NP-MRD: Showing NP-Card for (1r,3s,9r,10s,27r,28s,30r,35s,36s,37r,39s)-1,3,15,16,17,20,21,22,28,37,39-undecahydroxy-2,8,11,26,29,32,38-heptaoxanonacyclo[32.5.2.0³,³⁷.0⁶,³⁶.0⁹,³⁰.0¹⁰,²⁷.0¹³,¹⁸.0¹⁹,²⁴.0³⁵,³⁹]hentetraconta-5,13(18),14,16,19,21,23,34(41)-octaene-4,7,12,25,33,40-hexone (NP0232966)

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Record Information

Version

2.0

Created at

2022-09-06 14:23:07 UTC

Updated at

2022-09-06 14:23:07 UTC

NP-MRD ID

NP0232966

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,9r,10s,27r,28s,30r,35s,36s,37r,39s)-1,3,15,16,17,20,21,22,28,37,39-undecahydroxy-2,8,11,26,29,32,38-heptaoxanonacyclo[32.5.2.0³,³⁷.0⁶,³⁶.0⁹,³⁰.0¹⁰,²⁷.0¹³,¹⁸.0¹⁹,²⁴.0³⁵,³⁹]hentetraconta-5,13(18),14,16,19,21,23,34(41)-octaene-4,7,12,25,33,40-hexone

Description

(1R,3S,9R,10S,27R,28S,30R,35S,36S,37R,39S)-1,3,15,16,17,20,21,22,28,37,39-undecahydroxy-2,8,11,26,29,32,38-heptaoxanonacyclo[32.5.2.0³,³⁷.0⁶,³⁶.0⁹,³⁰.0¹⁰,²⁷.0¹³,¹⁸.0¹⁹,²⁴.0³⁵,³⁹]Hentetraconta-5,13,15,17,19,21,23,34(41)-octaene-4,7,12,25,33,40-hexone belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. (1r,3s,9r,10s,27r,28s,30r,35s,36s,37r,39s)-1,3,15,16,17,20,21,22,28,37,39-undecahydroxy-2,8,11,26,29,32,38-heptaoxanonacyclo[32.5.2.0³,³⁷.0⁶,³⁶.0⁹,³⁰.0¹⁰,²⁷.0¹³,¹⁸.0¹⁹,²⁴.0³⁵,³⁹]hentetraconta-5,13(18),14,16,19,21,23,34(41)-octaene-4,7,12,25,33,40-hexone is found in Carpinus japonica. Based on a literature review very few articles have been published on (1R,3S,9R,10S,27R,28S,30R,35S,36S,37R,39S)-1,3,15,16,17,20,21,22,28,37,39-undecahydroxy-2,8,11,26,29,32,38-heptaoxanonacyclo[32.5.2.0³,³⁷.0⁶,³⁶.0⁹,³⁰.0¹⁰,²⁷.0¹³,¹⁸.0¹⁹,²⁴.0³⁵,³⁹]Hentetraconta-5,13,15,17,19,21,23,34(41)-octaene-4,7,12,25,33,40-hexone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062216232D          

 58 66  0  0  1  0            999 V2000
    5.1515   -1.6683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.3192   -3.0214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.5749   -2.3395    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.3997   -2.3610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.4364   -1.2826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
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  9 34  1  0  0  0  0
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  5 35  1  0  0  0  0
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M  END

     RDKit          3D

 82 90  0  0  0  0  0  0  0  0999 V2000
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    5.1390   -0.2469   -1.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8951    3.1963   -1.4763 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7723    1.8686    2.3724 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 51  1  0
 51 50  2  0
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 48 46  1  0
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 46 45  1  0
 45 43  1  0
 43 44  1  6
 43 41  1  0
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 41 40  1  0
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 57 58  1  1
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  9  7  1  0
 35  5  1  0
  9 34  1  0
 52 51  1  0
 24 23  1  0
 13 21  1  0
 57 46  1  0
 54 43  1  0
 54 53  1  0
  8 63  1  0
  7 62  1  1
  5 61  1  6
  4 59  1  0
  4 60  1  0
 50 78  1  0
 47 77  1  0
 44 76  1  0
 40 75  1  0
 53 80  1  6
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 58 82  1  0
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 35 74  1  1
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 26 70  1  0
 24 69  1  0
 20 68  1  0
 18 67  1  0
 16 66  1  0
 14 65  1  0
  9 64  1  1
M  END


  Mrv1652309062216232D          

 58 66  0  0  1  0            999 V2000
    5.1515   -1.6683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3926   -2.9464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9255   -2.2964    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3192   -3.0214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1439   -3.0429    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5376   -3.7679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    9.3997   -2.3610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4807   -1.6570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4364   -1.2826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6554   -1.6791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0491   -2.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8738   -2.4256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2675   -3.1506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3048   -1.7222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1296   -1.7437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9111   -0.9972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3421   -0.2937    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0864   -0.9756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6927   -0.2506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8680   -0.2291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4743    0.4959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9053    1.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5116    1.9244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7300    1.1778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1610    1.8813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1237    0.4528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9484    0.4313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4370   -0.9325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8307   -1.6575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6123   -0.9110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1812   -1.6145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3565   -1.5929    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0969   -0.7722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3383   -0.3647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6657    0.3926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5012   -0.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2522    0.7490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4194    0.9448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2051    1.7415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7828    0.3439    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3280    1.0322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9596   -0.0151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7860   -0.9229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9778   -0.7572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5984   -1.7795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7965   -1.9734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1570   -2.4558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0051   -2.2982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3072   -1.5276    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8758   -0.7403    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2302   -0.2965    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8113    0.2891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9085   -1.0118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4440   -1.2197    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1356   -1.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
 23 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 34 33  1  6  0  0  0
  9 34  1  0  0  0  0
 34 35  1  0  0  0  0
  5 35  1  0  0  0  0
 35 36  1  1  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  6  0  0  0
 46 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 50 51  2  0  0  0  0
  2 51  1  0  0  0  0
 52 51  1  1  0  0  0
 52 53  1  0  0  0  0
 53 39  1  6  0  0  0
 53 54  1  0  0  0  0
 43 54  1  0  0  0  0
 54 55  1  6  0  0  0
 54 56  1  0  0  0  0
 56 57  1  0  0  0  0
 52 57  1  0  0  0  0
 46 57  1  0  0  0  0
 57 58  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0232966

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@H]1O[C@@H]2COC(=O)C3=CC(=O)[C@@]4(O)O[C@@]5(O)C(=O)C=C([C@@H]6[C@@H]3[C@]4(O)O[C@@]56O)C(=O)O[C@H]2[C@@H]2OC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(O)C(O)=C(O)C=C3C(=O)O[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C34H24O24/c35-10-1-6-15(21(41)19(10)39)16-7(2-11(36)20(40)22(16)42)28(45)56-25-24(55-27(6)44)23-12(53-30(25)47)5-52-26(43)8-3-13(37)31(48)33(50)17(8)18-9(29(46)54-23)4-14(38)32(49,57-31)34(18,51)58-33/h1-4,12,17-18,23-25,30,35-36,39-42,47-51H,5H2/t12-,17-,18-,23-,24+,25-,30+,31-,32+,33+,34-/m1/s1

> <INCHI_KEY>
BQJIXLFAHBDDSO-VVRHYXGBSA-N

> <FORMULA>
C34H24O24

> <MOLECULAR_WEIGHT>
816.542

> <EXACT_MASS>
816.065751653

> <ALOGPS_LOGP>
0.81

> <ALOGPS_LOGS>
-1.94

> <ALOGPS_SOLUBILITY>
9.38e+00 g/l

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  O   UNK     0       9.616  -3.114   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       9.064  -4.552   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.378  -5.394   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      11.933  -5.500   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.928  -4.287   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      13.663  -5.640   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      15.202  -5.680   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      15.937  -7.033   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      16.007  -4.367   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      17.546  -4.407   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      17.697  -3.093   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      17.615  -2.394   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      19.890  -3.134   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.625  -4.488   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      22.164  -4.528   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      22.899  -5.881   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      22.969  -3.215   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      24.509  -3.255   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      22.234  -1.861   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      23.039  -0.548   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      20.695  -1.821   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      19.960  -0.468   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      18.420  -0.428   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.685   0.926   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.490   2.239   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      17.755   3.592   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      20.029   2.199   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      20.834   3.512   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      20.764   0.845   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      22.304   0.805   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      17.616  -1.741   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      18.351  -3.094   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      16.076  -1.701   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      15.272  -3.014   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      13.732  -2.973   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      13.247  -1.442   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      11.832  -0.681   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      12.443   0.733   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      10.269  -0.158   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       9.804   1.398   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       8.250   1.764   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       7.850   3.251   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       7.061   0.642   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       6.212   1.927   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       5.525  -0.028   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       5.201  -1.723   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       3.692  -1.413   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       4.850  -3.322   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       3.354  -3.684   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       5.893  -4.584   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       7.476  -4.290   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       8.040  -2.852   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       9.102  -1.382   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       7.896  -0.553   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       8.981   0.540   0.000  0.00  0.00           O+0
HETATM   56  O   UNK     0       7.296  -1.889   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0       6.429  -2.277   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0       5.853  -3.705   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   51                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   35                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   34                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   13   22                                                  
CONECT   22   21   23   29                                                  
CONECT   23   22   24   31                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   22   30                                                  
CONECT   30   29                                                            
CONECT   31   23   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33    9   35                                                  
CONECT   35   34    5   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   53                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   45   54                                             
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45   47   48   57                                             
CONECT   47   46                                                            
CONECT   48   46   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   51                                                       
CONECT   51   50    2   52                                                  
CONECT   52   51   53   57                                                  
CONECT   53   52   39   54                                                  
CONECT   54   53   43   55   56                                             
CONECT   55   54                                                            
CONECT   56   54   57                                                       
CONECT   57   56   52   46   58                                             
CONECT   58   57                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  132    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₂₄O₂₄

Average Mass

816.5420 Da

Monoisotopic Mass

816.06575 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

O[C@H]1O[C@@H]2COC(=O)C3=CC(=O)[C@@]4(O)O[C@@]5(O)C(=O)C=C([C@@H]6[C@@H]3[C@]4(O)O[C@@]56O)C(=O)O[C@H]2[C@@H]2OC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(O)C(O)=C(O)C=C3C(=O)O[C@@H]12

InChI Identifier

InChI=1S/C34H24O24/c35-10-1-6-15(21(41)19(10)39)16-7(2-11(36)20(40)22(16)42)28(45)56-25-24(55-27(6)44)23-12(53-30(25)47)5-52-26(43)8-3-13(37)31(48)33(50)17(8)18-9(29(46)54-23)4-14(38)32(49,57-31)34(18,51)58-33/h1-4,12,17-18,23-25,30,35-36,39-42,47-51H,5H2/t12-,17-,18-,23-,24+,25-,30+,31-,32+,33+,34-/m1/s1

InChI Key

BQJIXLFAHBDDSO-VVRHYXGBSA-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
Carpinus japonica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Tetracarboxylic acid or derivatives
Gallic acid or derivatives
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Oxepane
Cyclohexenone
Monosaccharide
Oxane
Para-dioxane
Benzenoid
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Ketone
Lactone
Hemiacetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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

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

163194816

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]