NP-MRD: Showing NP-Card for (2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal (NP0209765)

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Record Information

Version

2.0

Created at

2022-09-05 07:18:36 UTC

Updated at

2022-09-05 07:18:36 UTC

NP-MRD ID

NP0209765

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal

Description

Hexagalloylglucose belongs to the class of organic compounds known as linear diarylheptanoids. These are diarylheptanoids with an open heptane chain. The two aromatic rings are linked only by the heptane chain. (2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal is found in Paeonia lactiflora, Rhus chinensis and Rhus typhina. Based on a literature review very few articles have been published on hexagalloylglucose.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052209182D          

 78 83  0  0  1  0            999 V2000
    2.9885   -1.5110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3884   -2.2900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6973   -3.1635    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6522   -3.9744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8756   -3.4145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3526   -2.5865    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8224   -4.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5369   -4.7014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5369   -5.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2513   -5.9389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8224   -5.9389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8224   -6.7639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1079   -5.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3935   -5.9389    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5203   -3.7870    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.4340   -3.0158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2685   -2.6649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9870   -1.8894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5178   -1.2578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3646   -0.3693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3302   -1.4018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8044   -0.6697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6117   -2.1772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3933   -1.8096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0492   -4.8076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2437   -5.3268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.1607   -1.9945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.8365   -3.0532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.7364   -6.7825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6299   -6.4612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4880   -7.5692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3097   -8.1052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8656   -8.0768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8980   -8.9011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0562   -9.7812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2003   -9.3414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9072  -10.1536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4702   -8.9572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8170   -9.5662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4378   -8.1329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7392   -6.5789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1753   -5.7909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5520   -7.1578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3575   -6.9796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9147   -7.5880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8389   -7.4671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6663   -8.3747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9961   -9.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8608   -8.5530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2358   -9.3921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3037   -7.9446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  7 15  1  0  0  0  0
  3 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  6  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 20 28  1  0  0  0  0
 16 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  6  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
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 33 41  1  0  0  0  0
 29 42  1  0  0  0  0
 42 43  1  6  0  0  0
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 48 50  2  0  0  0  0
 50 51  1  0  0  0  0
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 52 53  1  0  0  0  0
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 46 54  1  0  0  0  0
 42 55  1  0  0  0  0
 55 56  1  0  0  0  0
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 59 60  2  0  0  0  0
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 76 77  1  0  0  0  0
 76 78  2  0  0  0  0
 70 78  1  0  0  0  0
M  END

     RDKit          3D

114119  0  0  0  0  0  0  0  0999 V2000
   -3.0371   -2.1787    0.3867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6654   -2.8265   -0.5555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6692   -2.2795   -1.4945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4111   -3.2970   -2.5258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3261   -1.3123   -2.3967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2151   -0.5894   -1.8187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1469   -1.0370   -3.8004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8922   -0.0111   -4.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7903    0.3057   -5.7147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5728    1.3522   -6.2489 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9224   -0.4038   -6.5031 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3011   -2.1209   -6.7768 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2969   -1.7193   -4.6139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3089   -2.0154   -1.0006 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2334   -1.3510   -2.1658 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4740   -3.3169   -1.0573 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3194   -5.5380   -0.6422 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2303    1.6066   -1.1741 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4004    4.2966   -0.6237 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309052209182D          

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M  END
> <DATABASE_ID>
NP0209765

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC(=CC(O)=C1O)C(=O)[C@](O)(C=O)[C@](O)(C(=O)C1=CC(O)=C(O)C(O)=C1)[C@@](O)(C(=O)C1=CC(O)=C(O)C(O)=C1)[C@@](O)(C(=O)C1=CC(O)=C(O)C(O)=C1)C(O)(C(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)C1=CC(O)=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C48H36O30/c49-13-44(74,38(68)14-1-20(50)32(62)21(51)2-14)46(76,41(71)17-7-26(56)35(65)27(57)8-17)48(78,43(73)19-11-30(60)37(67)31(61)12-19)47(77,42(72)18-9-28(58)36(66)29(59)10-18)45(75,39(69)15-3-22(52)33(63)23(53)4-15)40(70)16-5-24(54)34(64)25(55)6-16/h1-13,50-67,74-78H/t44-,46-,47-,48+/m1/s1

> <INCHI_KEY>
AGXNCMSMGJUERA-LUAHJADVSA-N

> <FORMULA>
C48H36O30

> <MOLECULAR_WEIGHT>
1092.786

> <EXACT_MASS>
1092.129139759

> <JCHEM_ACCEPTOR_COUNT>
30

> <JCHEM_ATOM_COUNT>
114

> <JCHEM_AVERAGE_POLARIZABILITY>
96.20593151947276

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
23

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4S,5S)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal

> <JCHEM_LOGP>
0.017868258999999997

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.897587060340498

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.517329317510134

> <JCHEM_PKA_STRONGEST_BASIC>
-6.037481481207878

> <JCHEM_POLAR_SURFACE_AREA>
584.7800000000002

> <JCHEM_REFRACTIVITY>
252.50650000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4S,5S)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  O   UNK     0       5.579  -2.821   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.325  -4.275   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.902  -5.905   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.817  -7.419   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.368  -6.374   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.391  -4.828   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.268  -8.006   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.602  -8.776   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.602 -10.316   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.936 -11.086   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.268 -11.086   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.268 -12.626   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.935 -10.316   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.601 -11.086   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.935  -8.776   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.438  -7.069   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.579  -7.855   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.180  -5.480   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.410  -5.630   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.835  -4.974   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.309  -3.527   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.300  -2.348   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.014  -0.689   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      11.816  -2.617   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      12.702  -1.250   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      12.342  -4.064   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      13.801  -3.378   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      11.351  -5.243   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.425  -8.974   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.922  -9.943   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      11.219  -8.856   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      12.914  -9.022   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      12.855  -7.750   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.815  -6.614   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.279  -5.145   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      11.500  -3.723   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      13.782  -4.813   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      14.904  -3.313   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      14.822  -5.948   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      16.495  -5.699   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      14.359  -7.417   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.438 -10.508   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       9.037 -11.173   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      12.064 -11.030   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      12.619  -9.532   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      13.764 -11.858   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      15.268 -11.525   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      16.308 -12.661   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      17.976 -12.061   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      15.844 -14.129   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      17.378 -15.130   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      14.341 -14.462   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      13.729 -16.224   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      13.301 -13.326   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      10.765 -12.159   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      10.420 -13.715   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0       9.212 -12.805   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0       7.642 -13.420   0.000  0.00  0.00           O+0
HETATM   59  C   UNK     0       9.586 -14.360   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      10.949 -15.077   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0      11.010 -16.615   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      11.305 -18.258   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0       9.707 -17.437   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0       9.160 -18.953   0.000  0.00  0.00           O+0
HETATM   65  C   UNK     0       8.344 -16.720   0.000  0.00  0.00           C+0
HETATM   66  O   UNK     0       7.125 -17.857   0.000  0.00  0.00           O+0
HETATM   67  C   UNK     0       8.284 -15.181   0.000  0.00  0.00           C+0
HETATM   68  C   UNK     0      12.580 -12.281   0.000  0.00  0.00           C+0
HETATM   69  O   UNK     0      13.394 -10.810   0.000  0.00  0.00           O+0
HETATM   70  C   UNK     0      14.097 -13.361   0.000  0.00  0.00           C+0
HETATM   71  C   UNK     0      15.601 -13.029   0.000  0.00  0.00           C+0
HETATM   72  C   UNK     0      16.641 -14.164   0.000  0.00  0.00           C+0
HETATM   73  O   UNK     0      18.366 -13.939   0.000  0.00  0.00           O+0
HETATM   74  C   UNK     0      16.177 -15.633   0.000  0.00  0.00           C+0
HETATM   75  O   UNK     0      16.793 -17.155   0.000  0.00  0.00           O+0
HETATM   76  C   UNK     0      14.673 -15.966   0.000  0.00  0.00           C+0
HETATM   77  O   UNK     0      15.374 -17.532   0.000  0.00  0.00           O+0
HETATM   78  C   UNK     0      13.633 -14.830   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   16                                             
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   15                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    7                                                       
CONECT   16    3   17   18   29                                             
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   20                                                       
CONECT   29   16   30   31   42                                             
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   41                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   33                                                       
CONECT   42   29   43   44   55                                             
CONECT   43   42                                                            
CONECT   44   42   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   54                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50   53   54                                                  
CONECT   53   52                                                            
CONECT   54   52   46                                                       
CONECT   55   42   56   57   68                                             
CONECT   56   55                                                            
CONECT   57   55   58   59                                                  
CONECT   58   57                                                            
CONECT   59   57   60   67                                                  
CONECT   60   59   61                                                       
CONECT   61   60   62   63                                                  
CONECT   62   61                                                            
CONECT   63   61   64   65                                                  
CONECT   64   63                                                            
CONECT   65   63   66   67                                                  
CONECT   66   65                                                            
CONECT   67   65   59                                                       
CONECT   68   55   69   70                                                  
CONECT   69   68                                                            
CONECT   70   68   71   78                                                  
CONECT   71   70   72                                                       
CONECT   72   71   73   74                                                  
CONECT   73   72                                                            
CONECT   74   72   75   76                                                  
CONECT   75   74                                                            
CONECT   76   74   77   78                                                  
CONECT   77   76                                                            
CONECT   78   76   70                                                       
MASTER        0    0    0    0    0    0    0    0   78    0  166    0
END

View in JSmol

Synonyms

Value	Source
3-O-Digalloyl-1,2,4,6-tetra-O-galloylglucose	MeSH

Chemical Formula

C₄₈H₃₆O₃₀

Average Mass

1092.7860 Da

Monoisotopic Mass

1092.12914 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1=CC(=CC(O)=C1O)C(=O)[C@](O)(C=O)[C@](O)(C(=O)C1=CC(O)=C(O)C(O)=C1)[C@@](O)(C(=O)C1=CC(O)=C(O)C(O)=C1)[C@@](O)(C(=O)C1=CC(O)=C(O)C(O)=C1)C(O)(C(=O)C1=CC(O)=C(O)C(O)=C1)C(=O)C1=CC(O)=C(O)C(O)=C1

InChI Identifier

InChI=1S/C48H36O30/c49-13-44(74,38(68)14-1-20(50)32(62)21(51)2-14)46(76,41(71)17-7-26(56)35(65)27(57)8-17)48(78,43(73)19-11-30(60)37(67)31(61)12-19)47(77,42(72)18-9-28(58)36(66)29(59)10-18)45(75,39(69)15-3-22(52)33(63)23(53)4-15)40(70)16-5-24(54)34(64)25(55)6-16/h1-13,50-67,74-78H/t44-,46-,47-,48+/m1/s1

InChI Key

AGXNCMSMGJUERA-LUAHJADVSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Paeonia lactiflora	LOTUS Database	35616633
Rhus chinensis	LOTUS Database	35616633
Rhus typhina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as linear diarylheptanoids. These are diarylheptanoids with an open heptane chain. The two aromatic rings are linked only by the heptane chain.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Diarylheptanoids

Sub Class

Linear diarylheptanoids

Direct Parent

Linear diarylheptanoids

Alternative Parents

Substituents

Linear 1,7-diphenylheptane skeleton
Dibenzylbutane lignan skeleton
Retro-dihydrochalcone
Norlignan skeleton
Cinnamylphenol
Linear 1,3-diarylpropanoid
Heptose monosaccharide
Alkyl-phenylketone
Butyrophenone
Phenylketone
Pyrogallol derivative
Benzenetriol
Aryl alkyl ketone
Aryl ketone
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monosaccharide
Beta-hydroxy ketone
Beta-hydroxy aldehyde
Monocyclic benzene moiety
Acyloin
Alpha-hydroxyaldehyde
Tertiary alcohol
Alpha-hydroxy ketone
Ketone
Polyol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

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	0.018	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

65793407

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

129630523

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal (NP0209765)

MOL for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)

3D MOL for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)

3D SDF for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)

3D-SDF for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)

PDB for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)

3D PDB for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)

SMILES for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)

INCHI for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)

Structure for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)

3D Structure for NP0209765 ((2r,3s,4s,5s)-2,3,4,5,6-pentahydroxy-7-oxo-2,3,4,5,6-pentakis(3,4,5-trihydroxybenzoyl)-7-(3,4,5-trihydroxyphenyl)heptanal)