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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 00:48:50 UTC

Update Date

2022-03-07 02:56:11 UTC

HMDB ID

HMDB0039383

Secondary Accession Numbers

HMDB39383

Metabolite Identification

Common Name

Quercetin 7-(rhamnosylglucoside)

Description

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

Structure

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


  Mrv0541 02241221082D          

 43 47  0  0  1  0            999 V2000
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 33 42  2  0  0  0  0
  2 42  1  0  0  0  0
 42 43  1  0  0  0  0
M  END

HMDB0039383
     RDKit          3D
Quercetin 7-(rhamnosylglucoside)
 73 77  0  0  0  0  0  0  0  0999 V2000
   -1.3411    2.4517    1.6659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1394    1.5671    2.5916 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0259    0.2585    2.1277 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6047   -1.0084   -0.8471 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2877   -1.5241   -1.3402 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8188   -0.6703   -2.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668    0.0213   -2.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6552    0.8190   -3.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8144    1.5379   -3.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
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 36  6  1  0
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 37 67  1  0
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 40 70  1  1
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 42 72  1  6
 43 73  1  0
M  END


  Mrv0541 02241221082D          

 43 47  0  0  1  0            999 V2000
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    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
  9 18  1  0  0  0  0
 18 19  1  6  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  6  0  0  0
 22 29  1  6  0  0  0
  7 30  1  0  0  0  0
 30 31  2  0  0  0  0
  3 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 34 41  1  0  0  0  0
 33 42  2  0  0  0  0
  2 42  1  0  0  0  0
 42 43  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0039383

> <DATABASE_NAME>
hmdb

> <SMILES>
C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2OC2=CC(O)=C3C(=O)C(O)=C(OC3=C2)C2=CC=C(O)C(O)=C2)[C@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H30O16/c1-8-17(32)20(35)23(38)26(39-8)43-25-21(36)18(33)15(7-28)42-27(25)40-10-5-13(31)16-14(6-10)41-24(22(37)19(16)34)9-2-3-11(29)12(30)4-9/h2-6,8,15,17-18,20-21,23,25-33,35-38H,7H2,1H3/t8-,15+,17-,18+,20+,21-,23+,25+,26-,27+/m0/s1

> <INCHI_KEY>
HIEKMCGJSNLAGG-MTKPOXERSA-N

> <FORMULA>
C27H30O16

> <MOLECULAR_WEIGHT>
610.5175

> <EXACT_MASS>
610.153384912

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_AVERAGE_POLARIZABILITY>
58.48678778762622

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-0.18

> <JCHEM_LOGP>
-0.8356943083333334

> <ALOGPS_LOGS>
-2.26

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.688974736027676

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.977498861400448

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6486921994064723

> <JCHEM_POLAR_SURFACE_AREA>
265.52

> <JCHEM_REFRACTIVITY>
139.87619999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.34e+00 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0039383
     RDKit          3D
Quercetin 7-(rhamnosylglucoside)
 73 77  0  0  0  0  0  0  0  0999 V2000
   -1.3411    2.4517    1.6659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1394    1.5671    2.5916 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0259    0.2585    2.1277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0437   -0.0727    1.2453 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7472   -1.2101    0.5005 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6047   -1.0084   -0.8471 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2877   -1.5241   -1.3402 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8188   -0.6703   -2.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668    0.0213   -2.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6552    0.8190   -3.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8144    1.5379   -3.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0815    2.3323   -4.7470 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7616    1.5048   -2.6230 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9102    2.2226   -2.7500 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1528    2.9440   -3.7769 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8559    2.1653   -1.7176 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0003    2.9022   -1.8777 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5649    1.3844   -0.6347 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4859    1.2693    0.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7453    1.7683    0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5423    1.6197    1.7029 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0799    0.9611    2.7897 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8235    0.7794    3.9576 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7966    0.4323    2.7532 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3022   -0.2475    3.8584 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0403    0.5915    1.6265 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4087    0.7078   -0.5863 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5098    0.7336   -1.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3201   -0.0033   -1.4011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3109   -2.7895   -1.8996 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0581   -3.7382   -1.2386 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1932   -4.9295   -2.1663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9383   -5.9439   -1.5707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4692   -3.2653   -0.9554 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6034   -3.1846    0.4278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6828   -1.8728   -1.5163 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4368   -1.9331   -2.8888 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4119   -0.1561    1.8721 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3506    0.0858    0.8659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5401    0.9432    2.8825 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8350    1.4991    2.7925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5787    2.0407    2.5465 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7268    3.0331    3.5189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4083    2.8240    2.1412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0258    1.9477    0.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    3.3555    1.3547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7410    1.7094    3.6156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0925    0.7705    0.5024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7268    0.0530   -1.1511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5511   -1.5232   -0.5002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0805    0.8513   -4.2858 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3816    2.3559   -5.4779 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1437    3.4468   -2.6987 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1537    2.2908   -0.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5223    2.0451    1.6784 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7546    1.1661    3.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8781   -0.3552    4.6877 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0319    0.1743    1.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1892   -0.5809   -0.5162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5501   -4.1026   -0.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2175   -5.2753   -2.5508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7838   -4.5850   -3.0481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3118   -6.5741   -2.2167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2537   -3.9397   -1.3309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3167   -3.7738    0.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6917   -1.5059   -1.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1566   -2.3950   -3.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5855   -1.1406    2.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0644   -0.5943    0.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4534    0.5884    3.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5052    0.7765    2.7708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8429    2.4929    1.5786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8527    3.4707    3.7278 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  2  0
 18 27  1  0
 27 28  1  0
 28 29  2  0
  7 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
  4 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 42  2  1  0
 36  6  1  0
 29  9  1  0
 28 13  1  0
 26 19  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  1
  4 48  1  6
  6 49  1  1
  7 50  1  1
 10 51  1  0
 12 52  1  0
 17 53  1  0
 20 54  1  0
 21 55  1  0
 23 56  1  0
 25 57  1  0
 26 58  1  0
 29 59  1  0
 31 60  1  1
 32 61  1  0
 32 62  1  0
 33 63  1  0
 34 64  1  6
 35 65  1  0
 36 66  1  6
 37 67  1  0
 38 68  1  1
 39 69  1  0
 40 70  1  1
 41 71  1  0
 42 72  1  6
 43 73  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      10.669  -4.620   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.003  -6.930   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.671  -6.930   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      16.004  -7.700   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      14.671  -5.390   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      16.004  -4.620   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4   31                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   30                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   18                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    9   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   27                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   20   28                                                  
CONECT   28   27                                                            
CONECT   29   22                                                            
CONECT   30    7   31                                                       
CONECT   31   30    3   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   42                                                  
CONECT   34   33   35   41                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   34                                                       
CONECT   42   33    2   43                                                  
CONECT   43   42                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

COMPND    HMDB0039383
HETATM    1  C1  UNL     1      -1.341   2.452   1.666  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.139   1.567   2.592  1.00  0.00           C  
HETATM    3  O1  UNL     1      -2.026   0.259   2.128  1.00  0.00           O  
HETATM    4  C3  UNL     1      -3.044  -0.073   1.245  1.00  0.00           C  
HETATM    5  O2  UNL     1      -2.747  -1.210   0.501  1.00  0.00           O  
HETATM    6  C4  UNL     1      -2.605  -1.008  -0.847  1.00  0.00           C  
HETATM    7  C5  UNL     1      -1.288  -1.524  -1.340  1.00  0.00           C  
HETATM    8  O3  UNL     1      -0.819  -0.670  -2.350  1.00  0.00           O  
HETATM    9  C6  UNL     1       0.367   0.021  -2.388  1.00  0.00           C  
HETATM   10  C7  UNL     1       0.655   0.819  -3.502  1.00  0.00           C  
HETATM   11  C8  UNL     1       1.814   1.538  -3.617  1.00  0.00           C  
HETATM   12  O4  UNL     1       2.081   2.332  -4.747  1.00  0.00           O  
HETATM   13  C9  UNL     1       2.762   1.505  -2.623  1.00  0.00           C  
HETATM   14  C10 UNL     1       3.910   2.223  -2.750  1.00  0.00           C  
HETATM   15  O5  UNL     1       4.153   2.944  -3.777  1.00  0.00           O  
HETATM   16  C11 UNL     1       4.856   2.165  -1.718  1.00  0.00           C  
HETATM   17  O6  UNL     1       6.000   2.902  -1.878  1.00  0.00           O  
HETATM   18  C12 UNL     1       4.565   1.384  -0.635  1.00  0.00           C  
HETATM   19  C13 UNL     1       5.486   1.269   0.479  1.00  0.00           C  
HETATM   20  C14 UNL     1       6.745   1.768   0.560  1.00  0.00           C  
HETATM   21  C15 UNL     1       7.542   1.620   1.703  1.00  0.00           C  
HETATM   22  C16 UNL     1       7.080   0.961   2.790  1.00  0.00           C  
HETATM   23  O7  UNL     1       7.824   0.779   3.958  1.00  0.00           O  
HETATM   24  C17 UNL     1       5.797   0.432   2.753  1.00  0.00           C  
HETATM   25  O8  UNL     1       5.302  -0.247   3.858  1.00  0.00           O  
HETATM   26  C18 UNL     1       5.040   0.592   1.627  1.00  0.00           C  
HETATM   27  O9  UNL     1       3.409   0.708  -0.586  1.00  0.00           O  
HETATM   28  C19 UNL     1       2.510   0.734  -1.518  1.00  0.00           C  
HETATM   29  C20 UNL     1       1.320  -0.003  -1.401  1.00  0.00           C  
HETATM   30  O10 UNL     1      -1.311  -2.789  -1.900  1.00  0.00           O  
HETATM   31  C21 UNL     1      -2.058  -3.738  -1.239  1.00  0.00           C  
HETATM   32  C22 UNL     1      -2.193  -4.930  -2.166  1.00  0.00           C  
HETATM   33  O11 UNL     1      -2.938  -5.944  -1.571  1.00  0.00           O  
HETATM   34  C23 UNL     1      -3.469  -3.265  -0.955  1.00  0.00           C  
HETATM   35  O12 UNL     1      -3.603  -3.185   0.428  1.00  0.00           O  
HETATM   36  C24 UNL     1      -3.683  -1.873  -1.516  1.00  0.00           C  
HETATM   37  O13 UNL     1      -3.437  -1.933  -2.889  1.00  0.00           O  
HETATM   38  C25 UNL     1      -4.412  -0.156   1.872  1.00  0.00           C  
HETATM   39  O14 UNL     1      -5.351   0.086   0.866  1.00  0.00           O  
HETATM   40  C26 UNL     1      -4.540   0.943   2.883  1.00  0.00           C  
HETATM   41  O15 UNL     1      -5.835   1.499   2.792  1.00  0.00           O  
HETATM   42  C27 UNL     1      -3.579   2.041   2.547  1.00  0.00           C  
HETATM   43  O16 UNL     1      -3.727   3.033   3.519  1.00  0.00           O  
HETATM   44  H1  UNL     1      -0.408   2.824   2.141  1.00  0.00           H  
HETATM   45  H2  UNL     1      -1.026   1.948   0.731  1.00  0.00           H  
HETATM   46  H3  UNL     1      -1.917   3.356   1.355  1.00  0.00           H  
HETATM   47  H4  UNL     1      -1.741   1.709   3.616  1.00  0.00           H  
HETATM   48  H5  UNL     1      -3.093   0.770   0.502  1.00  0.00           H  
HETATM   49  H6  UNL     1      -2.727   0.053  -1.151  1.00  0.00           H  
HETATM   50  H7  UNL     1      -0.551  -1.523  -0.500  1.00  0.00           H  
HETATM   51  H8  UNL     1      -0.081   0.851  -4.286  1.00  0.00           H  
HETATM   52  H9  UNL     1       1.382   2.356  -5.478  1.00  0.00           H  
HETATM   53  H10 UNL     1       6.144   3.447  -2.699  1.00  0.00           H  
HETATM   54  H11 UNL     1       7.154   2.291  -0.295  1.00  0.00           H  
HETATM   55  H12 UNL     1       8.522   2.045   1.678  1.00  0.00           H  
HETATM   56  H13 UNL     1       8.755   1.166   3.977  1.00  0.00           H  
HETATM   57  H14 UNL     1       5.878  -0.355   4.688  1.00  0.00           H  
HETATM   58  H15 UNL     1       4.032   0.174   1.607  1.00  0.00           H  
HETATM   59  H16 UNL     1       1.189  -0.581  -0.516  1.00  0.00           H  
HETATM   60  H17 UNL     1      -1.550  -4.103  -0.324  1.00  0.00           H  
HETATM   61  H18 UNL     1      -1.217  -5.275  -2.551  1.00  0.00           H  
HETATM   62  H19 UNL     1      -2.784  -4.585  -3.048  1.00  0.00           H  
HETATM   63  H20 UNL     1      -3.312  -6.574  -2.217  1.00  0.00           H  
HETATM   64  H21 UNL     1      -4.254  -3.940  -1.331  1.00  0.00           H  
HETATM   65  H22 UNL     1      -4.317  -3.774   0.779  1.00  0.00           H  
HETATM   66  H23 UNL     1      -4.692  -1.506  -1.351  1.00  0.00           H  
HETATM   67  H24 UNL     1      -4.157  -2.395  -3.377  1.00  0.00           H  
HETATM   68  H25 UNL     1      -4.586  -1.141   2.362  1.00  0.00           H  
HETATM   69  H26 UNL     1      -6.064  -0.594   0.830  1.00  0.00           H  
HETATM   70  H27 UNL     1      -4.453   0.588   3.928  1.00  0.00           H  
HETATM   71  H28 UNL     1      -6.505   0.776   2.771  1.00  0.00           H  
HETATM   72  H29 UNL     1      -3.843   2.493   1.579  1.00  0.00           H  
HETATM   73  H30 UNL     1      -2.853   3.471   3.728  1.00  0.00           H  
CONECT    1    2   44   45   46
CONECT    2    3   42   47
CONECT    3    4
CONECT    4    5   38   48
CONECT    5    6
CONECT    6    7   36   49
CONECT    7    8   30   50
CONECT    8    9
CONECT    9   10   10   29
CONECT   10   11   51
CONECT   11   12   13   13
CONECT   12   52
CONECT   13   14   28
CONECT   14   15   15   16
CONECT   16   17   18   18
CONECT   17   53
CONECT   18   19   27
CONECT   19   20   20   26
CONECT   20   21   54
CONECT   21   22   22   55
CONECT   22   23   24
CONECT   23   56
CONECT   24   25   26   26
CONECT   25   57
CONECT   26   58
CONECT   27   28
CONECT   28   29   29
CONECT   29   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   66
CONECT   37   67
CONECT   38   39   40   68
CONECT   39   69
CONECT   40   41   42   70
CONECT   41   71
CONECT   42   43   72
CONECT   43   73
END

HMDB0039383
     RDKit          3D
Quercetin 7-(rhamnosylglucoside)
 73 77  0  0  0  0  0  0  0  0999 V2000
   -1.3411    2.4517    1.6659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1394    1.5671    2.5916 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0259    0.2585    2.1277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0437   -0.0727    1.2453 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7472   -1.2101    0.5005 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6047   -1.0084   -0.8471 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2877   -1.5241   -1.3402 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8188   -0.6703   -2.3497 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668    0.0213   -2.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6552    0.8190   -3.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8144    1.5379   -3.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0815    2.3323   -4.7470 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7616    1.5048   -2.6230 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9102    2.2226   -2.7500 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1528    2.9440   -3.7769 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8559    2.1653   -1.7176 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0003    2.9022   -1.8777 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5649    1.3844   -0.6347 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4859    1.2693    0.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7453    1.7683    0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5423    1.6197    1.7029 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0799    0.9611    2.7897 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8235    0.7794    3.9576 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7966    0.4323    2.7532 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3022   -0.2475    3.8584 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0403    0.5915    1.6265 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4087    0.7078   -0.5863 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5098    0.7336   -1.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3201   -0.0033   -1.4011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3109   -2.7895   -1.8996 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0581   -3.7382   -1.2386 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1932   -4.9295   -2.1663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9383   -5.9439   -1.5707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4692   -3.2653   -0.9554 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6034   -3.1846    0.4278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6828   -1.8728   -1.5163 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4368   -1.9331   -2.8888 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4119   -0.1561    1.8721 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3506    0.0858    0.8659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5401    0.9432    2.8825 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8350    1.4991    2.7925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5787    2.0407    2.5465 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7268    3.0331    3.5189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4083    2.8240    2.1412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0258    1.9477    0.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    3.3555    1.3547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7410    1.7094    3.6156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0925    0.7705    0.5024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7268    0.0530   -1.1511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5511   -1.5232   -0.5002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0805    0.8513   -4.2858 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3816    2.3559   -5.4779 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1437    3.4468   -2.6987 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1537    2.2908   -0.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5223    2.0451    1.6784 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7546    1.1661    3.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8781   -0.3552    4.6877 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0319    0.1743    1.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1892   -0.5809   -0.5162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5501   -4.1026   -0.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2175   -5.2753   -2.5508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7838   -4.5850   -3.0481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3118   -6.5741   -2.2167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2537   -3.9397   -1.3309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3167   -3.7738    0.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6917   -1.5059   -1.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1566   -2.3950   -3.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5855   -1.1406    2.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0644   -0.5943    0.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4534    0.5884    3.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5052    0.7765    2.7708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8429    2.4929    1.5786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8527    3.4707    3.7278 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  2  0
 18 27  1  0
 27 28  1  0
 28 29  2  0
  7 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
  4 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 42  2  1  0
 36  6  1  0
 29  9  1  0
 28 13  1  0
 26 19  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  1
  4 48  1  6
  6 49  1  1
  7 50  1  1
 10 51  1  0
 12 52  1  0
 17 53  1  0
 20 54  1  0
 21 55  1  0
 23 56  1  0
 25 57  1  0
 26 58  1  0
 29 59  1  0
 31 60  1  1
 32 61  1  0
 32 62  1  0
 33 63  1  0
 34 64  1  6
 35 65  1  0
 36 66  1  6
 37 67  1  0
 38 68  1  1
 39 69  1  0
 40 70  1  1
 41 71  1  0
 42 72  1  6
 43 73  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₇H₃₀O₁₆

Average Molecular Weight

610.5175

Monoisotopic Molecular Weight

610.153384912

IUPAC Name

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

Traditional Name

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

CAS Registry Number

73432-00-5

SMILES

C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2OC2=CC(O)=C3C(=O)C(O)=C(OC3=C2)C2=CC=C(O)C(O)=C2)[C@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C27H30O16/c1-8-17(32)20(35)23(38)26(39-8)43-25-21(36)18(33)15(7-28)42-27(25)40-10-5-13(31)16-14(6-10)41-24(22(37)19(16)34)9-2-3-11(29)12(30)4-9/h2-6,8,15,17-18,20-21,23,25-33,35-38H,7H2,1H3/t8-,15+,17-,18+,20+,21-,23+,25+,26-,27+/m0/s1

InChI Key

HIEKMCGJSNLAGG-MTKPOXERSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0039383)
Cytoplasm (HMDB: HMDB0039383)

Fats and oils (FooDB: FOOD00864)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	3.34 g/L	ALOGPS
logP	-0.18	ALOGPS
logP	-0.84	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	7.98	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	265.52 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	139.88 m³·mol⁻¹	ChemAxon
Polarizability	58.49 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]+	229.965	30932474
DeepCCS	[M-H]-	227.955	30932474
DeepCCS	[M-2H]-	261.771	30932474
DeepCCS	[M+Na]+	236.039	30932474
AllCCS	[M+H]+	231.6	32859911
AllCCS	[M+H-H2O]+	230.5	32859911
AllCCS	[M+NH4]+	232.7	32859911
AllCCS	[M+Na]+	233.0	32859911
AllCCS	[M-H]-	227.4	32859911
AllCCS	[M+Na-2H]-	229.6	32859911
AllCCS	[M+HCOO]-	232.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Quercetin 7-(rhamnosylglucoside)	C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2OC2=CC(O)=C3C(=O)C(O)=C(OC3=C2)C2=CC=C(O)C(O)=C2)[C@H](O)[C@H](O)[C@H]1O	6089.1	Standard polar	33892256
Quercetin 7-(rhamnosylglucoside)	C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2OC2=CC(O)=C3C(=O)C(O)=C(OC3=C2)C2=CC=C(O)C(O)=C2)[C@H](O)[C@H](O)[C@H]1O	5088.9	Standard non polar	33892256
Quercetin 7-(rhamnosylglucoside)	C[C@@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]2OC2=CC(O)=C3C(=O)C(O)=C(OC3=C2)C2=CC=C(O)C(O)=C2)[C@H](O)[C@H](O)[C@H]1O	5537.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #1	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5257.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #10	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5267.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #2	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5245.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #3	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5261.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #4	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5263.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #5	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5208.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #6	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5300.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #7	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5257.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #8	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5254.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TMS,isomer #9	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5261.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #1	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5122.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #10	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5113.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #11	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5081.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #12	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5113.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #13	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5082.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #14	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5142.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #15	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5110.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #16	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5106.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #17	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5112.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #18	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5123.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #19	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5089.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #2	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5086.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #20	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5134.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #21	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5099.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #22	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5134.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #23	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5130.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #24	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5137.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #25	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5097.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #26	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5128.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #27	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5100.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #28	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5120.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #29	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5115.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #3	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5119.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #30	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5129.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #31	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5078.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #32	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5056.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #33	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5089.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #34	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5090.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #35	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5098.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #36	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5116.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #37	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5128.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #38	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5119.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #39	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5138.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #4	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5087.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #40	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5097.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #41	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5086.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #42	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5108.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #43	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5126.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #44	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5122.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #45	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5128.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #5	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5136.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #6	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5132.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #7	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5122.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #8	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5115.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TMS,isomer #9	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5124.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #1	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4946.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #10	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4891.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #100	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5005.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #101	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4942.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #102	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4919.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #103	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4900.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #104	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4930.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #105	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4904.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #106	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4884.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #107	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4917.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #108	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4980.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #109	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4995.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #11	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4971.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #110	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4987.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #111	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4985.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #112	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4968.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #113	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4994.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #114	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4981.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #115	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4992.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #116	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4987.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #117	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4957.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #118	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4967.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #119	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4964.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #12	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4971.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #120	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5046.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #13	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4983.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #14	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4969.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #15	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4988.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #16	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4970.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #17	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4977.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #18	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4967.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #19	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4970.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #2	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4958.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #20	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4952.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #21	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4981.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #22	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4952.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #23	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4947.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #24	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4944.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #25	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4925.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #26	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4955.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #27	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5044.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #28	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5033.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #29	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5021.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #3	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4934.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #30	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5045.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #31	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5033.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #32	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5022.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #33	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5042.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #34	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5024.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #35	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5038.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #36	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5037.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #37	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4939.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #38	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4953.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #39	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4931.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #4	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4991.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #40	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5006.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #41	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4989.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #42	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4973.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #43	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5002.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #44	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4900.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #45	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4885.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #46	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4992.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #47	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4973.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #48	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4959.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #49	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4981.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #5	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4990.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #50	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4971.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #51	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4991.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #52	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4967.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #53	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4948.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #54	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4977.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #55	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4967.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #56	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4942.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #57	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4922.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #58	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4952.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #59	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5049.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #6	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4996.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #60	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5039.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #61	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5058.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #62	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5019.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #63	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5034.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #64	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5032.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #65	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4953.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #66	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4980.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #67	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4954.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #68	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5007.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #69	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4993.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #7	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4980.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #70	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5018.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #71	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4927.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #72	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4910.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #73	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4984.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #74	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4974.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #75	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4993.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #76	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4999.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #77	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4991.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #78	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4974.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #79	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5002.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #8	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5008.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #80	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4966.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #81	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4949.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #82	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4977.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #83	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5033.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #84	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5050.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #85	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5046.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #86	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4924.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #87	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4905.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #88	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4960.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #89	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4944.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #9	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4905.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #90	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4970.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #91	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4986.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #92	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4969.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #93	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4948.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #94	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4982.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #95	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4944.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #96	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4922.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #97	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4959.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #98	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4994.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),3TMS,isomer #99	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5011.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #1	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4791.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #10	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4848.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #100	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4940.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #101	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4917.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #102	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4955.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #103	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4904.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #104	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4919.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #105	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4912.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #106	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4840.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #107	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4829.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #108	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4801.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #109	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4778.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #11	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4841.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #110	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4814.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #111	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4816.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #112	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4790.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #113	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4767.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #114	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4802.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #115	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4930.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #116	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4909.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #117	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4943.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #118	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4896.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #119	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4913.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #12	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4824.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #120	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4907.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #121	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4901.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #122	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4884.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #123	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4861.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #124	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4901.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #125	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4899.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #126	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4880.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #127	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4912.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #128	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4872.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #129	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4880.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #13	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4860.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #130	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4873.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #131	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4874.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #132	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4854.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #133	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4889.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #134	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4849.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #135	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4855.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #136	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4852.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #137	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4984.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #138	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5000.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #139	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5000.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #14	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4833.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #140	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4970.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #141	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4812.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #142	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4801.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #143	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4875.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #144	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4855.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #145	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4892.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #146	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4874.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #147	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4864.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #148	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4842.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #149	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4879.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #15	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4835.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #150	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4843.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #151	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4821.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #152	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4859.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #153	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4928.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #154	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4946.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #155	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4941.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #156	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4857.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #157	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4830.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #158	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4808.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #159	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4841.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #16	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4822.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #160	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4818.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #161	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4795.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #162	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4830.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #163	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4915.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #164	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4934.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #165	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4929.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #166	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4905.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #167	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4881.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #168	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4920.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #169	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4898.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #17	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4805.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #170	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4911.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #171	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4904.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #172	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4878.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #173	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4887.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #174	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4885.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #175	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4990.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #176	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4844.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #177	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4803.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #178	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4791.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #179	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4825.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #18	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4842.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #180	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4791.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #181	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4777.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #182	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4812.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #183	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4859.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #184	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4878.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #185	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4871.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #186	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4880.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #187	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4862.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #188	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4896.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #189	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4855.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #19	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4933.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #190	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4864.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #191	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4861.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #192	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4835.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #193	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4844.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #194	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4843.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #195	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4936.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #196	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4858.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #197	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4838.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #198	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4872.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #199	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4820.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #2	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4780.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #20	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4918.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #200	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4826.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #201	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4823.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #202	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4810.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #203	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4814.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #204	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4812.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #205	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4922.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #206	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4897.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #207	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4908.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #208	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4906.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #209	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4909.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #21	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4897.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #210	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4889.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #22	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4934.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #23	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4911.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #24	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4890.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #25	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4927.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #26	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4902.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #27	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4914.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #28	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4913.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #29	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4840.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #3	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4854.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #30	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4813.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #31	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4802.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #32	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4806.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #33	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4782.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #34	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4816.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #35	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4801.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #36	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4796.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #37	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4796.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #38	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4773.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #39	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4806.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #4	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4841.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #40	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4926.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #41	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4907.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #42	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4889.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #43	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4922.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #44	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4898.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #45	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4878.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #46	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4913.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #47	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4897.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #48	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4907.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #49	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4909.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #5	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4854.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #50	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4889.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #51	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4887.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #52	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4887.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #53	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4863.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #54	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4903.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #55	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4902.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #56	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4882.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #57	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4866.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #58	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4899.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #59	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4875.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #6	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4831.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #60	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4856.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #61	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4891.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #62	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4873.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #63	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4880.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #64	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4878.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #65	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4882.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #66	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4859.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #67	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4840.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #68	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4877.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #69	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4854.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #7	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4866.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #70	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4834.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #71	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4871.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #72	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4850.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #73	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4855.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #74	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4856.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #75	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4987.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #76	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4975.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #77	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5006.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #78	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4962.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #79	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4976.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #8	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4866.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #80	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4979.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #81	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4953.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #82	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4966.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #83	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4970.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #84	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4968.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #85	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4792.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #86	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4781.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #87	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4872.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #88	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4852.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #89	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4827.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #9	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4849.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #90	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O[Si](C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4867.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #91	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4865.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #92	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4863.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #93	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4841.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #94	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4822.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #95	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4856.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #96	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	4845.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #97	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4822.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #98	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4803.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),4TMS,isomer #99	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4839.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #1	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5467.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #10	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5494.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #2	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5465.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #3	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5482.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #4	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5462.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #5	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5456.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #6	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5501.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #7	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5453.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #8	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5476.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),1TBDMS,isomer #9	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5476.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #1	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5491.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #10	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5496.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #11	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5476.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #12	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5525.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #13	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5486.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #14	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5522.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #15	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5516.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #16	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5509.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #17	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5527.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #18	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5505.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #19	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5492.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #2	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5476.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #20	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5534.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #21	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5492.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #22	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5522.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #23	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5516.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #24	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5531.7	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #25	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5481.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #26	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5551.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #27	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5507.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #28	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5503.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #29	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5498.3	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #3	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5522.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #30	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O[Si](C)(C)C(C)(C)C)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5521.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #31	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5497.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #32	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5465.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #33	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5488.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #34	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5481.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #35	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O[Si](C)(C)C(C)(C)C)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5501.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #36	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O	5528.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #37	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5533.2	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #38	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5533.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #39	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5553.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #4	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5481.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #40	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5494.6	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #41	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5492.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #42	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5513.0	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #43	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5520.9	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #44	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5528.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #45	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	5532.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #5	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5516.8	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #6	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5513.1	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #7	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5526.5	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #8	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5508.4	Semi standard non polar	33892256
Quercetin 7-(rhamnosylglucoside),2TBDMS,isomer #9	C[C@@H]1O[C@@H](O[C@H]2[C@H](OC3=CC(O)=C4C(=O)C(O)=C(C5=CC=C(O)C(O)=C5)OC4=C3)O[C@H](CO)[C@@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5525.5	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (Non-derivatized) - 70eV, Positive	splash10-0fdp-7412090000-e71b38632e054cc41028	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Quercetin 7-(rhamnosylglucoside) 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
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 10V, Positive-QTOF	splash10-0udj-0339832000-d26cc3153831e29ef1d7	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 20V, Positive-QTOF	splash10-0udi-0359400000-23e44f3911c3e7d78261	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 40V, Positive-QTOF	splash10-0udr-1957110000-97aa6a19d5bf2d9e107f	2016-06-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 10V, Negative-QTOF	splash10-0r01-3529645000-0451160270e8bbdd757e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 20V, Negative-QTOF	splash10-0w2a-2619310000-a45902315c9a741567d2	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 40V, Negative-QTOF	splash10-0udi-9737000000-499caf39cec61f49cd79	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 10V, Positive-QTOF	splash10-03di-0000009000-5c4a382bca477bf51f4a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 20V, Positive-QTOF	splash10-03di-0000009000-de6ff76c309e593f5da2	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 40V, Positive-QTOF	splash10-03di-2000913000-705b3d733ad5ea706f76	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 10V, Negative-QTOF	splash10-0a4i-0000009000-5eb189c762bf9e0d6b34	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 20V, Negative-QTOF	splash10-0a4i-0000619000-6792b7ac50995f1ebf7a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Quercetin 7-(rhamnosylglucoside) 40V, Negative-QTOF	splash10-0a4l-2500941000-43e5cbbd3ccfe32bfbb8	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	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

FDB018949

KNApSAcK ID

Not Available

Chemspider ID

4589860

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5488542

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 7-(rhamnosylglucoside) (HMDB0039383)

MOL for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

3D MOL for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

3D SDF for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

3D-SDF for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

PDB for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

3D PDB for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

SMILES for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

INCHI for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

Structure for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

3D Structure for HMDB0039383 (Quercetin 7-(rhamnosylglucoside))

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra