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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-12 03:33:32 UTC

Update Date

2022-03-07 02:57:06 UTC

HMDB ID

HMDB0041640

Secondary Accession Numbers

HMDB41640

Metabolite Identification

Common Name

(-)-Epigallocatechin 7-glucuronide

Description

(-)-Epigallocatechin 7-glucuronide belongs to the class of organic compounds known as flavonoid-7-o-glucuronides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to glucuronic acid at the C7-position. Based on a literature review very few articles have been published on (-)-Epigallocatechin 7-glucuronide.

Structure

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


  Mrv0541 02271201272D          

 34 37  0  0  1  0            999 V2000
   -0.8826   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5971   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3115   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3115   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5971    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8826   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1681    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5464   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2608    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9753   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2608    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9753    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5464    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5464    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1681    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7405   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4549    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7405   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1681   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8839    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1694    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1694    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8839    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4549    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7405    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7405    2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4549    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4549    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3115    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  7 15  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
  1 22  1  6  0  0  0
 27 18  1  1  0  0  0
 24 23  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  6  0  0  0
 29 32  1  1  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
M  END

HMDB0041640
     RDKit          3D
(-)-Epigallocatechin 7-glucuronide
 56 59  0  0  0  0  0  0  0  0999 V2000
   -4.4990    0.9689    2.7644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3901    0.5621    1.9792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4617   -0.1240    2.5107 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2605    0.8283    0.5415 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1109    1.5223    0.2938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1590    0.8280   -0.4665 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6560   -0.2650    0.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693   -0.4495    0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0073   -1.6350    1.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2828   -1.8525    1.7001 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5970   -3.0489    2.3757 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2619   -0.9214    1.4637 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9444    0.2245    0.8115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3720    0.4595    0.3812 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8751    1.2160    0.5324 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1974    1.0988    0.9435 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0419    0.7748   -0.2523 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2260    1.4577   -0.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0408    1.2001   -1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2357    1.8907   -1.6679 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6460    0.2356   -2.4218 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4411   -0.0502   -3.5215 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4563   -0.4356   -2.2333 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0686   -1.3994   -3.1600 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6265   -0.1816   -1.1442 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    0.1144    2.0313 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8004   -0.2378    1.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6530   -1.1493    1.9111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7272    0.4730   -1.8336 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7111    1.6381   -2.5995 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1406   -0.0290   -1.7363 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3231   -1.1339   -2.5683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4080   -0.4198   -0.2990 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.7226   -0.8722   -0.1795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2450    0.3057    2.9891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1477    1.4723    0.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3691    1.5663   -0.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7807   -2.3462    1.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5272   -3.2608    2.6985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5610    1.4078   -0.1406 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4995    2.1092    1.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4954    2.2087    0.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5034    2.5795   -0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3128    0.4393   -3.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6190   -1.6231   -3.9554 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7031   -0.7353   -1.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818    0.5526    3.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1425   -0.4679    2.8894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1961   -1.8727    1.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6614   -1.6142    2.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -0.2509   -2.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6009    2.0803   -2.6162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8713    0.7950   -1.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2502   -1.9395   -1.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7632   -1.2462    0.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8288   -1.4476    0.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 16 26  1  0
 26 27  1  0
 26 28  1  0
  6 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33  4  1  0
 14  8  1  0
 25 17  1  0
 28 12  1  0
  3 35  1  0
  4 36  1  6
  6 37  1  6
  9 38  1  0
 11 39  1  0
 14 40  1  0
 16 41  1  1
 18 42  1  0
 20 43  1  0
 22 44  1  0
 24 45  1  0
 25 46  1  0
 26 47  1  1
 27 48  1  0
 28 49  1  0
 28 50  1  0
 29 51  1  6
 30 52  1  0
 31 53  1  6
 32 54  1  0
 33 55  1  1
 34 56  1  0
M  END


  Mrv0541 02271201272D          

 34 37  0  0  1  0            999 V2000
   -0.8826   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5971   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3115   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3115   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5971    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8826   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1681    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5464   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2608    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9753   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2608    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9753    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5464    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5464    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1681    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7405   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4549    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7405   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1681   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8839    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1694    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1694    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8839    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4549    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7405    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7405    2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4549    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4549    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3115    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  7 15  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
  1 22  1  6  0  0  0
 27 18  1  1  0  0  0
 24 23  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  6  0  0  0
 29 32  1  1  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0041640

> <DATABASE_NAME>
hmdb

> <SMILES>
O[C@@H]1CC2=C(O[C@@H]1C1=CC(O)=C(O)C(O)=C1)C=C(O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)C=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O13/c22-9-3-7(32-21-17(29)15(27)16(28)19(34-21)20(30)31)4-13-8(9)5-12(25)18(33-13)6-1-10(23)14(26)11(24)2-6/h1-4,12,15-19,21-29H,5H2,(H,30,31)/t12-,15+,16+,17-,18-,19+,21-/m1/s1

> <INCHI_KEY>
DMDNCGKEYCRXOR-CVPXIJHMSA-N

> <FORMULA>
C21H22O13

> <MOLECULAR_WEIGHT>
482.3916

> <EXACT_MASS>
482.10604079

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_AVERAGE_POLARIZABILITY>
45.326588216081745

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4S,5R,6S)-6-{[(2R,3R)-3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

> <ALOGPS_LOGP>
0.37

> <JCHEM_LOGP>
-0.4562518616666663

> <ALOGPS_LOGS>
-2.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.747536377474951

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8439211529107116

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7319986498042974

> <JCHEM_POLAR_SURFACE_AREA>
226.82999999999996

> <JCHEM_REFRACTIVITY>
107.99239999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.07e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4S,5R,6S)-6-{[(2R,3R)-3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0041640
     RDKit          3D
(-)-Epigallocatechin 7-glucuronide
 56 59  0  0  0  0  0  0  0  0999 V2000
   -4.4990    0.9689    2.7644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3901    0.5621    1.9792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4617   -0.1240    2.5107 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2605    0.8283    0.5415 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1109    1.5223    0.2938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1590    0.8280   -0.4665 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6560   -0.2650    0.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693   -0.4495    0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0073   -1.6350    1.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2828   -1.8525    1.7001 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5970   -3.0489    2.3757 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2619   -0.9214    1.4637 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9444    0.2245    0.8115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3720    0.4595    0.3812 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8751    1.2160    0.5324 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1974    1.0988    0.9435 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0419    0.7748   -0.2523 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2260    1.4577   -0.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0408    1.2001   -1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2357    1.8907   -1.6679 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6460    0.2356   -2.4218 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4411   -0.0502   -3.5215 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4563   -0.4356   -2.2333 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0686   -1.3994   -3.1600 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6265   -0.1816   -1.1442 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    0.1144    2.0313 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8004   -0.2378    1.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6530   -1.1493    1.9111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7272    0.4730   -1.8336 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7111    1.6381   -2.5995 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1406   -0.0290   -1.7363 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3231   -1.1339   -2.5683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4080   -0.4198   -0.2990 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.7226   -0.8722   -0.1795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2450    0.3057    2.9891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1477    1.4723    0.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3691    1.5663   -0.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7807   -2.3462    1.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5272   -3.2608    2.6985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5610    1.4078   -0.1406 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4995    2.1092    1.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4954    2.2087    0.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5034    2.5795   -0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3128    0.4393   -3.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6190   -1.6231   -3.9554 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7031   -0.7353   -1.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818    0.5526    3.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1425   -0.4679    2.8894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1961   -1.8727    1.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6614   -1.6142    2.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -0.2509   -2.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6009    2.0803   -2.6162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8713    0.7950   -1.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2502   -1.9395   -1.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7632   -1.2462    0.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8288   -1.4476    0.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 16 26  1  0
 26 27  1  0
 26 28  1  0
  6 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33  4  1  0
 14  8  1  0
 25 17  1  0
 28 12  1  0
  3 35  1  0
  4 36  1  6
  6 37  1  6
  9 38  1  0
 11 39  1  0
 14 40  1  0
 16 41  1  1
 18 42  1  0
 20 43  1  0
 22 44  1  0
 24 45  1  0
 25 46  1  0
 26 47  1  1
 27 48  1  0
 28 49  1  0
 28 50  1  0
 29 51  1  6
 30 52  1  0
 31 53  1  6
 32 54  1  0
 33 55  1  1
 34 56  1  0
M  END

HEADER    PROTEIN                                 27-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-FEB-12         0                                  
HETATM    1  C   UNK     0      -1.648  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.981  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.315  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.315  -0.770   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.981   0.000   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.648  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.314   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.020  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.353   0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.687  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.353   1.540   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.687   2.310   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.020   2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.020   3.850   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.314   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.649   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.982  -0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -8.316   0.000   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -6.982  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.649  -3.080   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -5.649  -4.620   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -0.314  -3.080   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0     -10.983   4.620   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -9.650   3.850   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -9.650   2.310   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0     -10.983   1.540   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -8.316   1.540   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.982   2.310   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -6.982   3.850   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.316   4.620   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -8.316   6.160   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -5.649   4.620   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -5.649   6.160   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -4.315   3.850   0.000  0.00  0.00           O+0
CONECT    1    2    6   22                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8   15                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    7                                                       
CONECT   16    4   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17   27                                                       
CONECT   19   17   20                                                       
CONECT   20   19    3   21                                                  
CONECT   21   20                                                            
CONECT   22    1                                                            
CONECT   23   24                                                            
CONECT   24   23   25   30                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   18   25   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   32                                                  
CONECT   30   29   24   31                                                  
CONECT   31   30                                                            
CONECT   32   29   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

COMPND    HMDB0041640
HETATM    1  O1  UNL     1      -4.499   0.969   2.764  1.00  0.00           O  
HETATM    2  C1  UNL     1      -5.390   0.562   1.979  1.00  0.00           C  
HETATM    3  O2  UNL     1      -6.462  -0.124   2.511  1.00  0.00           O  
HETATM    4  C2  UNL     1      -5.261   0.828   0.542  1.00  0.00           C  
HETATM    5  O3  UNL     1      -4.111   1.522   0.294  1.00  0.00           O  
HETATM    6  C3  UNL     1      -3.159   0.828  -0.467  1.00  0.00           C  
HETATM    7  O4  UNL     1      -2.656  -0.265   0.205  1.00  0.00           O  
HETATM    8  C4  UNL     1      -1.369  -0.450   0.603  1.00  0.00           C  
HETATM    9  C5  UNL     1      -1.007  -1.635   1.285  1.00  0.00           C  
HETATM   10  C6  UNL     1       0.283  -1.853   1.700  1.00  0.00           C  
HETATM   11  O5  UNL     1       0.597  -3.049   2.376  1.00  0.00           O  
HETATM   12  C7  UNL     1       1.262  -0.921   1.464  1.00  0.00           C  
HETATM   13  C8  UNL     1       0.944   0.224   0.812  1.00  0.00           C  
HETATM   14  C9  UNL     1      -0.372   0.460   0.381  1.00  0.00           C  
HETATM   15  O6  UNL     1       1.875   1.216   0.532  1.00  0.00           O  
HETATM   16  C10 UNL     1       3.197   1.099   0.944  1.00  0.00           C  
HETATM   17  C11 UNL     1       4.042   0.775  -0.252  1.00  0.00           C  
HETATM   18  C12 UNL     1       5.226   1.458  -0.420  1.00  0.00           C  
HETATM   19  C13 UNL     1       6.041   1.200  -1.500  1.00  0.00           C  
HETATM   20  O7  UNL     1       7.236   1.891  -1.668  1.00  0.00           O  
HETATM   21  C14 UNL     1       5.646   0.236  -2.422  1.00  0.00           C  
HETATM   22  O8  UNL     1       6.441  -0.050  -3.521  1.00  0.00           O  
HETATM   23  C15 UNL     1       4.456  -0.436  -2.233  1.00  0.00           C  
HETATM   24  O9  UNL     1       4.069  -1.399  -3.160  1.00  0.00           O  
HETATM   25  C16 UNL     1       3.627  -0.182  -1.144  1.00  0.00           C  
HETATM   26  C17 UNL     1       3.431   0.114   2.031  1.00  0.00           C  
HETATM   27  O10 UNL     1       4.800  -0.238   1.987  1.00  0.00           O  
HETATM   28  C18 UNL     1       2.653  -1.149   1.911  1.00  0.00           C  
HETATM   29  C19 UNL     1      -3.727   0.473  -1.834  1.00  0.00           C  
HETATM   30  O11 UNL     1      -3.711   1.638  -2.599  1.00  0.00           O  
HETATM   31  C20 UNL     1      -5.141  -0.029  -1.736  1.00  0.00           C  
HETATM   32  O12 UNL     1      -5.323  -1.134  -2.568  1.00  0.00           O  
HETATM   33  C21 UNL     1      -5.408  -0.420  -0.299  1.00  0.00           C  
HETATM   34  O13 UNL     1      -6.723  -0.872  -0.179  1.00  0.00           O  
HETATM   35  H1  UNL     1      -7.245   0.306   2.989  1.00  0.00           H  
HETATM   36  H2  UNL     1      -6.148   1.472   0.267  1.00  0.00           H  
HETATM   37  H3  UNL     1      -2.369   1.566  -0.667  1.00  0.00           H  
HETATM   38  H4  UNL     1      -1.781  -2.346   1.459  1.00  0.00           H  
HETATM   39  H5  UNL     1       1.527  -3.261   2.699  1.00  0.00           H  
HETATM   40  H6  UNL     1      -0.561   1.408  -0.141  1.00  0.00           H  
HETATM   41  H7  UNL     1       3.499   2.109   1.346  1.00  0.00           H  
HETATM   42  H8  UNL     1       5.495   2.209   0.332  1.00  0.00           H  
HETATM   43  H9  UNL     1       7.503   2.579  -0.997  1.00  0.00           H  
HETATM   44  H10 UNL     1       7.313   0.439  -3.663  1.00  0.00           H  
HETATM   45  H11 UNL     1       4.619  -1.623  -3.955  1.00  0.00           H  
HETATM   46  H12 UNL     1       2.703  -0.735  -1.042  1.00  0.00           H  
HETATM   47  H13 UNL     1       3.282   0.553   3.045  1.00  0.00           H  
HETATM   48  H14 UNL     1       5.142  -0.468   2.889  1.00  0.00           H  
HETATM   49  H15 UNL     1       3.196  -1.873   1.263  1.00  0.00           H  
HETATM   50  H16 UNL     1       2.661  -1.614   2.943  1.00  0.00           H  
HETATM   51  H17 UNL     1      -3.032  -0.251  -2.289  1.00  0.00           H  
HETATM   52  H18 UNL     1      -4.601   2.080  -2.616  1.00  0.00           H  
HETATM   53  H19 UNL     1      -5.871   0.795  -1.983  1.00  0.00           H  
HETATM   54  H20 UNL     1      -5.250  -1.939  -1.997  1.00  0.00           H  
HETATM   55  H21 UNL     1      -4.763  -1.246   0.019  1.00  0.00           H  
HETATM   56  H22 UNL     1      -6.829  -1.448   0.618  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   35
CONECT    4    5   33   36
CONECT    5    6
CONECT    6    7   29   37
CONECT    7    8
CONECT    8    9    9   14
CONECT    9   10   38
CONECT   10   11   12   12
CONECT   11   39
CONECT   12   13   28
CONECT   13   14   14   15
CONECT   14   40
CONECT   15   16
CONECT   16   17   26   41
CONECT   17   18   18   25
CONECT   18   19   42
CONECT   19   20   21   21
CONECT   20   43
CONECT   21   22   23
CONECT   22   44
CONECT   23   24   25   25
CONECT   24   45
CONECT   25   46
CONECT   26   27   28   47
CONECT   27   48
CONECT   28   49   50
CONECT   29   30   31   51
CONECT   30   52
CONECT   31   32   33   53
CONECT   32   54
CONECT   33   34   55
CONECT   34   56
END

HMDB0041640
     RDKit          3D
(-)-Epigallocatechin 7-glucuronide
 56 59  0  0  0  0  0  0  0  0999 V2000
   -4.4990    0.9689    2.7644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3901    0.5621    1.9792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4617   -0.1240    2.5107 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2605    0.8283    0.5415 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1109    1.5223    0.2938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1590    0.8280   -0.4665 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6560   -0.2650    0.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693   -0.4495    0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0073   -1.6350    1.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2828   -1.8525    1.7001 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5970   -3.0489    2.3757 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2619   -0.9214    1.4637 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9444    0.2245    0.8115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3720    0.4595    0.3812 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8751    1.2160    0.5324 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1974    1.0988    0.9435 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0419    0.7748   -0.2523 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2260    1.4577   -0.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0408    1.2001   -1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2357    1.8907   -1.6679 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6460    0.2356   -2.4218 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4411   -0.0502   -3.5215 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4563   -0.4356   -2.2333 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0686   -1.3994   -3.1600 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6265   -0.1816   -1.1442 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    0.1144    2.0313 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8004   -0.2378    1.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6530   -1.1493    1.9111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7272    0.4730   -1.8336 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7111    1.6381   -2.5995 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1406   -0.0290   -1.7363 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3231   -1.1339   -2.5683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4080   -0.4198   -0.2990 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.7226   -0.8722   -0.1795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2450    0.3057    2.9891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1477    1.4723    0.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3691    1.5663   -0.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7807   -2.3462    1.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5272   -3.2608    2.6985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5610    1.4078   -0.1406 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4995    2.1092    1.3464 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4954    2.2087    0.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5034    2.5795   -0.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3128    0.4393   -3.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6190   -1.6231   -3.9554 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7031   -0.7353   -1.0417 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818    0.5526    3.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1425   -0.4679    2.8894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1961   -1.8727    1.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6614   -1.6142    2.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -0.2509   -2.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6009    2.0803   -2.6162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8713    0.7950   -1.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2502   -1.9395   -1.9971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7632   -1.2462    0.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8288   -1.4476    0.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 16 26  1  0
 26 27  1  0
 26 28  1  0
  6 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33  4  1  0
 14  8  1  0
 25 17  1  0
 28 12  1  0
  3 35  1  0
  4 36  1  6
  6 37  1  6
  9 38  1  0
 11 39  1  0
 14 40  1  0
 16 41  1  1
 18 42  1  0
 20 43  1  0
 22 44  1  0
 24 45  1  0
 25 46  1  0
 26 47  1  1
 27 48  1  0
 28 49  1  0
 28 50  1  0
 29 51  1  6
 30 52  1  0
 31 53  1  6
 32 54  1  0
 33 55  1  1
 34 56  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(-)-Epigallocatechin 7-O-glucuronide	HMDB
(2S,3S,4S,5R,6S)-6-{[(2R,3R)-3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylate	HMDB

Chemical Formula

C₂₁H₂₂O₁₃

Average Molecular Weight

482.3916

Monoisotopic Molecular Weight

482.10604079

IUPAC Name

(2S,3S,4S,5R,6S)-6-{[(2R,3R)-3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

(2S,3S,4S,5R,6S)-6-{[(2R,3R)-3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

O[C@@H]1CC2=C(O[C@@H]1C1=CC(O)=C(O)C(O)=C1)C=C(O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)C=C2O

InChI Identifier

InChI=1S/C21H22O13/c22-9-3-7(32-21-17(29)15(27)16(28)19(34-21)20(30)31)4-13-8(9)5-12(25)18(33-13)6-1-10(23)14(26)11(24)2-6/h1-4,12,15-19,21-29H,5H2,(H,30,31)/t12-,15+,16+,17-,18-,19+,21-/m1/s1

InChI Key

DMDNCGKEYCRXOR-CVPXIJHMSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glucuronides

Alternative Parents

Substituents

Flavonoid-7-o-glucuronide
Epigallocatechin
Flavonoid-7-o-glycoside
Catechin
3'-hydroxyflavonoid
3-hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
Hydroxyflavonoid
Flavan-3-ol
Flavan
Phenolic glycoside
O-glucuronide
1-o-glucuronide
Glucuronic acid or derivatives
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Chromane
Benzopyran
1-benzopyran
Benzenetriol
Pyrogallol derivative
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Beta-hydroxy acid
Phenol
Monosaccharide
Hydroxy acid
Pyran
Oxane
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Monocarboxylic acid or derivatives
Acetal
Polyol
Ether
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organic oxide
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Blood (HMDB: HMDB0041640)
Urine (HMDB: HMDB0041640)

Organ

Liver (HMDB: HMDB0041640)
Kidney (HMDB: HMDB0041640)

Excreta

Biofluid or Excreta

Urine (PMID: 18433082)

Non-excretory biofluid

Biofluid or Excreta

Blood (HMDB: HMDB0041640)

Cellular substructure

Extracellular (HMDB: HMDB0041640)
Cytoplasm (HMDB: HMDB0041640)

Source

Endogenous

Endogenous (HMDB: HMDB0041640)

Plant

Plant (HMDB: HMDB0041640)

Exogenous

Food

Food (HMDB: HMDB0041640)

Not Available

Nutrient (HMDB: HMDB0041640)

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	3.07 g/L	ALOGPS
logP	0.37	ALOGPS
logP	-0.46	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	2.84	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	226.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	107.99 m³·mol⁻¹	ChemAxon
Polarizability	45.33 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	207.962	31661259
DarkChem	[M-H]-	203.493	31661259
DeepCCS	[M+H]+	197.987	30932474
DeepCCS	[M-H]-	196.145	30932474
DeepCCS	[M-2H]-	229.559	30932474
DeepCCS	[M+Na]+	203.593	30932474
AllCCS	[M+H]+	208.6	32859911
AllCCS	[M+H-H2O]+	206.5	32859911
AllCCS	[M+NH4]+	210.5	32859911
AllCCS	[M+Na]+	211.1	32859911
AllCCS	[M-H]-	204.2	32859911
AllCCS	[M+Na-2H]-	204.9	32859911
AllCCS	[M+HCOO]-	205.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(-)-Epigallocatechin 7-glucuronide	O[C@@H]1CC2=C(O[C@@H]1C1=CC(O)=C(O)C(O)=C1)C=C(O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)C=C2O	5825.7	Standard polar	33892256
(-)-Epigallocatechin 7-glucuronide	O[C@@H]1CC2=C(O[C@@H]1C1=CC(O)=C(O)C(O)=C1)C=C(O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)C=C2O	4185.2	Standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide	O[C@@H]1CC2=C(O[C@@H]1C1=CC(O)=C(O)C(O)=C1)C=C(O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)C=C2O	4526.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(-)-Epigallocatechin 7-glucuronide,1TMS,isomer #1	C[Si](C)(C)O[C@@H]1CC2=C(O)C=C(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O)C=C2O[C@@H]1C1=CC(O)=C(O)C(O)=C1	4420.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TMS,isomer #2	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4372.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TMS,isomer #3	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)C=C1O	4351.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O	4411.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@H]1O	4401.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TMS,isomer #6	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	4419.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TMS,isomer #7	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4370.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TMS,isomer #8	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4355.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #1	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4289.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #10	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4228.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #11	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4260.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #12	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4210.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #13	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4230.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #14	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C	4197.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #15	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4209.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #16	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)C=C1O	4198.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #17	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)C=C1O	4173.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #18	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)C=C1O	4199.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #19	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4188.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4310.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #20	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4310.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #21	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4277.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #22	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H]1O	4328.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #23	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O[Si](C)(C)C	4311.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #24	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@@H]1O[Si](C)(C)C	4309.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #25	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4253.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #26	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4297.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #27	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4279.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #28	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4316.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #29	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4248.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #3	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O	4335.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@H]1O	4317.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #5	C[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	4334.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #6	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4263.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #7	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	4198.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4235.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TMS,isomer #9	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4261.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4171.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4209.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4227.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #12	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4153.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #13	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	4072.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #14	C[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@H]1O	4248.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #15	C[Si](C)(C)O[C@@H]1CC2=C(O)C=C(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C=C2O[C@@H]1C1=CC(O)=C(O)C(O)=C1	4227.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #16	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@@H]1O[Si](C)(C)C	4219.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #17	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4123.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #18	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	4040.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #19	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4151.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #2	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4205.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #20	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	4064.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #21	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	4093.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #22	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	4072.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #23	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4081.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #24	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4095.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #25	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4067.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #26	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4141.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #27	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4107.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #28	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4143.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #29	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4133.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #3	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4184.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #30	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4157.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #31	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4108.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #32	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4106.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #33	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C	4078.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #34	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4127.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #35	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4079.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #36	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4073.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #37	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C	4045.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #38	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4110.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #39	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4103.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #4	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4200.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #40	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C	4074.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #41	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4097.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #42	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4073.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #43	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4093.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #44	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4097.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #45	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4094.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #46	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4067.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #47	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4104.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #48	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)C=C1O	4066.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #49	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)C=C1O	4093.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #5	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4100.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #50	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4081.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #51	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)C=C1O	4059.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #52	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4058.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #53	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4074.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #54	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4186.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #55	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4242.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #56	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4217.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #57	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4184.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #58	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4199.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #59	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C	4226.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #6	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4063.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #60	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4211.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #61	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4180.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #62	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4163.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #63	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4185.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #7	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4129.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4080.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TMS,isomer #9	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4227.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	3988.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #10	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4122.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #11	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	3994.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #12	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4010.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #13	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4022.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #14	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4007.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #15	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	4042.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #16	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4017.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #17	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	3995.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #18	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	3973.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #19	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4059.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4005.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #20	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4022.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #21	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4054.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #22	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4004.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #23	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3990.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #24	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4001.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #25	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4181.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #26	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4213.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #27	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4182.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #28	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4065.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #29	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4086.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #3	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4131.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #30	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	4024.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #31	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	3996.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #32	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3992.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #33	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	4015.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #34	C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C	4189.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #35	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4059.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #36	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3986.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #37	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	3999.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #38	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	3978.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #39	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	4022.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4097.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #40	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	3995.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #41	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4043.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #42	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4046.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #43	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4019.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #44	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4026.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #45	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3989.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #46	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4021.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #47	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4001.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #48	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4041.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #49	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4006.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4122.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #50	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4035.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #51	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4009.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #52	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3984.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #53	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4003.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #54	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4061.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #55	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4095.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #56	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4062.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #57	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4085.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #58	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4034.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #59	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4043.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #6	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4131.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #60	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C	4010.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #61	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4051.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #62	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4061.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #63	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C	4031.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #64	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4066.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #65	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4033.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #66	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4046.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #67	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4033.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #68	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4038.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #69	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C	4006.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #7	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4147.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #70	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4037.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #71	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4017.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #72	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4009.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #73	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4063.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #74	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4033.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #75	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4043.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #76	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4058.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #77	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4042.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #78	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4036.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #79	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4044.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #8	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4022.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #80	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4025.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #81	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4055.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #82	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4025.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #83	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)C=C1O	4030.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #84	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4029.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #85	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4044.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #86	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4024.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #87	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4155.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #88	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4120.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #89	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4209.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #9	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4013.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #90	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4143.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,4TMS,isomer #91	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4123.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #1	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	3993.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4103.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4060.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #12	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4102.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #13	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	3982.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #14	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	3998.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #15	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	3997.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #16	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4012.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #17	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	4017.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #18	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	3993.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #19	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	3975.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	3975.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #20	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	3991.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #21	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	3992.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #22	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	3977.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #23	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	4006.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #24	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	3986.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #25	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C)[C@@H](C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4013.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #26	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	3993.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #27	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4013.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #28	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3983.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #29	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4004.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #3	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3981.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #30	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3996.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #31	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3969.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #32	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3989.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #33	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4011.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #34	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4042.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #35	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4010.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #36	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4002.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #37	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4022.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #38	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3998.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #39	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4185.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #4	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3951.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #40	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O	4044.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #41	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	4005.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #42	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	3988.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #43	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	4017.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #44	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	4003.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #45	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4018.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #46	C[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)C=C1O	3996.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #47	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	3997.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #48	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	3980.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #49	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	3985.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	3979.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #50	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4015.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #51	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4014.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #52	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4029.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #53	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4001.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #54	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4023.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #55	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4010.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #56	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3990.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #57	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4005.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #58	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3996.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #59	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4022.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4004.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #60	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3989.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #61	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4013.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #62	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3980.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #63	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4005.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #64	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4024.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #65	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4043.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #66	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4016.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #67	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4005.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #68	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4026.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #69	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3996.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #7	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	3984.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #70	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4067.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #71	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4021.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #72	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4040.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #73	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C	4019.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #74	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4029.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #75	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4007.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #76	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4015.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #77	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4039.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #78	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4019.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #79	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4033.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4002.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #80	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4034.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #81	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O	4021.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #82	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	3999.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #83	C[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]4O[Si](C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	4010.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #84	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4003.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #85	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	4033.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #86	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4019.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #87	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4043.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #88	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4015.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #89	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4036.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #9	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4066.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #90	C[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	4030.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,5TMS,isomer #91	C[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C)=C2)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4117.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H]1CC2=C(O)C=C(O[C@@H]3O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]3O)C=C2O[C@@H]1C1=CC(O)=C(O)C(O)=C1	4648.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4621.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)C=C1O	4601.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O	4638.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@H]1O	4630.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	4646.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4670.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4611.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4690.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4656.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4677.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4649.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O	4678.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C(C)(C)C	4662.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4698.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)C=C1O	4678.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)C=C1O	4659.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O)C=C1O	4682.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O2	4680.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4752.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4762.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4694.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4746.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4730.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@@H]1O[Si](C)(C)C(C)(C)C	4733.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4677.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4739.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4699.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4767.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4708.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@H]1O	4730.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@H]1O	4717.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@@H](O)[C@@H]1O	4730.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O	4656.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4643.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4688.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4678.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4791.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4804.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4839.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O	4729.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4748.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4816.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1CC2=C(O)C=C(O[C@@H]3O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C=C2O[C@@H]1C1=CC(O)=C(O)C(O)=C1	4797.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](C(=O)O)O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@@H]1O[Si](C)(C)C(C)(C)C	4796.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O	4701.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4727.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O	4731.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4767.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)C=C1O	4746.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1O	4746.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O[Si](C)(C)C(C)(C)C	4735.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)O3)C(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4759.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4786.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4778.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4779.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4750.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4778.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4736.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4739.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4757.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4739.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O	4781.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C(C)(C)C	4768.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O	4738.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4719.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O	4761.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C(C)(C)C	4750.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC(O)=C1O	4741.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O	4780.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=CC2=C1C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4763.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O)=CC(O)=C1O[Si](C)(C)C(C)(C)C	4770.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O	4791.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)O2	4781.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O)=C3C[C@H]2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)C	4783.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)O3)C(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O	4830.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4818.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4797.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4818.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #48	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O)=CC(O)=C3C[C@H]2O)C=C1O	4777.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #49	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O)C=C1O	4797.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]4O)=CC(O[Si](C)(C)C(C)(C)C)=C3C[C@H]2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O	4721.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #50	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O2	4814.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #51	CC(C)(C)[Si](C)(C)OC1=C(O)C=C([C@H]2OC3=CC(O[C@@H]4O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]4O[Si](C)(C)C(C)(C)C)=CC(O)=C3C[C@H]2O)C=C1O	4775.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #52	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O2	4802.4	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #53	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O2	4813.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #54	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4798.9	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #55	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4876.3	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #56	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4831.8	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #57	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4762.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #58	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4778.6	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #59	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)O[C@H](C(=O)O)[C@H]1O[Si](C)(C)C(C)(C)C	4819.7	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]2O)=CC2=C1C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O2	4774.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #60	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4832.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #61	CC(C)(C)[Si](C)(C)OC1=CC(O[C@@H]2O[C@H](C(=O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)=CC2=C1C[C@@H](O)[C@@H](C1=CC(O)=C(O)C(O)=C1)O2	4762.5	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #62	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4770.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #63	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC3=C(C[C@@H](O)[C@@H](C4=CC(O)=C(O)C(O)=C4)O3)C(O[Si](C)(C)C(C)(C)C)=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4802.1	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4752.0	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)OC3=C2)[C@H](O)[C@@H](O)[C@@H]1O	4771.2	Semi standard non polar	33892256
(-)-Epigallocatechin 7-glucuronide,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@H]1O[C@@H](OC2=CC(O)=C3C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C4=CC(O)=C(O)C(O)=C4)OC3=C2)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4841.8	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 - (-)-Epigallocatechin 7-glucuronide GC-MS (Non-derivatized) - 70eV, Positive	splash10-06vi-9108500000-0e77a4f3d7dcdd3947f1	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epigallocatechin 7-glucuronide GC-MS (3 TMS) - 70eV, Positive	splash10-001i-5230219000-ee58c4e515c1785ba14e	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (-)-Epigallocatechin 7-glucuronide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - (-)-Epigallocatechin 7-glucuronide 10V, Positive-QTOF	splash10-067r-0356900000-0692fd45265dc5a33e17	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 20V, Positive-QTOF	splash10-052r-0954100000-b986ad26b5af040ddd05	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 40V, Positive-QTOF	splash10-00di-0900000000-44322324ef1afb047210	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 10V, Negative-QTOF	splash10-0540-1214900000-28a34c2f451cb0385fdd	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 20V, Negative-QTOF	splash10-0ap0-2927500000-b3e6a302d98d263c85ef	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 40V, Negative-QTOF	splash10-0a6r-3934000000-8156590f9184508b32ac	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 10V, Positive-QTOF	splash10-053r-0014900000-cae14d6ff28a9e052fd2	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 20V, Positive-QTOF	splash10-067r-0529500000-6ac4c8b62d2734ae8fe9	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 40V, Positive-QTOF	splash10-02ar-1915100000-b0b8c4a9d8b8c8ab8913	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 10V, Negative-QTOF	splash10-001i-0100900000-75048265edf98a19e923	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 20V, Negative-QTOF	splash10-0k9i-4957600000-f0f58ba98f2b062c8305	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (-)-Epigallocatechin 7-glucuronide 40V, Negative-QTOF	splash10-052r-7559400000-dd222156eaf5ce965156	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Blood
Urine

Tissue Locations

Kidney
Liver

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Available	Not Available	Normal	Not Available	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Consuming polyphenols described by Phenol-Explorer entry 787	18433082	details

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

FDB029795

KNApSAcK ID

Not Available

Chemspider ID

30777582

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

76959109

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Neveu V, Perez-Jimenez J, Vos F, Crespy V, du Chaffaut L, Mennen L, Knox C, Eisner R, Cruz J, Wishart D, Scalbert A: Phenol-Explorer: an online comprehensive database on polyphenol contents in foods. Database (Oxford). 2010;2010:bap024. doi: 10.1093/database/bap024. Epub 2010 Jan 8. [PubMed:20428313 ]

Showing metabocard for (-)-Epigallocatechin 7-glucuronide (HMDB0041640)

MOL for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

3D MOL for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

3D SDF for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

3D-SDF for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

PDB for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

3D PDB for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

SMILES for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

INCHI for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

Structure for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

3D Structure for HMDB0041640 ((-)-Epigallocatechin 7-glucuronide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra