoside GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 10V, Positive-QTOF	splash10-0171-0101940000-c1a71e0b3f732342db1d	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 20V, Positive-QTOF	splash10-0udi-0219800000-425f0b517d96683efbaf	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 40V, Positive-QTOF	splash10-0udi-1439200000-f63460bff2c3a9a17716	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 10V, Negative-QTOF	splash10-0002-2401980000-3757f629d67d833404e9	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 20V, Negative-QTOF	splash10-001j-1421920000-2a243963be40f36e6cc1	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 40V, Negative-QTOF	splash10-0005-9687200000-fe38e4fc1a66474282fb	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 10V, Positive-QTOF	splash10-000j-0000940000-ee30458dac8e7ff4e2d1	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 20V, Positive-QTOF	splash10-000i-0000910000-d38871863d8eb16c1b5f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 40V, Positive-QTOF	splash10-000i-0000900000-1453f61e7eeaeb92b36b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 10V, Negative-QTOF	splash10-0002-0000090000-9ad7e32f889f9d109db5	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 20V, Negative-QTOF	splash10-000t-0000590000-d318948dba784fbee87a	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 7-glucoside 40V, Negative-QTOF	splash10-001i-0000910000-d4ddcfa995aea8929f0e	2021-09-25	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

FDB016379

KNApSAcK ID

C00005420

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

14054266

PDB ID

Not Available

ChEBI ID

176246

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 Quercetin 3-arabinoside 7-glucoside (HMDB0037355)

MOL for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

3D MOL for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

3D SDF for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

3D-SDF for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

PDB for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

3D PDB for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

SMILES for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

INCHI for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

Structure for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

3D Structure for HMDB0037355 (Quercetin 3-arabinoside 7-glucoside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra