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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:39:38 UTC

Update Date

2022-03-07 02:55:19 UTC

HMDB ID

HMDB0037414

Secondary Accession Numbers

HMDB37414

Metabolite Identification

Common Name

8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone

Description

8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone belongs to the class of organic compounds known as flavonoid c-glycosides. Flavonoid C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone has been detected, but not quantified in, pulses and soy beans (Glycine max). This could make 8-galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone.

Structure

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


  Mrv0541 11261206162D          

 43 47  0  0  0  0            999 V2000
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 40 41  1  0  0  0  0
 16 42  1  0  0  0  0
  8 43  2  0  0  0  0
M  END

HMDB0037414
     RDKit          3D
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone
 75 79  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv0541 11261206162D          

 43 47  0  0  0  0            999 V2000
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   -6.8429   -8.4563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.5573   -7.2188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2705   -3.0937    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9850   -3.5062    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9850   -4.3312    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5561   -4.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5561   -3.5062    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6995   -4.7437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6995   -3.0937    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2705   -2.2687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8416   -3.0937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8416   -2.2687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7307   -4.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8416   -8.0438    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
  1  6  1  0  0  0  0
  7  6  1  0  0  0  0
  6  5  2  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
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  7 10  1  0  0  0  0
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  1 17  1  0  0  0  0
  3 18  1  0  0  0  0
  4 19  1  0  0  0  0
  2 20  1  0  0  0  0
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 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
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 23 30  1  1  0  0  0
 30 31  1  0  0  0  0
 34 17  1  0  0  0  0
 17 35  1  0  0  0  0
 32 33  1  0  0  0  0
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 35 36  1  0  0  0  0
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 32 39  1  1  0  0  0
 36 40  1  1  0  0  0
 40 41  1  0  0  0  0
 16 42  1  0  0  0  0
  8 43  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037414

> <DATABASE_NAME>
hmdb

> <SMILES>
COC1=C(C2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)C2=C(C(=O)C=C(O2)C2=CC=C(O)C=C2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C28H32O15/c1-40-25-16(27-23(38)21(36)18(33)13(7-29)42-27)20(35)15-11(32)6-12(9-2-4-10(31)5-3-9)41-26(15)17(25)28-24(39)22(37)19(34)14(8-30)43-28/h2-6,13-14,18-19,21-24,27-31,33-39H,7-8H2,1H3/t13-,14-,18-,19+,21+,22+,23-,24-,27?,28?/m1/s1

> <INCHI_KEY>
GHHBRJNUNAWXEV-QVCVYZROSA-N

> <FORMULA>
C28H32O15

> <MOLECULAR_WEIGHT>
608.5447

> <EXACT_MASS>
608.174120354

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
59.622614867760696

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-[(3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

> <ALOGPS_LOGP>
-0.88

> <JCHEM_LOGP>
-2.6620586203333314

> <ALOGPS_LOGS>
-2.00

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.81191079275188

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.985712032627631

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6447308947919366

> <JCHEM_POLAR_SURFACE_AREA>
256.28999999999996

> <JCHEM_REFRACTIVITY>
143.6328

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.02e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-[(3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037414
     RDKit          3D
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone
 75 79  0  0  0  0  0  0  0  0999 V2000
    1.8497   -2.4005   -1.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0712   -0.5801    0.1932 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9854    0.3374    0.6856 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3475   -0.1343    0.9356 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9680   -0.7886   -0.0972 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1042    3.3126    0.7875 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2986    2.6320   -0.0097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6865    2.8764   -0.3283 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.8099    3.8795    0.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4134    3.4598   -0.8425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7470    3.7433   -1.0955 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6384    2.7657   -1.7302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3154    2.4779   -1.4924 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6096   -2.3209    0.9513 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6804   -3.3773    1.9720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9447   -3.4742    2.5769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6488   -2.2299   -0.0835 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5884   -3.2382    0.0383 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7318   -3.6445   -1.7049 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3955   -0.2661   -2.3957 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0242   -1.6455   -1.9977 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2242   -0.9543    1.7397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0120    0.6291   -1.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7432   -0.8570   -1.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1714   -3.0943   -1.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9207   -1.0282    0.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8284    1.3332   -0.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2070    0.5479    2.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8008   -1.6413    2.9016 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
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  7 10  1  0
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 42 33  1  0
 14  5  1  0
 31 18  1  0
 29 23  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  5 47  1  0
  7 48  1  6
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 10 52  1  1
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 29 64  1  0
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 38 70  1  6
 39 71  1  0
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 41 73  1  0
 42 74  1  6
 43 75  1  0
M  END

HEADER    PROTEIN                                 26-NOV-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-NOV-12         0                                  
HETATM    1  C   UNK     0      -6.105 -10.395   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.439 -11.165   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.439 -12.705   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.105 -13.475   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.771 -12.705   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.771 -11.165   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.438 -10.395   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.438 -13.475   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.104 -12.705   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.104 -11.165   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.770 -10.395   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.563  -8.085   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.770  -8.855   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.563 -11.165   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.897 -10.395   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.897  -8.855   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.105  -8.855   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -8.772 -13.475   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.105 -15.015   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -8.772 -10.395   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0     -10.106 -11.165   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0     -10.106 -12.705   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0     -11.440 -13.475   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -11.440 -15.015   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -10.106 -15.785   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -8.772 -15.015   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -7.439 -15.785   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0     -10.106 -17.325   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0     -12.773 -15.785   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0     -12.773 -12.705   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0     -14.107 -13.475   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -6.105  -5.775   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -7.439  -6.545   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -7.439  -8.085   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -4.771  -8.085   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -4.771  -6.545   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -8.772  -8.855   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -8.772  -5.775   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      -6.105  -4.235   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -3.438  -5.775   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -3.438  -4.235   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       3.231  -8.085   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      -3.438 -15.015   0.000  0.00  0.00           O+0
CONECT    1    2    6   17                                                  
CONECT    2    1    3   20                                                  
CONECT    3    2    4   18                                                  
CONECT    4    3    5   19                                                  
CONECT    5    4    6    8                                                  
CONECT    6    1    7    5                                                  
CONECT    7    6   10                                                       
CONECT    8    5    9   43                                                  
CONECT    9    8   10                                                       
CONECT   10    9    7   11                                                  
CONECT   11   10   13   14                                                  
CONECT   12   13   16                                                       
CONECT   13   11   12                                                       
CONECT   14   11   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   12   42                                                  
CONECT   17    1   34   35                                                  
CONECT   18    3   26   22                                                  
CONECT   19    4                                                            
CONECT   20    2   21                                                       
CONECT   21   20                                                            
CONECT   22   18   23                                                       
CONECT   23   22   24   30                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26   28                                                  
CONECT   26   18   25   27                                                  
CONECT   27   26                                                            
CONECT   28   25                                                            
CONECT   29   24                                                            
CONECT   30   23   31                                                       
CONECT   31   30                                                            
CONECT   32   33   36   39                                                  
CONECT   33   32   34   38                                                  
CONECT   34   17   33   37                                                  
CONECT   35   17   36                                                       
CONECT   36   35   32   40                                                  
CONECT   37   34                                                            
CONECT   38   33                                                            
CONECT   39   32                                                            
CONECT   40   36   41                                                       
CONECT   41   40                                                            
CONECT   42   16                                                            
CONECT   43    8                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

COMPND    HMDB0037414
HETATM    1  C1  UNL     1       1.850  -2.400  -1.221  1.00  0.00           C  
HETATM    2  O1  UNL     1       1.377  -1.905  -0.002  1.00  0.00           O  
HETATM    3  C2  UNL     1       1.071  -0.580   0.193  1.00  0.00           C  
HETATM    4  C3  UNL     1       1.985   0.337   0.686  1.00  0.00           C  
HETATM    5  C4  UNL     1       3.348  -0.134   0.936  1.00  0.00           C  
HETATM    6  O2  UNL     1       3.968  -0.789  -0.097  1.00  0.00           O  
HETATM    7  C5  UNL     1       5.149  -0.290  -0.565  1.00  0.00           C  
HETATM    8  C6  UNL     1       5.731  -1.291  -1.604  1.00  0.00           C  
HETATM    9  O3  UNL     1       5.974  -2.500  -1.025  1.00  0.00           O  
HETATM   10  C7  UNL     1       6.241  -0.148   0.471  1.00  0.00           C  
HETATM   11  O4  UNL     1       7.000   1.016   0.211  1.00  0.00           O  
HETATM   12  C8  UNL     1       5.587   0.042   1.818  1.00  0.00           C  
HETATM   13  O5  UNL     1       5.174  -1.232   2.253  1.00  0.00           O  
HETATM   14  C9  UNL     1       4.298   0.852   1.512  1.00  0.00           C  
HETATM   15  O6  UNL     1       4.749   1.839   0.643  1.00  0.00           O  
HETATM   16  C10 UNL     1       1.614   1.674   0.881  1.00  0.00           C  
HETATM   17  O7  UNL     1       2.537   2.562   1.368  1.00  0.00           O  
HETATM   18  C11 UNL     1       0.319   2.019   0.562  1.00  0.00           C  
HETATM   19  C12 UNL     1      -0.104   3.313   0.787  1.00  0.00           C  
HETATM   20  O8  UNL     1       0.629   4.223   1.233  1.00  0.00           O  
HETATM   21  C13 UNL     1      -1.454   3.597   0.486  1.00  0.00           C  
HETATM   22  C14 UNL     1      -2.299   2.632  -0.010  1.00  0.00           C  
HETATM   23  C15 UNL     1      -3.686   2.876  -0.328  1.00  0.00           C  
HETATM   24  C16 UNL     1      -4.493   3.592   0.579  1.00  0.00           C  
HETATM   25  C17 UNL     1      -5.810   3.879   0.343  1.00  0.00           C  
HETATM   26  C18 UNL     1      -6.413   3.460  -0.843  1.00  0.00           C  
HETATM   27  O9  UNL     1      -7.747   3.743  -1.096  1.00  0.00           O  
HETATM   28  C19 UNL     1      -5.638   2.766  -1.730  1.00  0.00           C  
HETATM   29  C20 UNL     1      -4.315   2.478  -1.492  1.00  0.00           C  
HETATM   30  O10 UNL     1      -1.835   1.417  -0.207  1.00  0.00           O  
HETATM   31  C21 UNL     1      -0.587   1.077   0.062  1.00  0.00           C  
HETATM   32  C22 UNL     1      -0.234  -0.262  -0.142  1.00  0.00           C  
HETATM   33  C23 UNL     1      -1.233  -1.217  -0.458  1.00  0.00           C  
HETATM   34  O11 UNL     1      -1.304  -2.332   0.365  1.00  0.00           O  
HETATM   35  C24 UNL     1      -2.610  -2.321   0.951  1.00  0.00           C  
HETATM   36  C25 UNL     1      -2.680  -3.377   1.972  1.00  0.00           C  
HETATM   37  O12 UNL     1      -3.945  -3.474   2.577  1.00  0.00           O  
HETATM   38  C26 UNL     1      -3.649  -2.230  -0.083  1.00  0.00           C  
HETATM   39  O13 UNL     1      -4.588  -3.238   0.038  1.00  0.00           O  
HETATM   40  C27 UNL     1      -3.106  -2.323  -1.498  1.00  0.00           C  
HETATM   41  O14 UNL     1      -2.732  -3.645  -1.705  1.00  0.00           O  
HETATM   42  C28 UNL     1      -1.932  -1.350  -1.723  1.00  0.00           C  
HETATM   43  O15 UNL     1      -2.396  -0.266  -2.396  1.00  0.00           O  
HETATM   44  H1  UNL     1       2.024  -1.646  -1.998  1.00  0.00           H  
HETATM   45  H2  UNL     1       2.750  -3.078  -1.070  1.00  0.00           H  
HETATM   46  H3  UNL     1       1.110  -3.135  -1.698  1.00  0.00           H  
HETATM   47  H4  UNL     1       3.224  -0.954   1.740  1.00  0.00           H  
HETATM   48  H5  UNL     1       5.012   0.629  -1.192  1.00  0.00           H  
HETATM   49  H6  UNL     1       6.743  -0.857  -1.905  1.00  0.00           H  
HETATM   50  H7  UNL     1       5.133  -1.293  -2.529  1.00  0.00           H  
HETATM   51  H8  UNL     1       5.171  -3.094  -1.126  1.00  0.00           H  
HETATM   52  H9  UNL     1       6.921  -1.028   0.486  1.00  0.00           H  
HETATM   53  H10 UNL     1       6.828   1.333  -0.731  1.00  0.00           H  
HETATM   54  H11 UNL     1       6.207   0.548   2.551  1.00  0.00           H  
HETATM   55  H12 UNL     1       5.801  -1.641   2.902  1.00  0.00           H  
HETATM   56  H13 UNL     1       4.019   1.222   2.513  1.00  0.00           H  
HETATM   57  H14 UNL     1       5.376   2.417   1.081  1.00  0.00           H  
HETATM   58  H15 UNL     1       2.596   3.475   1.594  1.00  0.00           H  
HETATM   59  H16 UNL     1      -1.818   4.587   0.650  1.00  0.00           H  
HETATM   60  H17 UNL     1      -3.983   3.890   1.493  1.00  0.00           H  
HETATM   61  H18 UNL     1      -6.413   4.423   1.063  1.00  0.00           H  
HETATM   62  H19 UNL     1      -7.958   4.633  -1.576  1.00  0.00           H  
HETATM   63  H20 UNL     1      -6.115   2.436  -2.648  1.00  0.00           H  
HETATM   64  H21 UNL     1      -3.730   1.948  -2.251  1.00  0.00           H  
HETATM   65  H22 UNL     1      -2.219  -0.580   0.106  1.00  0.00           H  
HETATM   66  H23 UNL     1      -2.653  -1.326   1.527  1.00  0.00           H  
HETATM   67  H24 UNL     1      -2.390  -4.382   1.640  1.00  0.00           H  
HETATM   68  H25 UNL     1      -1.977  -3.148   2.846  1.00  0.00           H  
HETATM   69  H26 UNL     1      -3.871  -3.803   3.487  1.00  0.00           H  
HETATM   70  H27 UNL     1      -4.254  -1.275  -0.001  1.00  0.00           H  
HETATM   71  H28 UNL     1      -4.895  -3.621  -0.825  1.00  0.00           H  
HETATM   72  H29 UNL     1      -3.956  -2.112  -2.183  1.00  0.00           H  
HETATM   73  H30 UNL     1      -2.864  -4.201  -0.870  1.00  0.00           H  
HETATM   74  H31 UNL     1      -1.234  -1.986  -2.398  1.00  0.00           H  
HETATM   75  H32 UNL     1      -2.397  -0.469  -3.385  1.00  0.00           H  
CONECT    1    2   44   45   46
CONECT    2    3
CONECT    3    4    4   32
CONECT    4    5   16
CONECT    5    6   14   47
CONECT    6    7
CONECT    7    8   10   48
CONECT    8    9   49   50
CONECT    9   51
CONECT   10   11   12   52
CONECT   11   53
CONECT   12   13   14   54
CONECT   13   55
CONECT   14   15   56
CONECT   15   57
CONECT   16   17   18   18
CONECT   17   58
CONECT   18   19   31
CONECT   19   20   20   21
CONECT   21   22   22   59
CONECT   22   23   30
CONECT   23   24   24   29
CONECT   24   25   60
CONECT   25   26   26   61
CONECT   26   27   28
CONECT   27   62
CONECT   28   29   29   63
CONECT   29   64
CONECT   30   31
CONECT   31   32   32
CONECT   32   33
CONECT   33   34   42   65
CONECT   34   35
CONECT   35   36   38   66
CONECT   36   37   67   68
CONECT   37   69
CONECT   38   39   40   70
CONECT   39   71
CONECT   40   41   42   72
CONECT   41   73
CONECT   42   43   74
CONECT   43   75
END

HMDB0037414
     RDKit          3D
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone
 75 79  0  0  0  0  0  0  0  0999 V2000
    1.8497   -2.4005   -1.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3770   -1.9049   -0.0019 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0712   -0.5801    0.1932 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9854    0.3374    0.6856 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3475   -0.1343    0.9356 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9680   -0.7886   -0.0972 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1487   -0.2899   -0.5647 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7313   -1.2911   -1.6045 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9741   -2.5001   -1.0250 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2412   -0.1480    0.4713 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0002    1.0162    0.2113 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5868    0.0423    1.8178 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1739   -1.2322    2.2532 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2977    0.8523    1.5123 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7494    1.8391    0.6433 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6141    1.6744    0.8813 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5371    2.5618    1.3679 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3186    2.0187    0.5625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1042    3.3126    0.7875 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6290    4.2230    1.2327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4536    3.5968    0.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2986    2.6320   -0.0097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6865    2.8764   -0.3283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4931    3.5920    0.5792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8099    3.8795    0.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4134    3.4598   -0.8425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7470    3.7433   -1.0955 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6384    2.7657   -1.7302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3154    2.4779   -1.4924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8348    1.4171   -0.2070 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5875    1.0775    0.0625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2340   -0.2619   -0.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2326   -1.2174   -0.4582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3043   -2.3318    0.3652 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6096   -2.3209    0.9513 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6804   -3.3773    1.9720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9447   -3.4742    2.5769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6488   -2.2299   -0.0835 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5884   -3.2382    0.0383 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1056   -2.3232   -1.4979 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7318   -3.6445   -1.7049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9323   -1.3501   -1.7227 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3955   -0.2661   -2.3957 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0242   -1.6455   -1.9977 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7497   -3.0781   -1.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1101   -3.1355   -1.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2242   -0.9543    1.7397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0120    0.6291   -1.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7432   -0.8570   -1.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1325   -1.2932   -2.5285 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1714   -3.0943   -1.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9207   -1.0282    0.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8284    1.3332   -0.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2070    0.5479    2.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8008   -1.6413    2.9016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0186    1.2217    2.5131 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3758    2.4173    1.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5959    3.4754    1.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8177    4.5871    0.6501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9829    3.8896    1.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4134    4.4228    1.0628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9580    4.6326   -1.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1147    2.4363   -2.6482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7296    1.9484   -2.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2190   -0.5798    0.1062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6525   -1.3265    1.5269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3896   -4.3820    1.6403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9769   -3.1480    2.8463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8707   -3.8035    3.4868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2537   -1.2748   -0.0006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8951   -3.6212   -0.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9561   -2.1124   -2.1833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8642   -4.2009   -0.8703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2338   -1.9863   -2.3977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3966   -0.4693   -3.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  4 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26 28  1  0
 28 29  2  0
 22 30  1  0
 30 31  1  0
 31 32  2  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 35 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 32  3  1  0
 42 33  1  0
 14  5  1  0
 31 18  1  0
 29 23  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  5 47  1  0
  7 48  1  6
  8 49  1  0
  8 50  1  0
  9 51  1  0
 10 52  1  1
 11 53  1  0
 12 54  1  1
 13 55  1  0
 14 56  1  1
 15 57  1  0
 17 58  1  0
 21 59  1  0
 24 60  1  0
 25 61  1  0
 27 62  1  0
 28 63  1  0
 29 64  1  0
 33 65  1  0
 35 66  1  1
 36 67  1  0
 36 68  1  0
 37 69  1  0
 38 70  1  6
 39 71  1  0
 40 72  1  6
 41 73  1  0
 42 74  1  6
 43 75  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
8-Galactopyranosyl-6-glucopyranosylgenkwanin	HMDB
8-Galactosyl-6-glucosylgenkwanin	HMDB

Chemical Formula

C₂₈H₃₂O₁₅

Average Molecular Weight

608.5447

Monoisotopic Molecular Weight

608.174120354

IUPAC Name

5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-[(3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

Traditional Name

5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-[(3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

CAS Registry Number

Not Available

SMILES

COC1=C(C2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)C2=C(C(=O)C=C(O2)C2=CC=C(O)C=C2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C28H32O15/c1-40-25-16(27-23(38)21(36)18(33)13(7-29)42-27)20(35)15-11(32)6-12(9-2-4-10(31)5-3-9)41-26(15)17(25)28-24(39)22(37)19(34)14(8-30)43-28/h2-6,13-14,18-19,21-24,27-31,33-39H,7-8H2,1H3/t13-,14-,18-,19+,21+,22+,23-,24-,27?,28?/m1/s1

InChI Key

GHHBRJNUNAWXEV-QVCVYZROSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid C-glycosides

Alternative Parents

Substituents

Flavonoid c-glycoside
4p-methoxyflavonoid-skeleton
Hydroxyflavonoid
Flavone
5-hydroxyflavonoid
7-hydroxyflavonoid
Phenolic glycoside
Hexose monosaccharide
C-glycosyl compound
Chromone
Glycosyl compound
Benzopyran
1-benzopyran
Anisole
Methoxybenzene
Phenol ether
Phenoxy compound
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Monocyclic benzene moiety
Benzenoid
Pyran
Oxane
Monosaccharide
Vinylogous acid
Heteroaromatic compound
Secondary alcohol
Ether
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Polyol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Primary alcohol
Alcohol
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0037414)
Cytoplasm (HMDB: HMDB0037414)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037414)

Source

Exogenous

Food

Food (HMDB: HMDB0037414)

Soy

Soy bean (FooDB: FOOD00085)

Pulse

Pulses (FooDB: FOOD00867)

Not Available

Nutrient (HMDB: HMDB0037414)

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	6.02 g/L	ALOGPS
logP	-0.88	ALOGPS
logP	-2.7	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	7.99	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	256.29 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	143.63 m³·mol⁻¹	ChemAxon
Polarizability	59.62 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]+	220.551	30932474
DeepCCS	[M-H]-	218.521	30932474
DeepCCS	[M-2H]-	252.553	30932474
DeepCCS	[M+Na]+	226.832	30932474
AllCCS	[M+H]+	236.5	32859911
AllCCS	[M+H-H2O]+	235.1	32859911
AllCCS	[M+NH4]+	237.7	32859911
AllCCS	[M+Na]+	238.0	32859911
AllCCS	[M-H]-	237.2	32859911
AllCCS	[M+Na-2H]-	239.8	32859911
AllCCS	[M+HCOO]-	242.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone	COC1=C(C2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)C2=C(C(=O)C=C(O2)C2=CC=C(O)C=C2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	5139.0	Standard polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone	COC1=C(C2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)C2=C(C(=O)C=C(O2)C2=CC=C(O)C=C2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	4975.2	Standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone	COC1=C(C2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)C2=C(C(=O)C=C(O2)C2=CC=C(O)C=C2)C(O)=C1C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	5695.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #1	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5340.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #10	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5416.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #2	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5367.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #3	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5372.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #4	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5413.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #5	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5447.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #6	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5378.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #7	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5339.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #8	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5368.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TMS,isomer #9	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5374.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #1	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5168.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #10	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5172.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #11	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5182.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #12	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5182.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #13	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5205.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #14	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5190.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #15	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5218.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #16	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5203.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #17	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5217.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #18	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5165.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #19	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5179.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #2	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5172.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #20	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5182.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #21	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5203.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #22	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5175.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #23	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5212.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #24	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5224.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #25	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5191.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #26	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5202.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #27	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5203.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #28	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5236.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #29	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5195.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #3	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5167.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #30	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5234.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #31	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5212.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #32	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5219.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #33	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5215.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #34	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5242.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #35	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5229.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #36	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5173.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #37	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5194.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #38	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5181.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #39	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5204.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #4	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5194.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #40	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5193.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #41	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5176.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #42	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5207.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #43	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5206.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #44	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5222.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #45	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5232.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #5	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5169.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #6	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5212.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #7	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5193.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #8	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5173.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TMS,isomer #9	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5201.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #1	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5037.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #10	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5058.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #100	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5072.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #101	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5088.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #102	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5063.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #103	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5111.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #104	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5054.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #105	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5071.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #106	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5099.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #107	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5063.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #108	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5097.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #109	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5051.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #11	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5011.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #110	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5079.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #111	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5020.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #112	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4990.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #113	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5037.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #114	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5008.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #115	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5037.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #116	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5031.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #117	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5044.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #118	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5074.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #119	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5061.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #12	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5074.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #120	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5084.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #13	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5033.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #14	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5011.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #15	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5054.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #16	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5055.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #17	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4990.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #18	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5059.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #19	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5021.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #2	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5015.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #20	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5001.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #21	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5044.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #22	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5027.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #23	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5098.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #24	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5065.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #25	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5041.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #26	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5085.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #27	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5054.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #28	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5021.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #29	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4991.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #3	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5064.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #30	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5034.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #31	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5086.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #32	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5060.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #33	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5103.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #34	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5043.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #35	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5067.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #36	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5053.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #37	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5033.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #38	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5012.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #39	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5061.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #4	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5009.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #40	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5012.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #41	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5074.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #42	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5028.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #43	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5052.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #44	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5030.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #45	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5058.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #46	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5020.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #47	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5070.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #48	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5029.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #49	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5052.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #5	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5074.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #50	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5056.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #51	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5003.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #52	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5055.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #53	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5019.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #54	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5040.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #55	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5035.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #56	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5093.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #57	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5058.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #58	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5079.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #59	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5060.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #6	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	5038.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #60	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5010.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #61	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5035.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #62	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	5069.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #63	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	5092.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #64	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5078.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #65	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5020.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #66	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5001.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #67	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5049.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #68	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4990.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #69	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5058.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #7	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5015.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #70	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5050.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #71	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5019.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #72	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5044.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #73	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5000.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #74	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5053.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #75	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5051.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #76	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5043.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #77	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4983.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #78	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5045.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #79	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5040.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #8	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5058.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #80	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5015.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #81	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5074.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #82	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5078.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #83	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	5048.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #84	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5026.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #85	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	5089.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #86	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5060.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #87	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5036.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #88	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5087.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #89	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5024.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #9	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5028.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #90	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5094.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #91	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5053.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #92	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5080.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #93	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5031.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #94	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5090.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #95	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5080.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #96	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5012.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #97	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5072.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #98	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5045.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,3TMS,isomer #99	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	5113.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #1	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4922.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #10	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4922.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #100	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4915.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #101	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4874.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #102	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4888.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #103	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4937.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #104	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4952.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #105	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4953.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #106	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4953.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #107	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4859.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #108	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4926.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #109	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4899.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #11	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4894.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #110	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4916.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #111	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4878.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #112	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4946.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #113	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4922.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #114	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4934.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #115	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4910.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #116	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4859.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #117	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4873.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #118	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4925.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #119	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4940.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #12	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4852.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #120	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4949.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #121	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4873.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #122	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4944.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #123	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4916.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #124	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4931.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #125	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4896.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #126	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4829.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #127	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4843.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #128	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4906.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #129	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4922.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #13	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4910.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #130	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4919.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #131	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4923.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #132	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4870.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #133	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4885.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #134	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4941.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #135	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4955.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #136	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4966.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #137	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4904.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #138	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4923.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #139	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4900.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #14	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4910.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #140	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4967.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #141	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4888.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #142	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4912.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #143	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4851.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #144	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4925.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #145	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4932.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #146	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4893.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #147	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4817.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #148	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4895.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #149	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4894.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #15	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4973.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #150	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4867.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #151	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4944.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #152	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4949.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #153	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4892.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #154	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4885.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #155	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4951.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #156	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4923.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #157	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4827.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #158	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4906.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #159	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4913.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #16	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4952.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #160	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4846.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #161	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4927.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #162	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4933.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #163	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4894.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #164	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4870.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #165	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4939.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #166	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4841.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #167	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4926.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #168	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4930.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #169	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4889.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #17	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4915.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #170	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4839.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #171	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4922.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #172	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4910.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #173	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4881.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #174	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4957.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #175	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4919.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #176	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4934.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #177	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4957.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #178	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4893.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #179	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4963.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #18	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4963.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #180	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4939.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #181	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4855.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #182	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4930.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #183	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4908.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #184	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4979.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #185	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4926.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #186	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4966.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #187	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4866.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #188	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4936.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #189	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4885.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #19	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4924.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #190	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4957.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #191	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4920.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #192	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4882.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #193	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4956.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #194	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4907.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #195	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4936.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #196	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4949.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #197	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4973.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #198	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4917.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #199	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4955.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #2	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4945.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #20	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4897.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #200	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4895.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #201	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4938.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #202	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4973.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #203	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4902.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #204	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4924.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #205	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4921.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #206	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4884.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #207	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4897.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #208	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4885.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #209	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4901.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #21	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4859.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #210	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	4972.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #22	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4907.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #23	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4956.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #24	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4922.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #25	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4966.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #26	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4925.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #27	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4941.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #28	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4930.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #29	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4956.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #3	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4896.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #30	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4872.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #31	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4936.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #32	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4917.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #33	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4876.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #34	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4931.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #35	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4890.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #36	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4959.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #37	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4939.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #38	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4898.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #39	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4951.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #4	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4955.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #40	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4913.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #41	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4885.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #42	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4849.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #43	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4896.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #44	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4951.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #45	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4917.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #46	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4961.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #47	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4918.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #48	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4936.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #49	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4922.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #5	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4932.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #50	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4887.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #51	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4956.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #52	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4934.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #53	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4895.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #54	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4947.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #55	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4891.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #56	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4853.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #57	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4819.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #58	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4864.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #59	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4925.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #6	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4893.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #60	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4895.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #61	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4936.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #62	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4890.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #63	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4906.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #64	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4891.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #65	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4926.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #66	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4897.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #67	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4860.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #68	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4908.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #69	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4969.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #7	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4947.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #70	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4936.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #71	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4977.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #72	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4939.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #73	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4956.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #74	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4939.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #75	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4921.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #76	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	4897.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #77	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	4937.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #78	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4887.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #79	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4897.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #8	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4931.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #80	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4883.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #81	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4950.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #82	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4964.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #83	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4948.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #84	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[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	4967.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #85	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4917.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #86	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4942.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #87	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4885.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #88	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4951.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #89	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4917.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #9	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]1O	4859.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #90	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4933.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #91	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4924.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #92	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4850.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #93	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4917.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #94	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4875.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #95	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4894.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #96	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4901.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #97	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	4969.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #98	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4937.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,4TMS,isomer #99	COC1=C(C2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4952.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #1	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5540.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #10	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5580.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #2	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5551.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #3	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5548.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #4	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5578.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #5	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5620.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #6	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5582.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #7	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5539.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #8	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5551.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,1TBDMS,isomer #9	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5550.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #1	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5528.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #10	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5538.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #11	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5547.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #12	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5545.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #13	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5556.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #14	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5571.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #15	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5599.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #16	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5543.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #17	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5558.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #18	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5534.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #19	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5545.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #2	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5539.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #20	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5546.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #21	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5551.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #22	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5575.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #23	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5604.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #24	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	5552.0	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #25	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5541.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #26	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5552.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #27	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5547.3	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #28	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5562.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #29	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5581.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #3	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5535.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #30	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5608.4	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #31	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5588.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #32	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5601.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #33	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5606.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #34	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5614.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #35	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5651.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #36	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5559.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #37	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5571.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #38	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5578.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #39	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5585.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #4	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5545.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #40	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5547.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #41	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5531.8	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #42	COC1=C(C2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5562.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #43	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5546.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #44	COC1=C(C2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5562.6	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #45	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O	5558.5	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #5	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5558.9	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #6	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O	5587.1	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #7	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	5546.2	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #8	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	5529.7	Semi standard non polar	33892256
8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone,2TBDMS,isomer #9	COC1=C(C2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(O)=C2C(=O)C=C(C3=CC=C(O)C=C3)OC2=C1C1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	5557.1	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (Non-derivatized) - 70eV, Positive	splash10-016v-0000290000-7d453993708da745bd8f	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 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 - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 10V, Positive-QTOF	splash10-0a4l-0000296000-620b3548b0e1a120112b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 20V, Positive-QTOF	splash10-0596-1200391000-81c6edb93c20e6bf4969	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 40V, Positive-QTOF	splash10-0072-1006950000-243b24d571687ce509f5	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 10V, Negative-QTOF	splash10-0a4i-1000589000-7a1cf10adce71a267959	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 20V, Negative-QTOF	splash10-059i-4001591000-1bf5e0e8bfb41420a654	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 40V, Negative-QTOF	splash10-1003-6305890000-d83b91d74f8d9dd86908	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 10V, Positive-QTOF	splash10-0a4i-0000009000-5173fa625817f68f2d64	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 20V, Positive-QTOF	splash10-0a4i-0000019000-8ecb6709b0b7df46bd54	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 40V, Positive-QTOF	splash10-0uxu-0300490000-390025c112671980b627	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 10V, Negative-QTOF	splash10-0a4i-0000009000-e09c25ab08f2465d6f8b	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 20V, Negative-QTOF	splash10-0btc-0000097000-6405f1e9378dac5124aa	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB016460

KNApSAcK ID

Not Available

Chemspider ID

35014418

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131752186

PDB ID

Not Available

ChEBI ID

176218

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 8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone (HMDB0037414)

MOL for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

3D MOL for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

3D SDF for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

3D-SDF for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

PDB for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

3D PDB for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

SMILES for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

INCHI for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

Structure for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

3D Structure for HMDB0037414 (8-Galactopyranosyl-6-glucopyranosyl-4',5-dihydroxy-7-methoxyflavone)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra