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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:54:04 UTC

Update Date

2022-03-07 02:55:26 UTC

HMDB ID

HMDB0037651

Secondary Accession Numbers

HMDB37651

Metabolite Identification

Common Name

Epigallocatechin-(4beta->8)-catechin

Description

Epigallocatechin-(4beta->8)-catechin belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''. Epigallocatechin-(4beta->8)-catechin has been detected, but not quantified in, several different foods, such as barleys (Hordeum vulgare), broad beans (Vicia faba), common hazelnuts (Corylus avellana), and pomegranates (Punica granatum). This could make epigallocatechin-(4beta->8)-catechin a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Epigallocatechin-(4beta->8)-catechin.

Structure

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


  Mrv0541 05061309552D          

 43 48  0  0  0  0            999 V2000
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 42 29  1  0  0  0  0
 43 28  1  0  0  0  0
 43 30  1  0  0  0  0
M  END

HMDB0037651
     RDKit          3D
Epigallocatechin-(4beta->8)-catechin
 69 74  0  0  0  0  0  0  0  0999 V2000
    3.7973   -5.0461   -2.2147 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv0541 05061309552D          

 43 48  0  0  0  0            999 V2000
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    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1060   -2.9737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
 10  1  1  0  0  0  0
 10  3  2  0  0  0  0
 11  4  2  0  0  0  0
 11  5  1  0  0  0  0
 12  6  2  0  0  0  0
 12  7  1  0  0  0  0
 13  8  1  0  0  0  0
 14  2  1  0  0  0  0
 15  9  2  0  0  0  0
 15 13  1  0  0  0  0
 16  3  1  0  0  0  0
 16 14  2  0  0  0  0
 17  6  1  0  0  0  0
 18  9  1  0  0  0  0
 19  4  1  0  0  0  0
 20  5  2  0  0  0  0
 21  8  1  0  0  0  0
 22  7  2  0  0  0  0
 23 17  2  0  0  0  0
 23 22  1  0  0  0  0
 24 18  2  0  0  0  0
 25 23  1  0  0  0  0
 25 24  1  0  0  0  0
 26 19  2  0  0  0  0
 26 20  1  0  0  0  0
 27 25  1  0  0  0  0
 28 10  1  0  0  0  0
 28 21  1  0  0  0  0
 29 11  1  0  0  0  0
 29 27  1  0  0  0  0
 30 13  2  0  0  0  0
 30 24  1  0  0  0  0
 31 12  1  0  0  0  0
 32 14  1  0  0  0  0
 33 15  1  0  0  0  0
 34 16  1  0  0  0  0
 35 17  1  0  0  0  0
 36 18  1  0  0  0  0
 37 19  1  0  0  0  0
 38 20  1  0  0  0  0
 39 21  1  0  0  0  0
 40 26  1  0  0  0  0
 41 27  1  0  0  0  0
 42 22  1  0  0  0  0
 42 29  1  0  0  0  0
 43 28  1  0  0  0  0
 43 30  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037651

> <DATABASE_NAME>
hmdb

> <SMILES>
OC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C(C1C(O)C(OC3=CC(O)=CC(O)=C13)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C30H26O13/c31-12-6-17(35)23-22(7-12)42-29(11-4-19(37)26(40)20(38)5-11)27(41)25(23)24-18(36)9-15(33)13-8-21(39)28(43-30(13)24)10-1-2-14(32)16(34)3-10/h1-7,9,21,25,27-29,31-41H,8H2

> <INCHI_KEY>
ZYDDITZPGFXQSD-UHFFFAOYSA-N

> <FORMULA>
C30H26O13

> <MOLECULAR_WEIGHT>
594.5196

> <EXACT_MASS>
594.137340918

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_AVERAGE_POLARIZABILITY>
58.176177198980874

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-8-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

> <ALOGPS_LOGP>
2.22

> <JCHEM_LOGP>
2.812179691999999

> <ALOGPS_LOGS>
-3.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.074305970542673

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.56418332061728

> <JCHEM_PKA_STRONGEST_BASIC>
-5.176560376570383

> <JCHEM_POLAR_SURFACE_AREA>
240.98999999999995

> <JCHEM_REFRACTIVITY>
148.48890000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.76e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dihydroxyphenyl)-8-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037651
     RDKit          3D
Epigallocatechin-(4beta->8)-catechin
 69 74  0  0  0  0  0  0  0  0999 V2000
    3.7973   -5.0461   -2.2147 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0660   -3.9534   -1.7938 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7076   -3.8580   -2.0936 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9604   -2.7753   -1.6823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3845   -2.7339   -2.0089 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5343   -1.7398   -0.9540 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8726   -1.8631   -0.6754 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6398   -2.9299   -1.0724 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4436   -0.8235    0.0535 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9453    0.4917   -0.1011 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6748    1.3421    0.8905 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0253    1.1791    1.1119 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7555    1.9490    2.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1107    1.6882    2.1519 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1180    2.9137    2.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8065    3.7145    3.6540 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7577    3.0993    2.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1315    4.0837    3.2580 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0556    2.3297    1.6267 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4553    0.5672    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9710    1.7488   -0.5262 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7004   -0.5793   -0.5151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3397   -0.2434   -1.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0134    0.2787   -2.7243 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3369    0.4747   -3.0019 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9148    0.6206   -3.7021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2631    0.4205   -3.4190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2107    0.7529   -4.3765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6495   -0.0999   -2.2062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7054   -0.4196   -1.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1071   -0.9395   -0.0714 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3908   -1.3595    0.2517 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8806   -0.5415    1.3938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5202   -1.0669    2.4824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9334   -0.2238    3.4841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7084    1.1570    3.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1400    1.9554    4.4286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0671    1.6742    2.3090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8290    3.0443    2.1998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6499    0.8378    1.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3668   -1.3265   -0.8828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5480   -2.5938   -1.4405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0650   -0.3028   -1.9260 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9116   -5.8946   -1.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2913   -4.6813   -2.6624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7983   -3.4779   -2.5326 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6907   -2.9965   -0.8365 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2620    0.8473   -1.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5403    0.4070    0.5445 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7363    2.1715    2.7674 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7888    3.5891    3.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5799    4.6760    3.9248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9921    2.4983    1.4814 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2642    0.6775    1.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1221    2.0456   -0.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1180   -1.0289    0.3562 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6486    0.8530   -3.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5958    1.0293   -4.6519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9343    1.1342   -5.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3216   -2.4133    0.6252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6919   -2.1255    2.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4390   -0.6606    4.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6098    1.6204    5.2412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3619    3.4567    1.4117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427    1.2574    0.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3683   -1.0493   -0.4384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7982   -2.8570   -2.0272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5411    0.6729   -1.7103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5487   -0.6549   -2.8830 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  2  0
 10 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  2  0
 32 41  1  0
 41 42  1  0
 41 43  1  0
  8  2  1  0
 19 11  1  0
 30 23  1  0
 40 33  1  0
 22  6  1  0
 43 29  1  0
  1 44  1  0
  3 45  1  0
  5 46  1  0
  8 47  1  0
 10 48  1  0
 12 49  1  0
 14 50  1  0
 16 51  1  0
 18 52  1  0
 19 53  1  0
 20 54  1  0
 21 55  1  0
 22 56  1  0
 25 57  1  0
 26 58  1  0
 28 59  1  0
 32 60  1  0
 34 61  1  0
 35 62  1  0
 37 63  1  0
 39 64  1  0
 40 65  1  0
 41 66  1  0
 42 67  1  0
 43 68  1  0
 43 69  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.003  -5.390   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       9.534   0.161   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -0.198  -5.551   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
CONECT    1    2   10                                                       
CONECT    2    1   14                                                       
CONECT    3   10   16                                                       
CONECT    4   11   19                                                       
CONECT    5   11   20                                                       
CONECT    6   12   17                                                       
CONECT    7   12   22                                                       
CONECT    8   13   21                                                       
CONECT    9   15   18                                                       
CONECT   10    1    3   28                                                  
CONECT   11    4    5   29                                                  
CONECT   12    6    7   31                                                  
CONECT   13    8   15   30                                                  
CONECT   14    2   16   32                                                  
CONECT   15    9   13   33                                                  
CONECT   16    3   14   34                                                  
CONECT   17    6   23   35                                                  
CONECT   18    9   24   36                                                  
CONECT   19    4   26   37                                                  
CONECT   20    5   26   38                                                  
CONECT   21    8   28   39                                                  
CONECT   22    7   23   42                                                  
CONECT   23   17   22   25                                                  
CONECT   24   18   25   30                                                  
CONECT   25   23   24   27                                                  
CONECT   26   19   20   40                                                  
CONECT   27   25   29   41                                                  
CONECT   28   10   21   43                                                  
CONECT   29   11   27   42                                                  
CONECT   30   13   24   43                                                  
CONECT   31   12                                                            
CONECT   32   14                                                            
CONECT   33   15                                                            
CONECT   34   16                                                            
CONECT   35   17                                                            
CONECT   36   18                                                            
CONECT   37   19                                                            
CONECT   38   20                                                            
CONECT   39   21                                                            
CONECT   40   26                                                            
CONECT   41   27                                                            
CONECT   42   22   29                                                       
CONECT   43   28   30                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   96    0
END

COMPND    HMDB0037651
HETATM    1  O1  UNL     1       3.797  -5.046  -2.215  1.00  0.00           O  
HETATM    2  C1  UNL     1       3.066  -3.953  -1.794  1.00  0.00           C  
HETATM    3  C2  UNL     1       1.708  -3.858  -2.094  1.00  0.00           C  
HETATM    4  C3  UNL     1       0.960  -2.775  -1.682  1.00  0.00           C  
HETATM    5  O2  UNL     1      -0.384  -2.734  -2.009  1.00  0.00           O  
HETATM    6  C4  UNL     1       1.534  -1.740  -0.954  1.00  0.00           C  
HETATM    7  C5  UNL     1       2.873  -1.863  -0.675  1.00  0.00           C  
HETATM    8  C6  UNL     1       3.640  -2.930  -1.072  1.00  0.00           C  
HETATM    9  O3  UNL     1       3.444  -0.824   0.054  1.00  0.00           O  
HETATM   10  C7  UNL     1       2.945   0.492  -0.101  1.00  0.00           C  
HETATM   11  C8  UNL     1       3.675   1.342   0.891  1.00  0.00           C  
HETATM   12  C9  UNL     1       5.025   1.179   1.112  1.00  0.00           C  
HETATM   13  C10 UNL     1       5.756   1.949   2.019  1.00  0.00           C  
HETATM   14  O4  UNL     1       7.111   1.688   2.152  1.00  0.00           O  
HETATM   15  C11 UNL     1       5.118   2.914   2.730  1.00  0.00           C  
HETATM   16  O5  UNL     1       5.807   3.714   3.654  1.00  0.00           O  
HETATM   17  C12 UNL     1       3.758   3.099   2.526  1.00  0.00           C  
HETATM   18  O6  UNL     1       3.132   4.084   3.258  1.00  0.00           O  
HETATM   19  C13 UNL     1       3.056   2.330   1.627  1.00  0.00           C  
HETATM   20  C14 UNL     1       1.455   0.567   0.034  1.00  0.00           C  
HETATM   21  O7  UNL     1       0.971   1.749  -0.526  1.00  0.00           O  
HETATM   22  C15 UNL     1       0.700  -0.579  -0.515  1.00  0.00           C  
HETATM   23  C16 UNL     1      -0.340  -0.243  -1.502  1.00  0.00           C  
HETATM   24  C17 UNL     1       0.013   0.279  -2.724  1.00  0.00           C  
HETATM   25  O8  UNL     1       1.337   0.475  -3.002  1.00  0.00           O  
HETATM   26  C18 UNL     1      -0.915   0.621  -3.702  1.00  0.00           C  
HETATM   27  C19 UNL     1      -2.263   0.420  -3.419  1.00  0.00           C  
HETATM   28  O9  UNL     1      -3.211   0.753  -4.376  1.00  0.00           O  
HETATM   29  C20 UNL     1      -2.650  -0.100  -2.206  1.00  0.00           C  
HETATM   30  C21 UNL     1      -1.705  -0.420  -1.280  1.00  0.00           C  
HETATM   31  O10 UNL     1      -2.107  -0.939  -0.071  1.00  0.00           O  
HETATM   32  C22 UNL     1      -3.391  -1.360   0.252  1.00  0.00           C  
HETATM   33  C23 UNL     1      -3.881  -0.542   1.394  1.00  0.00           C  
HETATM   34  C24 UNL     1      -4.520  -1.067   2.482  1.00  0.00           C  
HETATM   35  C25 UNL     1      -4.933  -0.224   3.484  1.00  0.00           C  
HETATM   36  C26 UNL     1      -4.708   1.157   3.403  1.00  0.00           C  
HETATM   37  O11 UNL     1      -5.140   1.955   4.429  1.00  0.00           O  
HETATM   38  C27 UNL     1      -4.067   1.674   2.309  1.00  0.00           C  
HETATM   39  O12 UNL     1      -3.829   3.044   2.200  1.00  0.00           O  
HETATM   40  C28 UNL     1      -3.650   0.838   1.301  1.00  0.00           C  
HETATM   41  C29 UNL     1      -4.367  -1.326  -0.883  1.00  0.00           C  
HETATM   42  O13 UNL     1      -4.548  -2.594  -1.440  1.00  0.00           O  
HETATM   43  C30 UNL     1      -4.065  -0.303  -1.926  1.00  0.00           C  
HETATM   44  H1  UNL     1       3.912  -5.895  -1.673  1.00  0.00           H  
HETATM   45  H2  UNL     1       1.291  -4.681  -2.662  1.00  0.00           H  
HETATM   46  H3  UNL     1      -0.798  -3.478  -2.533  1.00  0.00           H  
HETATM   47  H4  UNL     1       4.691  -2.997  -0.837  1.00  0.00           H  
HETATM   48  H5  UNL     1       3.262   0.847  -1.099  1.00  0.00           H  
HETATM   49  H6  UNL     1       5.540   0.407   0.545  1.00  0.00           H  
HETATM   50  H7  UNL     1       7.736   2.172   2.767  1.00  0.00           H  
HETATM   51  H8  UNL     1       6.789   3.589   3.809  1.00  0.00           H  
HETATM   52  H9  UNL     1       3.580   4.676   3.925  1.00  0.00           H  
HETATM   53  H10 UNL     1       1.992   2.498   1.481  1.00  0.00           H  
HETATM   54  H11 UNL     1       1.264   0.678   1.146  1.00  0.00           H  
HETATM   55  H12 UNL     1       0.122   2.046  -0.107  1.00  0.00           H  
HETATM   56  H13 UNL     1       0.118  -1.029   0.356  1.00  0.00           H  
HETATM   57  H14 UNL     1       1.649   0.853  -3.879  1.00  0.00           H  
HETATM   58  H15 UNL     1      -0.596   1.029  -4.652  1.00  0.00           H  
HETATM   59  H16 UNL     1      -2.934   1.134  -5.267  1.00  0.00           H  
HETATM   60  H17 UNL     1      -3.322  -2.413   0.625  1.00  0.00           H  
HETATM   61  H18 UNL     1      -4.692  -2.126   2.543  1.00  0.00           H  
HETATM   62  H19 UNL     1      -5.439  -0.661   4.340  1.00  0.00           H  
HETATM   63  H20 UNL     1      -5.610   1.620   5.241  1.00  0.00           H  
HETATM   64  H21 UNL     1      -3.362   3.457   1.412  1.00  0.00           H  
HETATM   65  H22 UNL     1      -3.143   1.257   0.439  1.00  0.00           H  
HETATM   66  H23 UNL     1      -5.368  -1.049  -0.438  1.00  0.00           H  
HETATM   67  H24 UNL     1      -3.798  -2.857  -2.027  1.00  0.00           H  
HETATM   68  H25 UNL     1      -4.541   0.673  -1.710  1.00  0.00           H  
HETATM   69  H26 UNL     1      -4.549  -0.655  -2.883  1.00  0.00           H  
CONECT    1    2   44
CONECT    2    3    3    8
CONECT    3    4   45
CONECT    4    5    6    6
CONECT    5   46
CONECT    6    7   22
CONECT    7    8    8    9
CONECT    8   47
CONECT    9   10
CONECT   10   11   20   48
CONECT   11   12   12   19
CONECT   12   13   49
CONECT   13   14   15   15
CONECT   14   50
CONECT   15   16   17
CONECT   16   51
CONECT   17   18   19   19
CONECT   18   52
CONECT   19   53
CONECT   20   21   22   54
CONECT   21   55
CONECT   22   23   56
CONECT   23   24   24   30
CONECT   24   25   26
CONECT   25   57
CONECT   26   27   27   58
CONECT   27   28   29
CONECT   28   59
CONECT   29   30   30   43
CONECT   30   31
CONECT   31   32
CONECT   32   33   41   60
CONECT   33   34   34   40
CONECT   34   35   61
CONECT   35   36   36   62
CONECT   36   37   38
CONECT   37   63
CONECT   38   39   40   40
CONECT   39   64
CONECT   40   65
CONECT   41   42   43   66
CONECT   42   67
CONECT   43   68   69
END

HMDB0037651
     RDKit          3D
Epigallocatechin-(4beta->8)-catechin
 69 74  0  0  0  0  0  0  0  0999 V2000
    3.7973   -5.0461   -2.2147 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0660   -3.9534   -1.7938 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7076   -3.8580   -2.0936 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9604   -2.7753   -1.6823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3845   -2.7339   -2.0089 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5343   -1.7398   -0.9540 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8726   -1.8631   -0.6754 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6398   -2.9299   -1.0724 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4436   -0.8235    0.0535 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9453    0.4917   -0.1011 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6748    1.3421    0.8905 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0253    1.1791    1.1119 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7555    1.9490    2.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1107    1.6882    2.1519 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1180    2.9137    2.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8065    3.7145    3.6540 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7577    3.0993    2.5263 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1315    4.0837    3.2580 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0556    2.3297    1.6267 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4553    0.5672    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9710    1.7488   -0.5262 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7004   -0.5793   -0.5151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3397   -0.2434   -1.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0134    0.2787   -2.7243 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3369    0.4747   -3.0019 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9148    0.6206   -3.7021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2631    0.4205   -3.4190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2107    0.7529   -4.3765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6495   -0.0999   -2.2062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7054   -0.4196   -1.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1071   -0.9395   -0.0714 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3908   -1.3595    0.2517 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8806   -0.5415    1.3938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5202   -1.0669    2.4824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9334   -0.2238    3.4841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7084    1.1570    3.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1400    1.9554    4.4286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0671    1.6742    2.3090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8290    3.0443    2.1998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6499    0.8378    1.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3668   -1.3265   -0.8828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5480   -2.5938   -1.4405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0650   -0.3028   -1.9260 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9116   -5.8946   -1.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2913   -4.6813   -2.6624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7983   -3.4779   -2.5326 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6907   -2.9965   -0.8365 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2620    0.8473   -1.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5403    0.4070    0.5445 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7363    2.1715    2.7674 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7888    3.5891    3.8088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5799    4.6760    3.9248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9921    2.4983    1.4814 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2642    0.6775    1.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1221    2.0456   -0.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1180   -1.0289    0.3562 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6486    0.8530   -3.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5958    1.0293   -4.6519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9343    1.1342   -5.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3216   -2.4133    0.6252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6919   -2.1255    2.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4390   -0.6606    4.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6098    1.6204    5.2412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3619    3.4567    1.4117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1427    1.2574    0.4387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3683   -1.0493   -0.4384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7982   -2.8570   -2.0272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5411    0.6729   -1.7103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5487   -0.6549   -2.8830 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  2  0
 10 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  2  0
 34 35  1  0
 35 36  2  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  2  0
 32 41  1  0
 41 42  1  0
 41 43  1  0
  8  2  1  0
 19 11  1  0
 30 23  1  0
 40 33  1  0
 22  6  1  0
 43 29  1  0
  1 44  1  0
  3 45  1  0
  5 46  1  0
  8 47  1  0
 10 48  1  0
 12 49  1  0
 14 50  1  0
 16 51  1  0
 18 52  1  0
 19 53  1  0
 20 54  1  0
 21 55  1  0
 22 56  1  0
 25 57  1  0
 26 58  1  0
 28 59  1  0
 32 60  1  0
 34 61  1  0
 35 62  1  0
 37 63  1  0
 39 64  1  0
 40 65  1  0
 41 66  1  0
 42 67  1  0
 43 68  1  0
 43 69  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Epigallocatechin-(4b->8)-catechin	Generator
Epigallocatechin-(4β->8)-catechin	Generator
Epigallocatechin(4b->8)catechin	HMDB

Chemical Formula

C₃₀H₂₆O₁₃

Average Molecular Weight

594.5196

Monoisotopic Molecular Weight

594.137340918

IUPAC Name

2-(3,4-dihydroxyphenyl)-8-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

Traditional Name

2-(3,4-dihydroxyphenyl)-8-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol

CAS Registry Number

77983-30-3

SMILES

OC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C(C1C(O)C(OC3=CC(O)=CC(O)=C13)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O

InChI Identifier

InChI=1S/C30H26O13/c31-12-6-17(35)23-22(7-12)42-29(11-4-19(37)26(40)20(38)5-11)27(41)25(23)24-18(36)9-15(33)13-8-21(39)28(43-30(13)24)10-1-2-14(32)16(34)3-10/h1-7,9,21,25,27-29,31-41H,8H2

InChI Key

ZYDDITZPGFXQSD-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Biflavonoids and polyflavonoids

Direct Parent

Biflavonoids and polyflavonoids

Alternative Parents

Substituents

B-type proanthocyanidin
Bi- and polyflavonoid skeleton
Proanthocyanidin
Epigallocatechin
Catechin
3'-hydroxyflavonoid
Flavan-3-ol
Hydroxyflavonoid
3-hydroxyflavonoid
7-hydroxyflavonoid
5-hydroxyflavonoid
4'-hydroxyflavonoid
Flavan
Chromane
1-benzopyran
Benzopyran
Benzenetriol
Pyrogallol derivative
Catechol
Phenol
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Polyol
Organoheterocyclic compound
Oxacycle
Ether
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0037651)
Cytoplasm (HMDB: HMDB0037651)

Cytoplasm (HMDB: HMDB0037651)
Extracellular (HMDB: HMDB0037651)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037651)

Source

Exogenous

Food

Food (HMDB: HMDB0037651)

Cereal and cereal product

Cereals and cereal products (FooDB: FOOD00858)

Cereal

Barley (FooDB: FOOD00088)

Cereal product

Breakfast cereal (FooDB: FOOD00270)

Endogenous

Plant

Plant (HMDB: HMDB0037651)
Poaceae (HMDB: HMDB0037651)

Not Available

Nutrient (HMDB: HMDB0037651)

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	0.18 g/L	ALOGPS
logP	2.22	ALOGPS
logP	2.81	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	8.56	ChemAxon
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	240.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	148.49 m³·mol⁻¹	ChemAxon
Polarizability	58.18 Å³	ChemAxon
Number of Rings	6	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]+	234.299	31661259
DarkChem	[M-H]-	226.521	31661259
DeepCCS	[M-2H]-	253.658	30932474
DeepCCS	[M+Na]+	227.879	30932474
AllCCS	[M+H]+	238.6	32859911
AllCCS	[M+H-H2O]+	237.1	32859911
AllCCS	[M+NH4]+	240.0	32859911
AllCCS	[M+Na]+	240.4	32859911
AllCCS	[M-H]-	234.2	32859911
AllCCS	[M+Na-2H]-	236.0	32859911
AllCCS	[M+HCOO]-	238.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Epigallocatechin-(4beta->8)-catechin	OC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C(C1C(O)C(OC3=CC(O)=CC(O)=C13)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O	7490.1	Standard polar	33892256
Epigallocatechin-(4beta->8)-catechin	OC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C(C1C(O)C(OC3=CC(O)=CC(O)=C13)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O	5177.6	Standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin	OC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C(C1C(O)C(OC3=CC(O)=CC(O)=C13)C1=CC(O)=C(O)C(O)=C1)=C(O)C=C2O	6281.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #1	C[Si](C)(C)OC1CC2=C(O)C=C(O)C(C3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)=C2OC1C1=CC=C(O)C(O)=C1	5932.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #10	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5976.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #2	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5983.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #3	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	6004.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #4	C[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5935.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #5	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5994.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #6	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5988.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #7	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	5981.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #8	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O	5985.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TMS,isomer #9	C[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O)C(O)=C2)C1O	5977.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #1	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5796.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #10	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5825.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #11	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5827.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #12	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5818.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #13	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5863.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #14	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5828.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #15	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5870.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #16	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5804.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #17	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5809.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #18	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5848.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #19	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5857.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #2	C[Si](C)(C)OC1=CC(O)=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O)C(O)=C2)C1O	5804.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #20	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5852.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #21	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5890.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #22	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5850.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #23	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5893.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #24	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5828.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #25	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5797.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #26	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O	5838.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #27	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5821.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #28	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5809.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #29	C[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O)C(O)=C2)C1O[Si](C)(C)C	5800.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #3	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5820.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #30	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5787.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #31	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5815.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #32	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5847.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #33	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5888.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #34	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5840.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #35	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5838.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #36	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5826.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #37	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5817.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #38	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	5816.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #39	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5854.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #4	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5831.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #40	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	5822.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #41	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	5820.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #42	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5814.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #43	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O[Si](C)(C)C	5817.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #44	C[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O[Si](C)(C)C)C(O)=C2)C1O	5860.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #45	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5860.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #46	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5800.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #5	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O	5808.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #6	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O	5857.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #7	C[Si](C)(C)OC1CC2=C(O)C=C(O)C(C3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C)=C2OC1C1=CC=C(O)C(O)=C1	5760.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #8	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5835.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TMS,isomer #9	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5823.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #1	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5680.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #10	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5715.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #100	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5689.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #101	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5697.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #102	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5665.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #103	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5658.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #104	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5656.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #105	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5696.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #106	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O[Si](C)(C)C)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5710.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #107	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5700.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #108	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5687.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #109	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5743.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #11	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O	5681.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #110	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5719.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #111	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5714.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #112	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5734.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #113	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5706.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #114	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5726.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #115	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5711.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #116	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5680.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #117	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	5682.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #118	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5682.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #119	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	5694.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #12	C[Si](C)(C)OC1=CC(O)=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O[Si](C)(C)C)C(O)=C2)C1O	5694.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #120	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5682.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #121	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5697.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #122	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O[Si](C)(C)C	5677.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #123	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	5700.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #124	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5714.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #125	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O[Si](C)(C)C	5690.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #126	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5731.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #127	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5696.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #128	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5715.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #129	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5686.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #13	C[Si](C)(C)OC1=CC(O)=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O)C(O)=C2)C1O[Si](C)(C)C	5652.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #14	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5718.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #15	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5704.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #16	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5697.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #17	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5698.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #18	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5684.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #19	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5662.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #2	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5677.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #20	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O	5666.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #21	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5689.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #22	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5718.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #23	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5738.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #24	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5689.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #25	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2	5756.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #26	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2	5741.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #27	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5727.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #28	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5709.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #29	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5660.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #3	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5726.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #30	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5699.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #31	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O[Si](C)(C)C	5704.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #32	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5759.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #33	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5737.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #34	C[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)C=C1O	5699.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #35	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5687.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #36	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5675.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #37	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5715.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #38	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5697.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #39	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5693.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #4	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O	5690.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #40	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5740.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #41	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5714.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #42	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5688.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #43	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5670.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #44	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5736.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #45	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5686.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #46	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5719.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #47	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5700.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #48	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5684.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #49	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5667.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #5	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5711.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #50	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5728.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #51	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5705.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #52	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5674.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #53	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5650.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #54	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5652.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #55	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5713.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #56	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5716.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #57	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5691.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #58	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5704.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #59	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2	5767.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #6	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5649.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #60	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5722.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #61	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5695.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #62	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O	5675.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #63	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O[Si](C)(C)C	5733.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #64	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5683.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #65	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5738.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #66	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5687.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #67	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5716.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #68	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5713.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #69	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5759.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #7	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5723.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #70	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5735.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #71	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5721.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #72	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5696.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #73	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5710.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #74	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5743.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #75	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5725.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #76	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5721.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #77	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5693.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #78	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5730.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #79	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5701.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #8	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5708.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #80	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5686.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #81	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5679.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #82	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5741.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #83	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5721.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #84	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5732.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #85	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5746.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #86	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5726.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #87	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O	5704.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #88	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5717.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #89	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5698.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #9	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5678.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #90	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5655.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #91	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5667.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #92	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5673.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #93	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5688.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #94	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5680.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #95	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5703.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #96	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5662.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #97	C[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O[Si](C)(C)C)C(O)=C2)C1O[Si](C)(C)C	5660.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #98	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5674.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,3TMS,isomer #99	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5678.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #1	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5553.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #10	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5539.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #100	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5488.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #101	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5451.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #102	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5529.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #103	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5604.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #104	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5531.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #105	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5495.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #106	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5570.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #107	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2	5649.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #108	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5533.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #109	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5520.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #11	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5541.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #110	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O	5520.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #111	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O[Si](C)(C)C	5594.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #112	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5481.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #113	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5562.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #114	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5602.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #115	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5534.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #116	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5476.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #117	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5434.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #118	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5522.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #119	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5600.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #12	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5579.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #120	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5512.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #121	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5465.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #122	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5557.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #123	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2	5635.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #124	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5525.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #125	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5514.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #126	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O	5513.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #127	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O[Si](C)(C)C	5590.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #128	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5475.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #129	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5566.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #13	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5565.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #130	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5599.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #131	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5630.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #132	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5546.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #133	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5492.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #134	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5454.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #135	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5502.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #136	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5498.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #137	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O	5494.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #138	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O[Si](C)(C)C	5578.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #139	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5457.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #14	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5601.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #140	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5548.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #141	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5596.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #142	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5547.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #143	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5532.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #144	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5536.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #145	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2	5620.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #146	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5493.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #147	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2	5581.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #148	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2	5640.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #149	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5599.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #15	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5594.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #150	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O	5549.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #151	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O[Si](C)(C)C	5618.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #152	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O	5538.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #153	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O[Si](C)(C)C	5612.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #154	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5592.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #155	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5584.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #156	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5544.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #157	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5574.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #158	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5520.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #159	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5474.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #16	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5591.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #160	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5554.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #161	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O[Si](C)(C)C)C3=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5570.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #162	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5516.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #163	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5473.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #164	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5554.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #165	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5552.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #166	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5515.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #167	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5595.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #168	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5560.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #169	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5547.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #17	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2	5630.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #170	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O	5546.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #171	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5507.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #172	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5560.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #173	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5508.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #174	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5458.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #175	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5553.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #176	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5535.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #177	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5483.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #178	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5585.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #179	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5558.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #18	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2	5617.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #180	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5545.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #181	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O	5544.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #182	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5510.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #183	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5576.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #184	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5517.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #185	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5471.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #186	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5535.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #187	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5527.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #188	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O	5526.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #189	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5487.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #19	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5583.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #190	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5573.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #191	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5562.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #192	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5566.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #193	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2	5523.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #194	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5631.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #195	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O	5580.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #196	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O	5570.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #197	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5544.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #198	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5591.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #199	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5575.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #2	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5602.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #20	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5566.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #200	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5554.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #201	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5568.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #202	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5531.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #203	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5538.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #204	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5558.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #205	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5545.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #206	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5539.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #207	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5569.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #208	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5555.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #209	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5583.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #21	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5562.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #210	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5553.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #211	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5607.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #212	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5522.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #213	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5538.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #214	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5543.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #215	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5516.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #216	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5506.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #217	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5514.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #218	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5560.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #219	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O[Si](C)(C)C)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5568.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #22	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5608.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #220	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5570.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #221	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5532.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #222	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5554.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #223	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5536.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #224	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5514.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #225	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O[Si](C)(C)C)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5554.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #226	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O[Si](C)(C)C)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5527.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #227	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)O2	5563.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #228	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)O2	5565.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #229	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5644.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #23	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5575.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #230	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5580.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #231	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5602.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #232	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5575.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #233	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5593.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #234	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5553.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #235	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	5524.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #236	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	5529.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #237	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5498.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #238	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5551.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #239	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O[Si](C)(C)C	5552.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #24	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5545.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #240	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5566.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #241	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5550.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #242	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5606.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #243	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5573.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #244	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5551.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #245	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5614.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #246	C[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	5614.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #25	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5558.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #26	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5539.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #27	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5581.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #28	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5569.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #29	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5645.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #3	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O	5569.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #30	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5588.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #31	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5577.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #32	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5562.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #33	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5553.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #34	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O	5559.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #35	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O[Si](C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5561.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #36	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5589.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #37	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5590.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #38	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5584.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #39	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2	5620.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #4	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5548.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #40	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2	5606.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #41	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5579.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #42	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5560.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #43	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5557.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #44	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5601.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #45	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O[Si](C)(C)C	5593.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #46	C[Si](C)(C)OC1=CC(O)=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O[Si](C)(C)C)C(O)=C2)C1O[Si](C)(C)C	5542.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #47	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5558.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #48	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5534.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #49	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5582.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #5	C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	5548.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #50	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5570.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #51	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5639.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #52	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5604.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #53	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5592.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #54	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	5566.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #55	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)O2	5574.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #56	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5570.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #57	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5556.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #58	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O	5528.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #59	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5565.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #6	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	5584.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #60	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5629.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #61	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5538.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #62	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5508.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #63	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5555.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #64	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)=CC(O)=C1O	5539.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #65	C[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O[Si](C)(C)C)C(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)O2	5541.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #66	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O[Si](C)(C)C)=C1O	5584.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #67	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O[Si](C)(C)C	5580.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #68	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5627.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #69	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5619.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #7	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5569.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #70	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5578.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #71	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2	5605.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #72	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2	5588.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #73	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2	5575.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #74	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2	5577.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #75	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2	5559.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #76	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2	5617.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #77	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2	5603.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #78	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2	5683.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #79	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5613.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #8	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O[Si](C)(C)C)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5594.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #80	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O	5609.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #81	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O	5580.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #82	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O[Si](C)(C)C	5630.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #83	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5593.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #84	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5589.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #85	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O	5562.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #86	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1O	5582.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #87	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)=CC(O)=C1O[Si](C)(C)C	5568.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #88	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C	5637.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #89	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O	5584.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #9	C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C)=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC(O)=C1O	5563.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #90	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5637.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #91	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5561.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #92	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C	5610.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #93	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O[Si](C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	5513.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #94	C[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2	5549.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #95	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O	5491.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #96	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)C2O)=CC=C1O	5450.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #97	C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O	5529.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #98	C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C	5604.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,4TMS,isomer #99	C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1)C(C1=C(O)C=C(O[Si](C)(C)C)C3=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	5547.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1CC2=C(O)C=C(O)C(C3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O)=C2OC1C1=CC=C(O)C(O)=C1	6166.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	6160.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	6195.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	6207.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(C2=CC(O)=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	6175.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	6181.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6176.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	6183.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O	6222.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O)C(O)=C2)C1O	6167.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O2	6340.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	6373.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	6381.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	6376.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C2	6394.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)C2O)=CC=C1O	6376.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)C2O)=CC=C1O	6403.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C(C)(C)C)=CC=C1O	6356.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C(C)(C)C	6361.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	6383.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	6391.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O)C(O)=C2)C1O	6343.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	6387.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(O)C2	6405.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)C2O)C=C1O	6386.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)C2O)C=C1O	6416.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C(C)(C)C)C=C1O	6365.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C(C)(C)C)=CC(O)=C1O	6343.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C(C)(C)C)C=C1O	6373.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O[Si](C)(C)C(C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	6346.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O[Si](C)(C)C(C)(C)C)C(C1=CC(O)=C(O)C(O)=C1)O2	6344.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O)C(O)=C2)C1O[Si](C)(C)C(C)(C)C	6331.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C(C)(C)C)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6356.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O[Si](C)(C)C(C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	6327.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1)C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6354.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	6369.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	6405.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	6363.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C2	6364.3	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O)C(O)=C1)O2	6368.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	6354.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	6359.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(C1=C(O)C=C(O)C3=C1OC(C1=CC=C(O)C(O)=C1)C(O)C3)C(O)C(C1=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)O2	6388.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=C1)OC(C1=CC(O)=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C(C)(C)C)C2	6359.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	6361.8	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O	6356.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #42	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O[Si](C)(C)C(C)(C)C)=C1O	6364.0	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC(O)=C1O[Si](C)(C)C(C)(C)C	6360.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=C(O)C=C(O)C=C2OC(C2=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C2)C1O	6389.4	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	6386.6	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #46	CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O2	6335.9	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C(C)(C)C)C4)C2O)=CC(O)=C1O	6353.7	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2OC3=CC(O)=CC(O)=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C(C)(C)C)C4)C2O)C=C1O	6389.2	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1CC2=C(O)C=C(O)C(C3C4=C(O)C=C(O)C=C4OC(C4=CC(O)=C(O)C(O)=C4)C3O[Si](C)(C)C(C)(C)C)=C2OC1C1=CC=C(O)C(O)=C1	6316.1	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C(C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)C=C1O	6375.5	Semi standard non polar	33892256
Epigallocatechin-(4beta->8)-catechin,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C(C)(C)C)C(O)=CC(O)=C3C2C3=C(O)C=C(O)C=C3OC(C3=CC(O)=C(O)C(O)=C3)C2O)=CC=C1O	6370.4	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-(4beta->8)-catechin GC-MS (Non-derivatized) - 70eV, Positive	splash10-004r-0901360000-0d270010a0a92554c87c	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (1 TMS) - 70eV, Positive	splash10-0ukj-2800229000-b57e242ceca6defa14a2	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS ("Epigallocatechin-(4beta->8)-catechin,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Epigallocatechin-(4beta->8)-catechin GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-15	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-(4beta->8)-catechin 10V, Positive-QTOF	splash10-004j-0210890000-d3f1b63ce0854cd6aa16	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 20V, Positive-QTOF	splash10-0a4i-0645920000-bcb19ecd65e148082a5e	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 40V, Positive-QTOF	splash10-002o-0691110000-a30f2dab85889787c220	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 10V, Negative-QTOF	splash10-0006-0100290000-1036a550862ef2fa89d1	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 20V, Negative-QTOF	splash10-0udr-0920220000-7ad54b3ad8b8f8d15bcb	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 40V, Negative-QTOF	splash10-004i-0901000000-69ac0334da67612b4b76	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 10V, Negative-QTOF	splash10-0006-0000090000-d0a28a905b0faeed4e65	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 20V, Negative-QTOF	splash10-00mo-0000390000-add39244d120b7c3f498	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 40V, Negative-QTOF	splash10-0adr-0330290000-e5196e15877872627ac1	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 10V, Positive-QTOF	splash10-0002-0000290000-569e5cd826aaf0d0ee0b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 20V, Positive-QTOF	splash10-006t-0110690000-c34199abe029a7049284	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Epigallocatechin-(4beta->8)-catechin 40V, Positive-QTOF	splash10-000i-0902670000-dd37c53e6a95204bfb8c	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB016775

KNApSAcK ID

C00009113

Chemspider ID

35014448

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13831061

PDB ID

Not Available

ChEBI ID

169487

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for Epigallocatechin-(4beta->8)-catechin (HMDB0037651)

MOL for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

3D MOL for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

3D SDF for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

3D-SDF for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

PDB for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

3D PDB for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

SMILES for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

INCHI for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

Structure for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

3D Structure for HMDB0037651 (Epigallocatechin-(4beta->8)-catechin)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra