NP-MRD: Showing NP-Card for (8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate (NP0315988)

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Record Information

Version

2.0

Created at

2022-09-11 14:53:31 UTC

Updated at

2022-09-11 14:53:31 UTC

NP-MRD ID

NP0315988

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate

Description

(8R,9R,10R,11S,13R)-11-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]Tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate 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. (8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate is found in Balanophora japonica. Based on a literature review very few articles have been published on (8R,9R,10R,11S,13R)-11-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]Tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112216532D          

 56 62  0  0  1  0            999 V2000
    7.7596   -2.1759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5905   -1.3684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.0361   -0.0108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6509    0.5394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4818    1.3469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0966    1.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8804    1.6398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4952    2.1900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0495    0.8323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8333    0.5750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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 54 80  1  0
M  END


  Mrv1652309112216532D          

 56 62  0  0  1  0            999 V2000
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    9.8804    1.6398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4952    2.1900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.8333    0.5750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5810   -3.8299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9287   -5.6029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3313   -5.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5323   -6.0585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9226   -4.6885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7647   -3.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9347   -3.6171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5467   -2.8471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6197   -3.7124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8148   -4.5140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4417   -3.4588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9623   -2.7617    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7462   -3.0190    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9153   -3.8265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6991   -4.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3139   -3.5336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8682   -4.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6521   -5.1485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8212   -5.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6050   -6.2133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2064   -6.5062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3755   -7.3137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4226   -6.2489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8078   -6.7991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2535   -5.4414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3610   -2.4688    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1448   -2.7261    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  5 12  1  0  0  0  0
  2 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 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
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 29 36  2  0  0  0  0
 36 37  1  0  0  0  0
 21 37  1  0  0  0  0
 27 37  2  0  0  0  0
 35 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 41 40  1  6  0  0  0
 16 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  1  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
 52 53  1  0  0  0  0
 52 54  2  0  0  0  0
 46 54  1  0  0  0  0
 42 55  1  0  0  0  0
 14 55  1  0  0  0  0
 55 56  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0315988

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@H]1[C@H](OC(=O)\C=C\C2=CC=C(O)C(O)=C2)O[C@@H]2COC(=O)C3=CC(O)=C(O)C4=C3C3=C(O4)C(O)=C(O)C=C3C(=O)O[C@H]2[C@@H]1OC(=O)C1=CC(O)=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C36H26O20/c37-15-3-1-11(5-16(15)38)2-4-22(43)53-36-28(47)32(56-33(48)12-6-17(39)25(44)18(40)7-12)29-21(52-36)10-51-34(49)13-8-19(41)26(45)30-23(13)24-14(35(50)55-29)9-20(42)27(46)31(24)54-30/h1-9,21,28-29,32,36-42,44-47H,10H2/b4-2+/t21-,28-,29-,32-,36+/m1/s1

> <INCHI_KEY>
WUIXNJUCTSTFHT-MZCZBUJSSA-N

> <FORMULA>
C36H26O20

> <MOLECULAR_WEIGHT>
778.584

> <EXACT_MASS>
778.101743237

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
72.10751855474994

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(8R,9R,10R,11S,13R)-11-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0^{5,23}.0^{8,13}.0^{17,22}]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate

> <JCHEM_LOGP>
3.659918616

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.501819203278205

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.73744201191125

> <JCHEM_PKA_STRONGEST_BASIC>
-5.548940930615118

> <JCHEM_POLAR_SURFACE_AREA>
329.87000000000006

> <JCHEM_REFRACTIVITY>
181.896

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(8R,9R,10R,11S,13R)-11-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0^{5,23}.0^{8,13}.0^{17,22}]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  O   UNK     0      14.485  -4.062   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      14.169  -2.554   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.316  -1.527   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.001  -0.020   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.148   1.007   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.833   2.514   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.980   3.541   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.443   3.061   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      19.591   4.088   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      18.759   1.554   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      20.222   1.073   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      17.612   0.527   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.706  -2.074   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.558  -3.101   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.095  -2.621   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.947  -3.648   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.780  -2.579   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.211  -2.332   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.743  -2.945   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.051  -1.569   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.355  -3.769   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.261  -2.627   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.763  -2.984   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.287  -1.858   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.298  -4.463   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.206  -4.795   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.345  -5.612   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.085  -7.149   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.475  -7.866   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.843  -9.391   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.734 -10.459   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.352  -9.816   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.727 -11.309   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.455  -8.752   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.161  -7.218   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.611  -6.752   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.887  -5.315   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.757  -6.930   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       7.121  -8.426   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       8.291  -6.456   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       9.263  -5.155   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.726  -5.635   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      11.042  -7.143   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      12.505  -7.623   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      13.653  -6.596   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      12.821  -9.130   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      14.284  -9.611   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      14.600 -11.118   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      16.063 -11.598   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      13.452 -12.145   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      13.768 -13.652   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      11.989 -11.665   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      10.841 -12.692   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      11.673 -10.157   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      11.874  -4.608   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      13.337  -5.089   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    5                                                       
CONECT   13    2   14                                                       
CONECT   14   13   15   55                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   41                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   37                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   37                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   36                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   38                                                  
CONECT   36   35   29   37                                                  
CONECT   37   36   21   27                                                  
CONECT   38   35   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   16   42                                                  
CONECT   42   41   43   55                                                  
CONECT   43   42   44                                                       
CONECT   44   43   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   14   56                                                  
CONECT   56   55                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  124    0
END

View in JSmol

Synonyms

Value	Source
(8R,9R,10R,11S,13R)-11-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0,.0,.0,]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoic acid	Generator

Chemical Formula

C₃₆H₂₆O₂₀

Average Mass

778.5840 Da

Monoisotopic Mass

778.10174 Da

IUPAC Name

(8R,9R,10R,11S,13R)-11-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0^{5,23}.0^{8,13}.0^{17,22}]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate

Traditional Name

CAS Registry Number

Not Available

SMILES

O[C@H]1[C@H](OC(=O)\C=C\C2=CC=C(O)C(O)=C2)O[C@@H]2COC(=O)C3=CC(O)=C(O)C4=C3C3=C(O4)C(O)=C(O)C=C3C(=O)O[C@H]2[C@@H]1OC(=O)C1=CC(O)=C(O)C(O)=C1

InChI Identifier

InChI=1S/C36H26O20/c37-15-3-1-11(5-16(15)38)2-4-22(43)53-36-28(47)32(56-33(48)12-6-17(39)25(44)18(40)7-12)29-21(52-36)10-51-34(49)13-8-19(41)26(45)30-23(13)24-14(35(50)55-29)9-20(42)27(46)31(24)54-30/h1-9,21,28-29,32,36-42,44-47H,10H2/b4-2+/t21-,28-,29-,32-,36+/m1/s1

InChI Key

WUIXNJUCTSTFHT-MZCZBUJSSA-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
Balanophora 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
Hydroxycinnamic acid glycoside
Tetracarboxylic acid or derivatives
Galloyl ester
Dibenzofuran
Hydroxycinnamic acid or derivatives
Gallic acid or derivatives
Cinnamic acid ester
Coumaric acid or derivatives
Cinnamic acid or derivatives
M-hydroxybenzoic acid ester
Dihydroxybenzoic acid
P-hydroxybenzoic acid ester
P-hydroxybenzoic acid alkyl ester
Benzoate ester
Pyrogallol derivative
Benzoic acid or derivatives
Benzofuran
Benzenetriol
Catechol
Styrene
Benzoyl
Phenol
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
1-hydroxy-4-unsubstituted benzenoid
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Oxane
Monosaccharide
Furan
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Heteroaromatic compound
Secondary alcohol
Lactone
Carboxylic acid ester
Acetal
Polyol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Carbonyl group
Organic oxygen compound
Alcohol
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
logP	3.66	ChemAxon
pKa (Strongest Acidic)	6.74	ChemAxon
pKa (Strongest Basic)	-5.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	329.87 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	181.9 m³·mol⁻¹	ChemAxon
Polarizability	72.11 Å³	ChemAxon
Number of Rings	7	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

9643233

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11468403

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate (NP0315988)

MOL for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)

3D MOL for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)

3D SDF for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)

3D-SDF for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)

PDB for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)

3D PDB for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)

SMILES for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)

INCHI for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)

Structure for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)

3D Structure for NP0315988 ((8r,9r,10r,11s,13r)-11-{[(2e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3,10,19,20-pentahydroxy-6,16-dioxo-7,12,15,24-tetraoxapentacyclo[19.2.1.0⁵,²³.0⁸,¹³.0¹⁷,²²]tetracosa-1(23),2,4,17,19,21-hexaen-9-yl 3,4,5-trihydroxybenzoate)