NP-MRD: Showing NP-Card for (9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one (NP0330548)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 16:00:15 UTC

Updated at

2022-09-12 16:00:15 UTC

NP-MRD ID

NP0330548

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one

Description

(9S)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]Nonadeca-1(17),2,4,6(19),14(18),15-hexaen-7-one belongs to the class of organic compounds known as meta,meta-bridged biphenyls. These are cyclic diarylheptanoids where the two aryl groups are linked to each other by an ether group conjugated to their 3-position. (9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one is found in Rhoiptelea chiliantha. Based on a literature review very few articles have been published on (9S)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]Nonadeca-1(17),2,4,6(19),14(18),15-hexaen-7-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122218002D          

 26 28  0  0  1  0            999 V2000
    5.2813   -0.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2763    0.7027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5594    1.1109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5544    1.9359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9046    2.3833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1255    1.9272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8414    1.1526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8474    0.6941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8894   -0.1299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6240   -0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0170    1.1835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7915    1.9771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0487    2.4901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5034    1.8403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5973    1.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3541    0.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4481   -0.1274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0795    3.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3809    3.7534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8089    3.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8397    4.5245    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1411    4.9634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5691    4.9100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2677    4.4711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2368    3.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9354    3.2078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  5 26  1  0  0  0  0
M  END

     RDKit          2D

 50 52  0  0  0  0  0  0  0  0999 V2000
    3.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    2.5981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0000    2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7447    2.4218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1472    2.9537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6363    2.7729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1430    4.2240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7630    4.8120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5639    3.9109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1839    4.4988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8707    1.9208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9935    2.9155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5678    0.5926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5678   -0.9074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9704   -0.3755    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8707   -2.2356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6363   -3.0877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1472   -3.2685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7447   -2.7366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5000   -2.5981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0490   -0.5490    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4510   -2.0490    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000   -2.5981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0000    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5000    2.5981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0000    4.0981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0000    1.0981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7566    3.9751    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3422    5.1251    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5822    6.3010    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0031    5.9879    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5625    1.7154    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5451    0.4767    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4784   -1.7118    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1323   -1.3241    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0500   -2.5279    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3031   -3.3710    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5446   -3.8946    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4915   -4.2940    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5765   -4.4051    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4584   -4.2693    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5966   -3.9425    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3422   -3.2685    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  7 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 13 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
  8  3  1  0
 16 11  1  0
 26  5  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  6 31  1  0
 10 32  1  0
 10 33  1  0
 10 34  1  0
 12 35  1  0
 14 36  1  0
 15 37  1  0
 17 38  1  0
 20 39  1  0
 20 40  1  0
 21 41  1  1
 22 42  1  0
 23 43  1  0
 23 44  1  0
 24 45  1  0
 24 46  1  0
 25 47  1  0
 25 48  1  0
 26 49  1  0
 26 50  1  0
M  END


  Mrv1652309122218002D          

 26 28  0  0  1  0            999 V2000
    5.2813   -0.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2763    0.7027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5594    1.1109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5544    1.9359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9046    2.3833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1255    1.9272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8414    1.1526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8474    0.6941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8894   -0.1299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6240   -0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0170    1.1835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7915    1.9771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0487    2.4901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5034    1.8403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5973    1.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3541    0.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4481   -0.1274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0795    3.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3809    3.7534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8089    3.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8397    4.5245    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1411    4.9634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5691    4.9100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2677    4.4711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2368    3.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9354    3.2078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  5 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0330548

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=CC(=C1OC)C1=CC(=CC=C1O)C(=O)C[C@@H](O)CCCC2

> <INCHI_IDENTIFIER>
InChI=1S/C21H24O5/c1-25-20-10-13-5-3-4-6-15(22)12-19(24)14-7-8-18(23)16(11-14)17(9-13)21(20)26-2/h7-11,15,22-23H,3-6,12H2,1-2H3/t15-/m0/s1

> <INCHI_KEY>
HBPMCGRQMGSKIQ-HNNXBMFYSA-N

> <FORMULA>
C21H24O5

> <MOLECULAR_WEIGHT>
356.418

> <EXACT_MASS>
356.162373873

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
37.778889133796305

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9S)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1^{2,6}]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one

> <JCHEM_LOGP>
3.412337105333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.980765664188642

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.262714085558708

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7672535381156003

> <JCHEM_POLAR_SURFACE_AREA>
75.99

> <JCHEM_REFRACTIVITY>
99.6887

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(9S)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1^{2,6}]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       9.858  -0.228   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.849   1.312   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.511   2.074   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.502   3.614   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.289   4.449   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.834   3.597   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.304   2.152   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.182   1.296   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.260  -0.242   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.631  -0.943   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.765   2.209   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.344   3.691   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.958   4.648   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.940   3.435   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.115   1.905   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.528   1.292   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.703  -0.238   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.015   6.187   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.711   7.006   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.377   6.907   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.434   8.446   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.130   9.265   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.796   9.165   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.100   8.346   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.042   6.807   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.346   5.988   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   26                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    7   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16                                                            
CONECT   18   13   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    5                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₄O₅

Average Mass

356.4180 Da

Monoisotopic Mass

356.16237 Da

IUPAC Name

(9S)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1^{2,6}]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one

Traditional Name

(9S)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1^{2,6}]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one

CAS Registry Number

Not Available

SMILES

COC1=CC2=CC(=C1OC)C1=CC(=CC=C1O)C(=O)C[C@@H](O)CCCC2

InChI Identifier

InChI=1S/C21H24O5/c1-25-20-10-13-5-3-4-6-15(22)12-19(24)14-7-8-18(23)16(11-14)17(9-13)21(20)26-2/h7-11,15,22-23H,3-6,12H2,1-2H3/t15-/m0/s1

InChI Key

HBPMCGRQMGSKIQ-HNNXBMFYSA-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
Rhoiptelea chiliantha	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as meta,meta-bridged biphenyls. These are cyclic diarylheptanoids where the two aryl groups are linked to each other by an ether group conjugated to their 3-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Diarylheptanoids

Sub Class

Cyclic diarylheptanoids

Direct Parent

Meta,meta-bridged biphenyls

Alternative Parents

Substituents

Meta,meta-bridged biphenyl
Anisole
Aryl alkyl ketone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Ketone
Secondary alcohol
Ether
Hydrocarbon derivative
Alcohol
Organic oxide
Organic oxygen compound
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	3.41	ChemAxon
pKa (Strongest Acidic)	7.26	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	99.69 m³·mol⁻¹	ChemAxon
Polarizability	37.78 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

75554361

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

134835192

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one (NP0330548)

MOL for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)

3D MOL for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)

3D SDF for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)

3D-SDF for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)

PDB for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)

3D PDB for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)

SMILES for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)

INCHI for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)

Structure for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)

3D Structure for NP0330548 ((9s)-3,9-dihydroxy-16,17-dimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-7-one)