NP-MRD: Showing NP-Card for Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate (NP0336352)

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Record Information

Version

2.0

Created at

2024-09-11 05:51:09 UTC

Updated at

2024-09-11 05:51:09 UTC

NP-MRD ID

NP0336352

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate

Description

Based on a literature review very few articles have been published on Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05262308232D          

 64 71  0  0  0  0            999 V2000
    4.6567   -3.8553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6671   -2.8449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2401   -4.4386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2504   -3.4282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8702   -3.0584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0369   -4.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.5737    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6203   -4.8085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -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
    2.0374    0.0862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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
    5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  2  0  0  0  0
 15  1  2  0  0  0  0
 15  2  1  0  0  0  0
 16  5  2  0  0  0  0
 16  6  1  0  0  0  0
 17  7  2  0  0  0  0
 17  8  1  0  0  0  0
 18  9  2  0  0  0  0
 18 10  1  0  0  0  0
 19  3  2  0  0  0  0
 19  4  1  0  0  0  0
 20 11  2  0  0  0  0
 20 12  1  0  0  0  0
 21 13  1  0  0  0  0
 22 11  1  0  0  0  0
 23 14  2  0  0  0  0
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 26  7  1  0  0  0  0
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 28  9  1  0  0  0  0
 29 10  2  0  0  0  0
 30 14  1  0  0  0  0
 30 21  2  0  0  0  0
 31 12  2  0  0  0  0
 32 13  1  0  0  0  0
 33 22  2  0  0  0  0
 33 31  1  0  0  0  0
 34 23  1  0  0  0  0
 35 33  1  0  0  0  0
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 36 21  1  0  0  0  0
 36 34  2  0  0  0  0
 37 24  2  0  0  0  0
 37 25  1  0  0  0  0
 38 26  2  0  0  0  0
 38 27  1  0  0  0  0
 39 28  2  0  0  0  0
 39 29  1  0  0  0  0
 40 16  1  0  0  0  0
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 46 20  1  0  0  0  0
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 63 32  1  0  0  0  0
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 64 42  1  0  0  0  0
 64 44  1  0  0  0  0
M  END


  Mrv2104 05262308232D          

 64 71  0  0  0  0            999 V2000
    4.6567   -3.8553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6671   -2.8449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2401   -4.4386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2504   -3.4282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 64 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0336352

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)C1OC2=CC(O)=CC(O)=C2C(C1OC(=O)C1=CC(O)=C(O)C(O)=C1)C1=C(O)C2=C(OC(C(C2)OC(=O)C2=CC(O)=C(O)C(O)=C2)C2=CC(O)=C(O)C(O)=C2)C=C1O

> <INCHI_IDENTIFIER>
InChI=1/C44H34O20/c45-19-3-1-15(2-4-19)41-42(64-44(60)18-9-28(53)39(58)29(54)10-18)35(33-22(47)11-20(46)12-31(33)62-41)34-23(48)14-30-21(36(34)55)13-32(40(61-30)16-5-24(49)37(56)25(50)6-16)63-43(59)17-7-26(51)38(57)27(52)8-17/h1-12,14,32,35,40-42,45-58H,13H2

> <INCHI_KEY>
BZQGRVQEWHQYDX-UHFFFAOYNA-N

> <FORMULA>
C44H34O20

> <MOLECULAR_WEIGHT>
882.736

> <EXACT_MASS>
882.164343495

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
84.64633806827072

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
14

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxybenzoyloxy)-3,4-dihydro-2H-1-benzopyran-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

> <JCHEM_LOGP>
6.284952780999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.320263827793818

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.771061159774384

> <JCHEM_PKA_STRONGEST_BASIC>
-5.548931352819228

> <JCHEM_POLAR_SURFACE_AREA>
354.28000000000003

> <JCHEM_REFRACTIVITY>
218.0374000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxybenzoyloxy)-3,4-dihydro-2H-1-benzopyran-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  C   UNK     0       8.693  -7.197   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.579  -5.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.782  -8.285   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.667  -6.399   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.337   6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.671   3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.091  -5.709   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.337   4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.269  -7.887   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.336   8.470   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.671   6.930   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      16.004   4.620   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.671  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      16.004   6.160   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      14.671  -0.770   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      12.003   3.850   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      12.358  -8.976   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0       3.803   0.161   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       5.335   9.240   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      10.669   9.240   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      14.671   8.470   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0      17.338   3.850   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0      13.337   1.540   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      16.004  -3.080   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   56  O   UNK     0       8.002  10.780   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      17.338   6.930   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0      16.004   0.000   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0      12.003   2.310   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      10.669  -4.620   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      10.669   4.620   0.000  0.00  0.00           O+0
HETATM   64  O   UNK     0       9.336  -2.310   0.000  0.00  0.00           O+0
CONECT    1    3   15                                                       
CONECT    2    4   15                                                       
CONECT    3    1   19                                                       
CONECT    4    2   19                                                       
CONECT    5   16   24                                                       
CONECT    6   16   25                                                       
CONECT    7   17   26                                                       
CONECT    8   17   27                                                       
CONECT    9   18   28                                                       
CONECT   10   18   29                                                       
CONECT   11   20   22                                                       
CONECT   12   20   31                                                       
CONECT   13   21   32                                                       
CONECT   14   23   30                                                       
CONECT   15    1    2   41                                                  
CONECT   16    5    6   40                                                  
CONECT   17    7    8   43                                                  
CONECT   18    9   10   44                                                  
CONECT   19    3    4   45                                                  
CONECT   20   11   12   46                                                  
CONECT   21   13   30   36                                                  
CONECT   22   11   33   47                                                  
CONECT   23   14   34   48                                                  
CONECT   24    5   37   49                                                  
CONECT   25    6   37   50                                                  
CONECT   26    7   38   51                                                  
CONECT   27    8   38   52                                                  
CONECT   28    9   39   53                                                  
CONECT   29   10   39   54                                                  
CONECT   30   14   21   61                                                  
CONECT   31   12   33   62                                                  
CONECT   32   13   40   63                                                  
CONECT   33   22   31   35                                                  
CONECT   34   23   35   36                                                  
CONECT   35   33   34   42                                                  
CONECT   36   21   34   55                                                  
CONECT   37   24   25   56                                                  
CONECT   38   26   27   57                                                  
CONECT   39   28   29   58                                                  
CONECT   40   16   32   61                                                  
CONECT   41   15   42   62                                                  
CONECT   42   35   41   64                                                  
CONECT   43   17   59   63                                                  
CONECT   44   18   60   64                                                  
CONECT   45   19                                                            
CONECT   46   20                                                            
CONECT   47   22                                                            
CONECT   48   23                                                            
CONECT   49   24                                                            
CONECT   50   25                                                            
CONECT   51   26                                                            
CONECT   52   27                                                            
CONECT   53   28                                                            
CONECT   54   29                                                            
CONECT   55   36                                                            
CONECT   56   37                                                            
CONECT   57   38                                                            
CONECT   58   39                                                            
CONECT   59   43                                                            
CONECT   60   44                                                            
CONECT   61   30   40                                                       
CONECT   62   31   41                                                       
CONECT   63   32   43                                                       
CONECT   64   42   44                                                       
MASTER        0    0    0    0    0    0    0    0   64    0  142    0
END

View in JSmol

Synonyms

Value	Source
Epiafzelechin-(4b->6)-epigallocatechin 3,3'-digallate	Generator
Epiafzelechin-(4b->6)-epigallocatechin 3,3'-digallic acid	Generator
Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallic acid	Generator
Epiafzelechin-(4β->6)-epigallocatechin 3,3'-digallate	Generator
Epiafzelechin-(4β->6)-epigallocatechin 3,3'-digallic acid	Generator

Chemical Formula

C₄₄H₃₄O₂₀

Average Mass

882.7360 Da

Monoisotopic Mass

882.16434 Da

IUPAC Name

6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxybenzoyloxy)-3,4-dihydro-2H-1-benzopyran-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate

Traditional Name

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)C1OC2=CC(O)=CC(O)=C2C(C1OC(=O)C1=CC(O)=C(O)C(O)=C1)C1=C(O)C2=C(OC(C(C2)OC(=O)C2=CC(O)=C(O)C(O)=C2)C2=CC(O)=C(O)C(O)=C2)C=C1O

InChI Identifier

InChI=1/C44H34O20/c45-19-3-1-15(2-4-19)41-42(64-44(60)18-9-28(53)39(58)29(54)10-18)35(33-22(47)11-20(46)12-31(33)62-41)34-23(48)14-30-21(36(34)55)13-32(40(61-30)16-5-24(49)37(56)25(50)6-16)63-43(59)17-7-26(51)38(57)27(52)8-17/h1-12,14,32,35,40-42,45-58H,13H2

InChI Key

BZQGRVQEWHQYDX-UHFFFAOYNA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	6.28	ChemAxon
pKa (Strongest Acidic)	7.77	ChemAxon
pKa (Strongest Basic)	-5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	14	ChemAxon
Polar Surface Area	354.28 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	218.04 m³·mol⁻¹	ChemAxon
Polarizability	84.65 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate (NP0336352)

MOL for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)

3D MOL for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)

3D SDF for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)

3D-SDF for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)

PDB for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)

3D PDB for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)

SMILES for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)

INCHI for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)

Structure for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)

3D Structure for NP0336352 (Epiafzelechin-(4beta->6)-epigallocatechin 3,3'-digallate)