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

2012-09-12 02:02:03 UTC

Update Date

2022-03-07 02:56:36 UTC

HMDB ID

HMDB0040486

Secondary Accession Numbers

HMDB40486

Metabolite Identification

Common Name

Quercetin 3-(2-glucosylrhamnoside)

Description

Quercetin 3-(2-glucosylrhamnoside) belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. Quercetin 3-(2-glucosylrhamnoside) has been detected, but not quantified in, fats and oils and ginkgo nuts (Ginkgo biloba). This could make quercetin 3-(2-glucosylrhamnoside) a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Quercetin 3-(2-glucosylrhamnoside).

Structure

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


  Mrv0541 05061311522D          

 43 47  0  0  0  0            999 V2000
    1.4289   -4.1250    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
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    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
    4.2868    0.0000    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    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
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    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
    5.7158   -2.4750    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
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    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
    6.4302   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    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
    7.1447   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    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
    5.0013   -3.7125    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
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  8  1  1  0  0  0  0
  9  2  1  0  0  0  0
  9  4  2  0  0  0  0
 10  5  2  0  0  0  0
 10  6  1  0  0  0  0
 11  3  1  0  0  0  0
 12  4  1  0  0  0  0
 12 11  2  0  0  0  0
 13  5  1  0  0  0  0
 14  6  2  0  0  0  0
 15  7  1  0  0  0  0
 16 13  2  0  0  0  0
 16 14  1  0  0  0  0
 17  8  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  9  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 25  1  0  0  0  0
 28  7  1  0  0  0  0
 29 10  1  0  0  0  0
 30 11  1  0  0  0  0
 31 12  1  0  0  0  0
 32 13  1  0  0  0  0
 33 17  1  0  0  0  0
 34 18  1  0  0  0  0
 35 19  2  0  0  0  0
 36 20  1  0  0  0  0
 37 21  1  0  0  0  0
 38 22  1  0  0  0  0
 39  8  1  0  0  0  0
 39 27  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 27  1  0  0  0  0
 43 25  1  0  0  0  0
 43 26  1  0  0  0  0
M  END

HMDB0040486
     RDKit          3D
Quercetin 3-(2-glucosylrhamnoside)
 73 77  0  0  0  0  0  0  0  0999 V2000
   -0.5496    3.6938    3.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0335    2.7444    1.9687 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0107    1.9567    1.5880 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1683    1.2926    0.4391 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3991   -0.0334    0.5520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5507   -0.3816   -0.0722 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7839   -0.3647    0.5113 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0833   -0.0025    1.8825 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1358    0.0578    2.8447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4155    0.4467    4.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6955    0.7862    4.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0132    1.1812    5.8389 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6714    0.7293    3.5591 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9638    1.0740    3.9267 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3803    0.3458    2.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8687   -0.7118   -0.2071 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8557   -1.0756   -1.4342 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0687   -1.4058   -2.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0573   -1.7917   -3.3484 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2659   -2.1272   -3.9767 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848   -1.8539   -4.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6569   -1.5235   -3.4331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5083   -1.5962   -4.1509 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6452   -1.1295   -2.1136 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5106   -0.7808   -1.4180 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4096   -0.8129   -1.9736 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5721    1.2157   -0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4020    0.3408    0.5362 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8993   -0.6687   -0.2845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2726   -0.6024   -0.4284 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7416   -1.4208   -1.4426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5812   -0.6939   -2.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3071    0.5078   -2.7634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0275   -2.7289   -1.5382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9446   -3.7195   -1.8705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4987   -3.0752   -0.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9561   -4.3503   -0.2258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4387   -2.0273    0.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2814   -2.0780    1.5697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1825    2.6177   -0.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1669    3.0856   -1.5278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4886    3.5508    0.7532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3317    4.0117    0.1288 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0382    3.0918    3.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1075    4.4292    2.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4045    4.1727    3.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8957    2.1343    2.3496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5006    1.8000   -0.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0822   -0.2187    2.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6298    0.4819    4.9028 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3103    1.2272    6.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2425    1.3600    4.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1636    0.3085    1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0048   -1.3535   -1.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8085   -1.4102   -4.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583   -2.1559   -5.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5931   -1.4284   -3.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5061    0.8812   -1.1652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4619   -0.4886   -1.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8370   -1.6117   -1.3536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5354   -0.4643   -3.0050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9556   -1.3526   -3.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0105    0.9898   -3.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2188   -2.7323   -2.2798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7386   -3.7118   -1.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3275   -3.0371    0.5827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3616   -4.5289    0.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5234   -2.3144   -0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0692   -1.1385    1.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2416    2.5504    0.0961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7431    2.4571   -2.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0952    4.4208    1.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4047    4.9597   -0.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  2  0
  7 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  2  0
  4 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 31 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 27 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 42  2  1  0
 25  6  1  0
 38 29  1  0
 15  8  1  0
 24 17  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  0
  4 48  1  0
  9 49  1  0
 10 50  1  0
 12 51  1  0
 14 52  1  0
 15 53  1  0
 18 54  1  0
 20 55  1  0
 21 56  1  0
 23 57  1  0
 27 58  1  0
 29 59  1  0
 31 60  1  0
 32 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
 40 70  1  0
 41 71  1  0
 42 72  1  0
 43 73  1  0
M  END


  Mrv0541 05061311522D          

 43 47  0  0  0  0            999 V2000
    1.4289   -4.1250    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
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    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
    4.2868    0.0000    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    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
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    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
    5.7158   -2.4750    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
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    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
    6.4302   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    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
    7.1447   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    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
    5.0013   -3.7125    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
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  8  1  1  0  0  0  0
  9  2  1  0  0  0  0
  9  4  2  0  0  0  0
 10  5  2  0  0  0  0
 10  6  1  0  0  0  0
 11  3  1  0  0  0  0
 12  4  1  0  0  0  0
 12 11  2  0  0  0  0
 13  5  1  0  0  0  0
 14  6  2  0  0  0  0
 15  7  1  0  0  0  0
 16 13  2  0  0  0  0
 16 14  1  0  0  0  0
 17  8  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  9  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 25  1  0  0  0  0
 28  7  1  0  0  0  0
 29 10  1  0  0  0  0
 30 11  1  0  0  0  0
 31 12  1  0  0  0  0
 32 13  1  0  0  0  0
 33 17  1  0  0  0  0
 34 18  1  0  0  0  0
 35 19  2  0  0  0  0
 36 20  1  0  0  0  0
 37 21  1  0  0  0  0
 38 22  1  0  0  0  0
 39  8  1  0  0  0  0
 39 27  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 27  1  0  0  0  0
 43 25  1  0  0  0  0
 43 26  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0040486

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1OC(OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H30O16/c1-8-17(33)21(37)25(43-26-22(38)20(36)18(34)15(7-28)41-26)27(39-8)42-24-19(35)16-13(32)5-10(29)6-14(16)40-23(24)9-2-3-11(30)12(31)4-9/h2-6,8,15,17-18,20-22,25-34,36-38H,7H2,1H3

> <INCHI_KEY>
DFNXNCCYQRPZMD-UHFFFAOYSA-N

> <FORMULA>
C27H30O16

> <MOLECULAR_WEIGHT>
610.5175

> <EXACT_MASS>
610.153384912

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_AVERAGE_POLARIZABILITY>
57.715552892174635

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
0.18

> <JCHEM_LOGP>
-0.8687609749999999

> <ALOGPS_LOGS>
-2.12

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.451121037514051

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.433960689910189

> <JCHEM_PKA_STRONGEST_BASIC>
-3.648377595763173

> <JCHEM_POLAR_SURFACE_AREA>
265.52

> <JCHEM_REFRACTIVITY>
140.14509999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.68e+00 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0040486
     RDKit          3D
Quercetin 3-(2-glucosylrhamnoside)
 73 77  0  0  0  0  0  0  0  0999 V2000
   -0.5496    3.6938    3.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0335    2.7444    1.9687 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0107    1.9567    1.5880 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1683    1.2926    0.4391 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3991   -0.0334    0.5520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5507   -0.3816   -0.0722 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7839   -0.3647    0.5113 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0833   -0.0025    1.8825 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1358    0.0578    2.8447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4155    0.4467    4.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6955    0.7862    4.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0132    1.1812    5.8389 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6714    0.7293    3.5591 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9638    1.0740    3.9267 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3803    0.3458    2.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8687   -0.7118   -0.2071 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8557   -1.0756   -1.4342 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0687   -1.4058   -2.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0573   -1.7917   -3.3484 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2659   -2.1272   -3.9767 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848   -1.8539   -4.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6569   -1.5235   -3.4331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5083   -1.5962   -4.1509 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6452   -1.1295   -2.1136 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5106   -0.7808   -1.4180 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4096   -0.8129   -1.9736 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5721    1.2157   -0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4020    0.3408    0.5362 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8993   -0.6687   -0.2845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2726   -0.6024   -0.4284 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7416   -1.4208   -1.4426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5812   -0.6939   -2.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3071    0.5078   -2.7634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0275   -2.7289   -1.5382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9446   -3.7195   -1.8705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4987   -3.0752   -0.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9561   -4.3503   -0.2258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4387   -2.0273    0.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2814   -2.0780    1.5697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1825    2.6177   -0.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1669    3.0856   -1.5278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4886    3.5508    0.7532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3317    4.0117    0.1288 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0382    3.0918    3.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1075    4.4292    2.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4045    4.1727    3.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8957    2.1343    2.3496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5006    1.8000   -0.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0822   -0.2187    2.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6298    0.4819    4.9028 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3103    1.2272    6.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2425    1.3600    4.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1636    0.3085    1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0048   -1.3535   -1.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8085   -1.4102   -4.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583   -2.1559   -5.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5931   -1.4284   -3.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5061    0.8812   -1.1652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4619   -0.4886   -1.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8370   -1.6117   -1.3536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5354   -0.4643   -3.0050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9556   -1.3526   -3.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0105    0.9898   -3.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2188   -2.7323   -2.2798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7386   -3.7118   -1.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3275   -3.0371    0.5827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3616   -4.5289    0.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5234   -2.3144   -0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0692   -1.1385    1.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2416    2.5504    0.0961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7431    2.4571   -2.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0952    4.4208    1.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4047    4.9597   -0.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  2  0
  7 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  2  0
  4 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 31 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 27 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 42  2  1  0
 25  6  1  0
 38 29  1  0
 15  8  1  0
 24 17  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  0
  4 48  1  0
  9 49  1  0
 10 50  1  0
 12 51  1  0
 14 52  1  0
 15 53  1  0
 18 54  1  0
 20 55  1  0
 21 56  1  0
 23 57  1  0
 27 58  1  0
 29 59  1  0
 31 60  1  0
 32 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
 40 70  1  0
 41 71  1  0
 42 72  1  0
 43 73  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       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000  -3.080   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      10.669  -7.700   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       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.669  -4.620   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       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      12.003 -10.010   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      13.337  -7.700   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      13.337  -4.620   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       4.001  -5.390   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       9.336  -6.930   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
HETATM   43  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
CONECT    1    8                                                            
CONECT    2    3    9                                                       
CONECT    3    2   11                                                       
CONECT    4    9   12                                                       
CONECT    5   10   13                                                       
CONECT    6   10   14                                                       
CONECT    7   15   28                                                       
CONECT    8    1   17   39                                                  
CONECT    9    2    4   23                                                  
CONECT   10    5    6   29                                                  
CONECT   11    3   12   30                                                  
CONECT   12    4   11   31                                                  
CONECT   13    5   16   32                                                  
CONECT   14    6   16   40                                                  
CONECT   15    7   18   41                                                  
CONECT   16   13   14   19                                                  
CONECT   17    8   21   33                                                  
CONECT   18   15   20   34                                                  
CONECT   19   16   24   35                                                  
CONECT   20   18   22   36                                                  
CONECT   21   17   25   37                                                  
CONECT   22   20   26   38                                                  
CONECT   23    9   24   40                                                  
CONECT   24   19   23   42                                                  
CONECT   25   21   27   43                                                  
CONECT   26   22   41   43                                                  
CONECT   27   25   39   42                                                  
CONECT   28    7                                                            
CONECT   29   10                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   13                                                            
CONECT   33   17                                                            
CONECT   34   18                                                            
CONECT   35   19                                                            
CONECT   36   20                                                            
CONECT   37   21                                                            
CONECT   38   22                                                            
CONECT   39    8   27                                                       
CONECT   40   14   23                                                       
CONECT   41   15   26                                                       
CONECT   42   24   27                                                       
CONECT   43   25   26                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

COMPND    HMDB0040486
HETATM    1  C1  UNL     1      -0.550   3.694   3.055  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.034   2.744   1.969  1.00  0.00           C  
HETATM    3  O1  UNL     1       0.011   1.957   1.588  1.00  0.00           O  
HETATM    4  C3  UNL     1      -0.168   1.293   0.439  1.00  0.00           C  
HETATM    5  O2  UNL     1       0.399  -0.033   0.552  1.00  0.00           O  
HETATM    6  C4  UNL     1       1.551  -0.382  -0.072  1.00  0.00           C  
HETATM    7  C5  UNL     1       2.784  -0.365   0.511  1.00  0.00           C  
HETATM    8  C6  UNL     1       3.083  -0.002   1.882  1.00  0.00           C  
HETATM    9  C7  UNL     1       2.136   0.058   2.845  1.00  0.00           C  
HETATM   10  C8  UNL     1       2.416   0.447   4.164  1.00  0.00           C  
HETATM   11  C9  UNL     1       3.696   0.786   4.526  1.00  0.00           C  
HETATM   12  O3  UNL     1       4.013   1.181   5.839  1.00  0.00           O  
HETATM   13  C10 UNL     1       4.671   0.729   3.559  1.00  0.00           C  
HETATM   14  O4  UNL     1       5.964   1.074   3.927  1.00  0.00           O  
HETATM   15  C11 UNL     1       4.380   0.346   2.269  1.00  0.00           C  
HETATM   16  O5  UNL     1       3.869  -0.712  -0.207  1.00  0.00           O  
HETATM   17  C12 UNL     1       3.856  -1.076  -1.434  1.00  0.00           C  
HETATM   18  C13 UNL     1       5.069  -1.406  -2.047  1.00  0.00           C  
HETATM   19  C14 UNL     1       5.057  -1.792  -3.348  1.00  0.00           C  
HETATM   20  O6  UNL     1       6.266  -2.127  -3.977  1.00  0.00           O  
HETATM   21  C15 UNL     1       3.885  -1.854  -4.037  1.00  0.00           C  
HETATM   22  C16 UNL     1       2.657  -1.524  -3.433  1.00  0.00           C  
HETATM   23  O7  UNL     1       1.508  -1.596  -4.151  1.00  0.00           O  
HETATM   24  C17 UNL     1       2.645  -1.129  -2.114  1.00  0.00           C  
HETATM   25  C18 UNL     1       1.511  -0.781  -1.418  1.00  0.00           C  
HETATM   26  O8  UNL     1       0.410  -0.813  -1.974  1.00  0.00           O  
HETATM   27  C19 UNL     1      -1.572   1.216  -0.111  1.00  0.00           C  
HETATM   28  O9  UNL     1      -2.402   0.341   0.536  1.00  0.00           O  
HETATM   29  C20 UNL     1      -2.899  -0.669  -0.285  1.00  0.00           C  
HETATM   30  O10 UNL     1      -4.273  -0.602  -0.428  1.00  0.00           O  
HETATM   31  C21 UNL     1      -4.742  -1.421  -1.443  1.00  0.00           C  
HETATM   32  C22 UNL     1      -4.581  -0.694  -2.765  1.00  0.00           C  
HETATM   33  O11 UNL     1      -5.307   0.508  -2.763  1.00  0.00           O  
HETATM   34  C23 UNL     1      -4.028  -2.729  -1.538  1.00  0.00           C  
HETATM   35  O12 UNL     1      -4.945  -3.719  -1.871  1.00  0.00           O  
HETATM   36  C24 UNL     1      -3.499  -3.075  -0.156  1.00  0.00           C  
HETATM   37  O13 UNL     1      -2.956  -4.350  -0.226  1.00  0.00           O  
HETATM   38  C25 UNL     1      -2.439  -2.027   0.173  1.00  0.00           C  
HETATM   39  O14 UNL     1      -2.281  -2.078   1.570  1.00  0.00           O  
HETATM   40  C26 UNL     1      -2.182   2.618  -0.222  1.00  0.00           C  
HETATM   41  O15 UNL     1      -2.167   3.086  -1.528  1.00  0.00           O  
HETATM   42  C27 UNL     1      -1.489   3.551   0.753  1.00  0.00           C  
HETATM   43  O16 UNL     1      -0.332   4.012   0.129  1.00  0.00           O  
HETATM   44  H1  UNL     1       0.038   3.092   3.784  1.00  0.00           H  
HETATM   45  H2  UNL     1       0.108   4.429   2.530  1.00  0.00           H  
HETATM   46  H3  UNL     1      -1.405   4.173   3.538  1.00  0.00           H  
HETATM   47  H4  UNL     1      -1.896   2.134   2.350  1.00  0.00           H  
HETATM   48  H5  UNL     1       0.501   1.800  -0.334  1.00  0.00           H  
HETATM   49  H6  UNL     1       1.082  -0.219   2.679  1.00  0.00           H  
HETATM   50  H7  UNL     1       1.630   0.482   4.903  1.00  0.00           H  
HETATM   51  H8  UNL     1       3.310   1.227   6.559  1.00  0.00           H  
HETATM   52  H9  UNL     1       6.242   1.360   4.834  1.00  0.00           H  
HETATM   53  H10 UNL     1       5.164   0.309   1.526  1.00  0.00           H  
HETATM   54  H11 UNL     1       6.005  -1.354  -1.487  1.00  0.00           H  
HETATM   55  H12 UNL     1       6.809  -1.410  -4.455  1.00  0.00           H  
HETATM   56  H13 UNL     1       3.858  -2.156  -5.064  1.00  0.00           H  
HETATM   57  H14 UNL     1       0.593  -1.428  -3.963  1.00  0.00           H  
HETATM   58  H15 UNL     1      -1.506   0.881  -1.165  1.00  0.00           H  
HETATM   59  H16 UNL     1      -2.462  -0.489  -1.289  1.00  0.00           H  
HETATM   60  H17 UNL     1      -5.837  -1.612  -1.354  1.00  0.00           H  
HETATM   61  H18 UNL     1      -3.535  -0.464  -3.005  1.00  0.00           H  
HETATM   62  H19 UNL     1      -4.956  -1.353  -3.598  1.00  0.00           H  
HETATM   63  H20 UNL     1      -5.010   0.990  -3.598  1.00  0.00           H  
HETATM   64  H21 UNL     1      -3.219  -2.732  -2.280  1.00  0.00           H  
HETATM   65  H22 UNL     1      -5.739  -3.712  -1.265  1.00  0.00           H  
HETATM   66  H23 UNL     1      -4.328  -3.037   0.583  1.00  0.00           H  
HETATM   67  H24 UNL     1      -2.362  -4.529   0.548  1.00  0.00           H  
HETATM   68  H25 UNL     1      -1.523  -2.314  -0.362  1.00  0.00           H  
HETATM   69  H26 UNL     1      -2.069  -1.138   1.837  1.00  0.00           H  
HETATM   70  H27 UNL     1      -3.242   2.550   0.096  1.00  0.00           H  
HETATM   71  H28 UNL     1      -1.743   2.457  -2.162  1.00  0.00           H  
HETATM   72  H29 UNL     1      -2.095   4.421   1.028  1.00  0.00           H  
HETATM   73  H30 UNL     1      -0.405   4.960  -0.152  1.00  0.00           H  
CONECT    1    2   44   45   46
CONECT    2    3   42   47
CONECT    3    4
CONECT    4    5   27   48
CONECT    5    6
CONECT    6    7    7   25
CONECT    7    8   16
CONECT    8    9    9   15
CONECT    9   10   49
CONECT   10   11   11   50
CONECT   11   12   13
CONECT   12   51
CONECT   13   14   15   15
CONECT   14   52
CONECT   15   53
CONECT   16   17
CONECT   17   18   18   24
CONECT   18   19   54
CONECT   19   20   21   21
CONECT   20   55
CONECT   21   22   56
CONECT   22   23   24   24
CONECT   23   57
CONECT   24   25
CONECT   25   26   26
CONECT   27   28   40   58
CONECT   28   29
CONECT   29   30   38   59
CONECT   30   31
CONECT   31   32   34   60
CONECT   32   33   61   62
CONECT   33   63
CONECT   34   35   36   64
CONECT   35   65
CONECT   36   37   38   66
CONECT   37   67
CONECT   38   39   68
CONECT   39   69
CONECT   40   41   42   70
CONECT   41   71
CONECT   42   43   72
CONECT   43   73
END

HMDB0040486
     RDKit          3D
Quercetin 3-(2-glucosylrhamnoside)
 73 77  0  0  0  0  0  0  0  0999 V2000
   -0.5496    3.6938    3.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0335    2.7444    1.9687 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0107    1.9567    1.5880 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1683    1.2926    0.4391 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3991   -0.0334    0.5520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5507   -0.3816   -0.0722 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7839   -0.3647    0.5113 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0833   -0.0025    1.8825 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1358    0.0578    2.8447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4155    0.4467    4.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6955    0.7862    4.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0132    1.1812    5.8389 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6714    0.7293    3.5591 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9638    1.0740    3.9267 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3803    0.3458    2.2689 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8687   -0.7118   -0.2071 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8557   -1.0756   -1.4342 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0687   -1.4058   -2.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0573   -1.7917   -3.3484 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2659   -2.1272   -3.9767 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8848   -1.8539   -4.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6569   -1.5235   -3.4331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5083   -1.5962   -4.1509 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6452   -1.1295   -2.1136 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5106   -0.7808   -1.4180 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4096   -0.8129   -1.9736 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5721    1.2157   -0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4020    0.3408    0.5362 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8993   -0.6687   -0.2845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2726   -0.6024   -0.4284 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7416   -1.4208   -1.4426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5812   -0.6939   -2.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3071    0.5078   -2.7634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0275   -2.7289   -1.5382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9446   -3.7195   -1.8705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4987   -3.0752   -0.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9561   -4.3503   -0.2258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4387   -2.0273    0.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2814   -2.0780    1.5697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1825    2.6177   -0.2220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1669    3.0856   -1.5278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4886    3.5508    0.7532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3317    4.0117    0.1288 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0382    3.0918    3.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1075    4.4292    2.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4045    4.1727    3.5384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8957    2.1343    2.3496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5006    1.8000   -0.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0822   -0.2187    2.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6298    0.4819    4.9028 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3103    1.2272    6.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2425    1.3600    4.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1636    0.3085    1.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0048   -1.3535   -1.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8085   -1.4102   -4.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8583   -2.1559   -5.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5931   -1.4284   -3.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5061    0.8812   -1.1652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4619   -0.4886   -1.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8370   -1.6117   -1.3536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5354   -0.4643   -3.0050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9556   -1.3526   -3.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0105    0.9898   -3.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2188   -2.7323   -2.2798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7386   -3.7118   -1.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3275   -3.0371    0.5827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3616   -4.5289    0.5480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5234   -2.3144   -0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0692   -1.1385    1.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2416    2.5504    0.0961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7431    2.4571   -2.1622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0952    4.4208    1.0278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4047    4.9597   -0.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  2  0
  7 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  2  0
  4 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 31 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 27 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 42  2  1  0
 25  6  1  0
 38 29  1  0
 15  8  1  0
 24 17  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  0
  4 48  1  0
  9 49  1  0
 10 50  1  0
 12 51  1  0
 14 52  1  0
 15 53  1  0
 18 54  1  0
 20 55  1  0
 21 56  1  0
 23 57  1  0
 27 58  1  0
 29 59  1  0
 31 60  1  0
 32 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
 40 70  1  0
 41 71  1  0
 42 72  1  0
 43 73  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Quercetin 3-glucosyl-(1->2)-rhamnoside	HMDB

Chemical Formula

C₂₇H₃₀O₁₆

Average Molecular Weight

610.5175

Monoisotopic Molecular Weight

610.153384912

IUPAC Name

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

Traditional Name

3-[(4,5-dihydroxy-6-methyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

CAS Registry Number

143016-74-4

SMILES

CC1OC(OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O

InChI Identifier

InChI=1S/C27H30O16/c1-8-17(33)21(37)25(43-26-22(38)20(36)18(34)15(7-28)41-26)27(39-8)42-24-19(35)16-13(32)5-10(29)6-14(16)40-23(24)9-2-3-11(30)12(31)4-9/h2-6,8,15,17-18,20-22,25-34,36-38H,7H2,1H3

InChI Key

DFNXNCCYQRPZMD-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-3-O-glycosides

Alternative Parents

Substituents

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0040486)
Cytoplasm (HMDB: HMDB0040486)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0040486)

Source

Exogenous

Food

Food (HMDB: HMDB0040486)

Herb and spice

Other seed

Ginkgo nuts (FooDB: FOOD00367)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Endogenous

Plant

Plant (HMDB: HMDB0040486)

Not Available

Nutrient (HMDB: HMDB0040486)

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	4.68 g/L	ALOGPS
logP	0.18	ALOGPS
logP	-0.87	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	6.43	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	265.52 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	140.15 m³·mol⁻¹	ChemAxon
Polarizability	57.72 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	226.649	30932474
DeepCCS	[M-H]-	224.637	30932474
DeepCCS	[M-2H]-	257.876	30932474
DeepCCS	[M+Na]+	232.39	30932474
AllCCS	[M+H]+	231.9	32859911
AllCCS	[M+H-H2O]+	230.7	32859911
AllCCS	[M+NH4]+	233.1	32859911
AllCCS	[M+Na]+	233.4	32859911
AllCCS	[M-H]-	228.2	32859911
AllCCS	[M+Na-2H]-	230.3	32859911
AllCCS	[M+HCOO]-	232.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Quercetin 3-(2-glucosylrhamnoside)	CC1OC(OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5961.4	Standard polar	33892256
Quercetin 3-(2-glucosylrhamnoside)	CC1OC(OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5243.3	Standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside)	CC1OC(OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC(O)=C(O)C=C2)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5617.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #1	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5550.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #10	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5501.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #2	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5531.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #3	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5543.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #4	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5550.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #5	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5481.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #6	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5503.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #7	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5502.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #8	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5500.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TMS,isomer #9	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5515.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #1	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5436.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #10	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5420.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #11	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5404.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #12	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5415.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #13	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5419.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #14	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5402.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #15	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5415.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #16	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5432.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #17	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5429.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #18	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5412.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #19	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5391.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #2	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5420.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #20	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5391.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #21	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5373.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #22	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5391.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #23	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5405.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #24	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5405.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #25	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5411.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #26	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5410.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #27	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5395.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #28	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5408.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #29	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5422.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #3	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5425.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #30	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5422.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #31	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5402.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #32	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5399.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #33	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5400.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #34	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5410.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #35	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5402.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #36	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5415.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #37	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5395.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #38	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5408.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #39	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5404.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #4	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5426.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #40	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5413.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #41	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5410.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #42	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5407.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #43	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5422.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #44	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5407.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #45	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5442.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #5	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5432.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #6	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5420.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #7	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5434.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #8	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5447.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TMS,isomer #9	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5440.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #1	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5303.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #10	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5251.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #100	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5273.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #101	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5278.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #102	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5279.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #103	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5279.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #104	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5278.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #105	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5269.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #106	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5266.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #107	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5268.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #108	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5273.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #109	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5272.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #11	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5261.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #110	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5285.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #111	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5289.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #112	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5280.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #113	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5281.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #114	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5269.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #115	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5268.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #116	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5289.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #117	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5281.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #118	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5280.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #119	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5279.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #12	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5214.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #120	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5285.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #13	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5254.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #14	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5245.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #15	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5257.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #16	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5279.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #17	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5295.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #18	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5252.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #19	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5285.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #2	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5263.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #20	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5290.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #21	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5294.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #22	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5307.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #23	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5281.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #24	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5298.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #25	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5295.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #26	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5295.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #27	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5305.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #28	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5289.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #29	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5315.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #3	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5272.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #30	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5316.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #31	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5302.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #32	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5281.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #33	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5286.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #34	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5307.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #35	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5303.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #36	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5321.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #37	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5268.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #38	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5235.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #39	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5251.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #4	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5284.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #40	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5202.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #41	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5242.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #42	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5240.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #43	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5250.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #44	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5213.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #45	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5224.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #46	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5172.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #47	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5216.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #48	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5212.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #49	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5223.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #5	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5240.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #50	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5274.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #51	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5245.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #52	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5261.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #53	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5266.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #54	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5268.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #55	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5265.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #56	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5257.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #57	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5281.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #58	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5284.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #59	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5261.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #6	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5280.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #60	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5242.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #61	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5248.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #62	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5267.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #63	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5267.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #64	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5294.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #65	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5259.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #66	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5277.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #67	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5232.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #68	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5264.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #69	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5273.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #7	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5270.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #70	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5283.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #71	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5232.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #72	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5202.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #73	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5223.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #74	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5218.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #75	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5222.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #76	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5222.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #77	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5207.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #78	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5230.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #79	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5234.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #8	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5281.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #80	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5221.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #81	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5188.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #82	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5197.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #83	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5223.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #84	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5223.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #85	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5250.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #86	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5255.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #87	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5227.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #88	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5246.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #89	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5242.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #9	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5239.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #90	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5248.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #91	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5247.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #92	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5235.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #93	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5254.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #94	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5260.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #95	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5247.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #96	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5214.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #97	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5225.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #98	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5248.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),3TMS,isomer #99	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5249.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #1	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5125.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #10	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5031.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #100	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5057.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #101	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5014.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #102	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5028.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #103	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5050.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #104	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5066.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #105	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5088.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #106	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5076.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #107	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5015.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #108	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5049.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #109	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5025.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #11	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5085.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #110	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5041.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #111	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5041.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #112	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5035.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #113	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5046.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #114	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5061.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #115	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5036.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #116	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	4985.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #117	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5002.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #118	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5028.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #119	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5043.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #12	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5067.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #120	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5068.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #121	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5121.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #122	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5123.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #123	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5118.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #124	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5132.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #125	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5100.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #126	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5079.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #127	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5088.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #128	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5095.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #129	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5107.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #13	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5088.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #130	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5120.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #131	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5118.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #132	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5103.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #133	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5113.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #134	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5086.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #135	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5097.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #136	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5138.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #137	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5091.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #138	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5098.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #139	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5097.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #14	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5133.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #140	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5112.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #141	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5132.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #142	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5086.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #143	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5110.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #144	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5093.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #145	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5105.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #146	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5110.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #147	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5103.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #148	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5114.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #149	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5125.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #15	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5078.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #150	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5101.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #151	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5067.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #152	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5080.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #153	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5099.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #154	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5108.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #155	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5133.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #156	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5082.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #157	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5085.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #158	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5075.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #159	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5092.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #16	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5115.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #160	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5062.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #161	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5022.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #162	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5041.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #163	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5047.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #164	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5063.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #165	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5077.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #166	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5079.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #167	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5044.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #168	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5062.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #169	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5033.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #17	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5088.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #170	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5049.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #171	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5090.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #172	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5035.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #173	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5052.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #174	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5042.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #175	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5066.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #176	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5098.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #177	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5102.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #178	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5092.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #179	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5109.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #18	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5108.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #180	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5079.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #181	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5042.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #182	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5060.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #183	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5066.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #184	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5083.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #185	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5095.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #186	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5096.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #187	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5064.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #188	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5084.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #189	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5055.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #19	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5099.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #190	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5071.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #191	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5106.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #192	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5056.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #193	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5073.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #194	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5060.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #195	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5084.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #196	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5161.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #197	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5131.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #198	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5147.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #199	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5138.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #2	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5136.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #20	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5096.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #200	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5152.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #201	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5158.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #202	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5114.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #203	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5129.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #204	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5127.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #205	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5138.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #206	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5127.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #207	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5138.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #208	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5139.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #209	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5127.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #21	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5104.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #210	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5125.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #22	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5121.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #23	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5094.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #24	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5052.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #25	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5068.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #26	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5089.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #27	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5106.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #28	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5123.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #29	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5063.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #3	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5155.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #30	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5076.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #31	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5007.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #32	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5062.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #33	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5044.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #34	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5063.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #35	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5116.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #36	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5060.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #37	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5097.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #38	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5068.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #39	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5087.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #4	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5100.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #40	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5080.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #41	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5075.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #42	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5085.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #43	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5101.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #44	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5075.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #45	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5030.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #46	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5045.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #47	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5070.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #48	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5084.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #49	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5107.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #5	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5148.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #50	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5152.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #51	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5108.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #52	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5129.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #53	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5115.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #54	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5128.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #55	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5133.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #56	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5116.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #57	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5137.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #58	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5148.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #59	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5121.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #6	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5127.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #60	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5084.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #61	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5096.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #62	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5116.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #63	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5125.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #64	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5149.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #65	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5158.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #66	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5163.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #67	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5158.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #68	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5172.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #69	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5143.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #7	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5140.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #70	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5122.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #71	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5134.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #72	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5141.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #73	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5153.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #74	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5166.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #75	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O	5157.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #76	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O	5143.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #77	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O[Si](C)(C)C	5157.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #78	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5132.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #79	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5144.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #8	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5085.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #80	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5177.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #81	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5134.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #82	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5145.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #83	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5139.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #84	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5156.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #85	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O	5094.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #86	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5118.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #87	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5058.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #88	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5107.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #89	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5091.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #9	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5100.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #90	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5105.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #91	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O	5095.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #92	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C2O)C(O)C1O	5038.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #93	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O[Si](C)(C)C)C(O)C1O	5071.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #94	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C)C1O	5047.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #95	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C	5065.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #96	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)C1O	5063.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #97	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)C1O	5057.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #98	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)C1O	5068.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),4TMS,isomer #99	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C	5083.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #1	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5734.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #10	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5731.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #2	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5712.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #3	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5719.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #4	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5733.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #5	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O)C1O	5686.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #6	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O	5736.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #7	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	5730.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #8	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5725.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),1TBDMS,isomer #9	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5737.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #1	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5796.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #10	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5773.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #11	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5745.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #12	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O)C1O	5761.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #13	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O	5777.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #14	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	5746.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #15	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5755.9	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #16	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5781.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #17	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5781.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #18	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5764.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #19	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O)C1O	5740.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #2	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5768.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #20	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O	5744.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #21	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	5708.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #22	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5716.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #23	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5755.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #24	CC1OC(OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5759.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #25	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O)C1O	5769.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #26	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O	5772.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #27	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	5739.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #28	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5745.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #29	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5783.3	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #3	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O	5775.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #30	CC1OC(OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5788.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #31	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O	5760.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #32	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	5754.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #33	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5754.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #34	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5773.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #35	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5772.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #36	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	5764.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #37	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5752.4	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #38	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5778.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #39	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5779.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #4	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO[Si](C)(C)C(C)(C)C)C(O)C(O)C2O)C(O)C1O	5790.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #40	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5755.6	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #41	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5757.5	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #42	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5760.0	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #43	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	5762.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #44	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	5760.1	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #45	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	5809.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #5	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)C1O	5797.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #6	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)C1O	5767.7	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #7	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)C1O	5777.2	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #8	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)C1O	5806.8	Semi standard non polar	33892256
Quercetin 3-(2-glucosylrhamnoside),2TBDMS,isomer #9	CC1OC(OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)C(OC2OC(CO)C(O)C(O)C2O)C(O)C1O[Si](C)(C)C(C)(C)C	5807.7	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-(2-glucosylrhamnoside) GC-MS (Non-derivatized) - 70eV, Positive	splash10-0596-7511190000-14529c004c1d2114369e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) GC-MS (1 TMS) - 70eV, Positive	splash10-0wt9-8511029000-ea4c01c68560189ece17	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) 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-(2-glucosylrhamnoside) GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0udi-1109100000-2e642b9edf1de854e440	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0udi-0009001000-b710e5d193bf04d69b96	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Negative-QTOF	splash10-0a4j-0033409000-a85195c947b3ba4af315	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0udi-0109100000-e7dcc48f7ec8f79d082a	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0udi-0009101000-15216ebac90fc6646c84	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0udi-1109100000-08e52f54d0b72a9f64bc	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0fk9-0093000000-be8e6d6486982ae1f587	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0a4i-0000009000-4dc4a9c006a62e56eabc	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Negative-QTOF	splash10-0a4i-0004009000-1f7264f2ceab1d786a2c	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0fk9-0093000000-5725561d7a64cdd4dbcd	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0w29-0009005000-e90093426db60aa8fa1f	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0a4i-0004009000-51cf8a501727cd5a653c	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0udi-1339000000-3b24e5400904adbf8f2b	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0udi-0009001000-4b2a9352b5018bea34df	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0a4i-0004009000-73af6f33cea7cf470325	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0w29-0009207000-aef45c63eec6ccd3bbc3	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0udi-1109100000-98e1a6f375e0ca47f02d	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0a4i-0000009000-4fbc79f407ce0902219a	2021-09-20	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 6V, Positive-QTOF	splash10-0fk9-0093000000-6c2f97a5c20c8296b710	2021-09-20	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 10V, Positive-QTOF	splash10-0udi-0229833000-aea5012536525bf66bcb	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 20V, Positive-QTOF	splash10-0udi-0249400000-e529b0e5c0b419fcdeea	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 40V, Positive-QTOF	splash10-0uds-0935100000-809bdc5d9c24065ffcf9	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 10V, Negative-QTOF	splash10-0pdi-2519635000-b1c09d6a6207cb467c4f	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 20V, Negative-QTOF	splash10-0ufr-2729310000-4b3534f9c5d5d20fc170	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 3-(2-glucosylrhamnoside) 40V, Negative-QTOF	splash10-0ufr-2914000000-ceb4e025ae1183827a36	2017-09-01	Wishart Lab	View Spectrum

NMR Spectra

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

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

FDB020245

KNApSAcK ID

C00005417

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

14238625

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for Quercetin 3-(2-glucosylrhamnoside) (HMDB0040486)

MOL for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

3D MOL for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

3D SDF for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

3D-SDF for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

PDB for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

3D PDB for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

SMILES for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

INCHI for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

Structure for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

3D Structure for HMDB0040486 (Quercetin 3-(2-glucosylrhamnoside))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra