NP-MRD: Showing NP-Card for 11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde (NP0189400)

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Record Information

Version

2.0

Created at

2022-09-04 05:52:35 UTC

Updated at

2022-09-04 05:52:36 UTC

NP-MRD ID

NP0189400

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde

Description

11-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]Nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]Octadeca-1(18),2,4,6,14,16-hexaene-10-carbaldehyde 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. Based on a literature review very few articles have been published on 11-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]Nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.02,7]Octadeca-1(18),2,4,6,14,16-hexaene-10-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042207522D          

 56 61  0  0  0  0            999 V2000
    2.4321   -5.5476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1169   -5.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8578   -5.4505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9138   -6.2736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5073   -6.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4868   -6.4940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7107   -7.4597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0259   -7.9198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0820   -8.7429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3972   -9.2030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8228   -9.1059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8789   -9.9290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5076   -8.6458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2485   -9.0088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4516   -7.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1364   -7.3626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0803   -6.5395    0.0000 C   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
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M  END

     RDKit          3D

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 50 76  1  0
 48 75  1  0
 46 74  1  0
 44 73  1  0
 40 72  1  0
 38 71  1  0
 36 70  1  0
 34 69  1  0
 29 68  1  1
 28 67  1  6
 24 66  1  0
 22 65  1  0
 20 64  1  0
 18 63  1  0
 14 62  1  0
 12 61  1  0
 10 60  1  0
  8 59  1  0
  3 58  1  6
  2 57  1  0
M  END


  Mrv1652309042207522D          

 56 61  0  0  0  0            999 V2000
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    3.9874   -2.9035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8977   -1.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1813   -1.0957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9940   -0.9539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6522   -0.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9357    0.3120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8394   -0.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3103    0.0284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5559   -1.3793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7431   -1.5211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1102   -2.0502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3355   -1.7667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1937   -0.9539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4189   -0.6704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8266   -0.4248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6848    0.3879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6014   -0.7083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8024    0.0918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2839   -2.2613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3633   -3.2123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8924   -3.8453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7877   -3.7289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7065   -2.9079    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  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
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
  3 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
 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
 39 41  2  0  0  0  0
 33 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  2  0  0  0  0
 42 49  1  0  0  0  0
 49 50  1  0  0  0  0
 43 51  1  0  0  0  0
 51 52  2  0  0  0  0
 51 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 29 55  1  0  0  0  0
 55 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0189400

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1COC(=O)C2=C(C(O)=C(O)C(O)=C2)C2=C(O)C(O)=C(O)C=C2C(=O)OC1C1OC(=O)C2=C(C(O)=C(O)C(O)=C2)C2=C(O)C(O)=C(O)C=C2C(=O)OC1C=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H24O22/c35-5-16-30(56-34(52)10-4-14(39)24(44)28(48)20(10)18-8(32(50)54-16)2-12(37)22(42)26(18)46)29-15(40)6-53-31(49)7-1-11(36)21(41)25(45)17(7)19-9(33(51)55-29)3-13(38)23(43)27(19)47/h1-5,15-16,29-30,36-48H,6H2

> <INCHI_KEY>
KHMBJGKOFANMAO-UHFFFAOYSA-N

> <FORMULA>
C34H24O22

> <MOLECULAR_WEIGHT>
784.544

> <EXACT_MASS>
784.075922413

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
68.63075140577968

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0^{2,7}]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0^{2,7}]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde

> <JCHEM_LOGP>
1.3180140636666662

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.688720021980695

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.250299294069935

> <JCHEM_PKA_STRONGEST_BASIC>
-6.173381861338453

> <JCHEM_POLAR_SURFACE_AREA>
385.26000000000005

> <JCHEM_REFRACTIVITY>
178.5608

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0^{2,7}]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0^{2,7}]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  O   UNK     0       4.540 -10.356   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.818  -9.497   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.201 -10.174   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.306 -11.711   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.414 -11.796   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.242 -12.122   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.793 -13.925   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.515 -14.784   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.620 -16.320   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.341 -17.179   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.003 -16.998   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.107 -18.534   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.281 -16.139   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.664 -16.816   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.176 -14.602   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.455 -13.744   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.350 -12.207   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.628 -11.348   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.011 -12.026   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      15.289 -11.167   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      14.116 -13.562   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      15.499 -14.240   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.837 -14.421   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.942 -15.958   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.967 -11.530   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.689 -12.388   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       9.862  -9.993   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.479  -9.315   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.375  -7.779   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.556  -6.791   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.982  -5.362   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.443  -5.420   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       9.492  -3.756   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.009  -3.492   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.538  -2.045   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      13.056  -1.781   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      10.551  -0.864   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      11.080   0.582   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       9.034  -1.128   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       8.046   0.053   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       8.504  -2.575   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.987  -2.839   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.806  -3.827   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.360  -3.298   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.095  -1.781   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       2.649  -1.251   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       5.276  -0.793   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       5.012   0.724   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       6.723  -1.322   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       7.098   0.171   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       6.458  -4.286   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       7.997  -4.221   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0       4.411  -5.996   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0       5.399  -7.178   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       7.070  -6.961   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0       6.919  -5.428   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    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   16                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   16   24                                                  
CONECT   24   23                                                            
CONECT   25   17   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27    3   29                                                  
CONECT   29   28   30   55                                                  
CONECT   30   29   31                                                       
CONECT   31   30   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   42                                                  
CONECT   42   41   43   49                                                  
CONECT   43   42   44   51                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   42   50                                                  
CONECT   50   49                                                            
CONECT   51   43   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   29   56                                                  
CONECT   56   55                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  122    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₂₄O₂₂

Average Mass

784.5440 Da

Monoisotopic Mass

784.07592 Da

IUPAC Name

11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0^{2,7}]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0^{2,7}]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde

Traditional Name

CAS Registry Number

Not Available

SMILES

OC1COC(=O)C2=C(C(O)=C(O)C(O)=C2)C2=C(O)C(O)=C(O)C=C2C(=O)OC1C1OC(=O)C2=C(C(O)=C(O)C(O)=C2)C2=C(O)C(O)=C(O)C=C2C(=O)OC1C=O

InChI Identifier

InChI=1S/C34H24O22/c35-5-16-30(56-34(52)10-4-14(39)24(44)28(48)20(10)18-8(32(50)54-16)2-12(37)22(42)26(18)46)29-15(40)6-53-31(49)7-1-11(36)21(41)25(45)17(7)19-9(33(51)55-29)3-13(38)23(43)27(19)47/h1-5,15-16,29-30,36-48H,6H2

InChI Key

KHMBJGKOFANMAO-UHFFFAOYSA-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

Not Available

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
Benzenoid
Carboxylic acid ester
Lactone
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Polyol
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Aldehyde
Organooxygen compound
Carbonyl group
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	1.32	ChemAxon
pKa (Strongest Acidic)	7.25	ChemAxon
pKa (Strongest Basic)	-6.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	385.26 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	178.56 m³·mol⁻¹	ChemAxon
Polarizability	68.63 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

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

145100

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

165564

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde (NP0189400)

MOL for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)

3D MOL for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)

3D SDF for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)

3D-SDF for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)

PDB for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)

3D PDB for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)

SMILES for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)

INCHI for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)

Structure for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)

3D Structure for NP0189400 (11-{3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.0²,⁷]nonadeca-1(15),2,4,6,16,18-hexaen-10-yl}-3,4,5,16,17,18-hexahydroxy-8,13-dioxo-9,12-dioxatricyclo[12.4.0.0²,⁷]octadeca-1(14),2,4,6,15,17-hexaene-10-carbaldehyde)