NP-MRD: Showing NP-Card for (9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene (NP0309893)

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Record Information

Version

2.0

Created at

2022-09-11 04:47:46 UTC

Updated at

2022-09-11 04:47:46 UTC

NP-MRD ID

NP0309893

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene

Description

(9S,10R)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]Hexadeca-1(12),2,4,6,13,15-hexaene belongs to the class of organic compounds known as dibenzocyclooctadiene lignans. Dibenzocyclooctadiene lignans are compounds containing a dibenzocyclooctadiene moiety, which consists of two hydroxylated benzene connected by a cycloheptene ring. (9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene is found in Schisandra rubriflora. Based on a literature review very few articles have been published on (9S,10R)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]Hexadeca-1(12),2,4,6,13,15-hexaene.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112206472D          

 28 30  0  0  1  0            999 V2000
    4.6229    1.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8936    1.4086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0021    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7886    2.2053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    2.4188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084    1.8354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6219    1.0385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2912    0.0450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6743   -0.7273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4188    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0044    0.1145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602   -0.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834    1.8354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7969    2.2053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0104    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4271    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0103    0.1309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8149   -0.1649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3698    1.0385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8585    0.3705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7041   -0.5747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834    3.8271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2480    4.6186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084    3.8271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7377    4.6216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    3.2438    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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
  5 28  1  0  0  0  0
M  END

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
    5.2255   -0.2803   -1.4332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2965   -1.1410   -0.8325 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9711   -0.8152   -0.6296 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5421    0.4433   -1.0494 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2512    0.8323   -0.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3891   -0.0929   -0.2801 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7541   -1.3398    0.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2047   -2.1167    0.7610 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4681   -2.1450    2.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0712   -1.7000   -0.0262 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5536   -2.9229    0.3656 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1017   -3.2060    1.6293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0463   -0.0566   -0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8747    0.8909    0.5845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1719    0.5853    0.7442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6662   -0.6300    0.3154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8115   -1.5614   -0.2982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2728   -2.7949   -0.7434 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6455   -3.0833   -0.5557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4781   -1.2818   -0.4807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5428   -2.0958   -1.0885 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2827   -2.0959   -2.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5824    2.2742    1.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0656    3.0066   -0.1490 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6456    4.4207   -0.0326 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3600    3.0993   -0.3711 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0819    2.8958    0.9715 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0514    2.2146   -1.3549 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8763    0.0946   -2.4232 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2352   -0.7222   -1.4974 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3363    0.6352   -0.7906 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2207    1.1556   -1.5206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5483   -1.9470    2.2800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3426   -3.1911    2.5573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0842   -1.3951    2.7078 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9762   -2.3534    2.3331 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5533   -4.0668    2.0702 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1737   -3.5072    1.5770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8129    1.3396    1.2264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7160   -0.8788    0.4469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8977   -3.2537    0.5114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8964   -3.9959   -1.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2937   -2.2701   -0.9411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8396   -1.2636   -2.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8040   -1.9488   -2.6225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6017   -3.0908   -2.8849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5231    2.6879    1.4503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8115    2.1654    1.8607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5601    2.5936   -1.0789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2891    5.0634   -0.8506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7403    4.3861    0.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2409    4.8198    0.9363 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6273    4.1411   -0.6650 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6556    3.5771    1.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1194    3.2719    0.7895 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1125    1.8464    1.2631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0293    2.6311   -1.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4196    2.1720   -2.2652 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  1  0
  8  9  1  0
  7 10  2  0
 10 11  1  0
 11 12  1  0
  6 13  1  0
 13 14  2  0
 14 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  2  0
 20 21  1  0
 21 22  1  0
 10  3  1  0
 20 13  1  0
 28  5  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  4 32  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
 12 36  1  0
 12 37  1  0
 12 38  1  0
 23 47  1  0
 23 48  1  0
 24 49  1  6
 25 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  6
 27 54  1  0
 27 55  1  0
 27 56  1  0
 28 57  1  0
 28 58  1  0
 15 39  1  0
 16 40  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
 22 44  1  0
 22 45  1  0
 22 46  1  0
M  END


  Mrv1652309112206472D          

 28 30  0  0  1  0            999 V2000
    4.6229    1.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8936    1.4086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0021    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7886    2.2053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    2.4188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084    1.8354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6219    1.0385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2912    0.0450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6743   -0.7273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4188    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0044    0.1145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602   -0.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834    1.8354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7969    2.2053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0104    1.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4271    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0103    0.1309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8149   -0.1649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3698    1.0385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8585    0.3705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7041   -0.5747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834    3.8271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2480    4.6186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084    3.8271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7377    4.6216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    3.2438    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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
  5 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0309893

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C(OC)=C1OC)C1=C(C[C@@H](C)[C@@H](C)C2)C=CC(OC)=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O5/c1-13-10-15-8-9-17(24-3)21(26-5)19(15)20-16(11-14(13)2)12-18(25-4)22(27-6)23(20)28-7/h8-9,12-14H,10-11H2,1-7H3/t13-,14+/m1/s1

> <INCHI_KEY>
WMYDAFFJLZLKPE-KGLIPLIRSA-N

> <FORMULA>
C23H30O5

> <MOLECULAR_WEIGHT>
386.488

> <EXACT_MASS>
386.209324066

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
42.52761549413198

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9S,10R)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0^{2,7}]hexadeca-1(12),2(7),3,5,13,15-hexaene

> <JCHEM_LOGP>
4.858407248333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.219867140562473

> <JCHEM_POLAR_SURFACE_AREA>
46.150000000000006

> <JCHEM_REFRACTIVITY>
110.08959999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(9S,10R)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0^{2,7}]hexadeca-1(12),2(7),3,5,13,15-hexaene

> <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  C   UNK     0       8.630   3.484   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.268   2.629   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.604   2.629   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.205   4.116   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.718   4.515   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.629   3.426   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.028   1.939   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.410   0.084   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.125  -1.358   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.515   1.540   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.608   0.214   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.019  -0.563   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.089   3.426   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.000   4.515   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.488   4.116   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.886   2.629   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.797   1.540   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.886   0.244   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.388  -0.308   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.690   1.939   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.603   0.692   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.314  -1.073   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000   6.055   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.089   7.144   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.463   8.621   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.629   7.144   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.244   8.627   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.718   6.055   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7    3   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13    6   14   20                                                  
CONECT   14   13   15   23                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   13   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   14   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26    5                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₀O₅

Average Mass

386.4880 Da

Monoisotopic Mass

386.20932 Da

IUPAC Name

(9S,10R)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0^{2,7}]hexadeca-1(12),2(7),3,5,13,15-hexaene

Traditional Name

(9S,10R)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0^{2,7}]hexadeca-1(12),2(7),3,5,13,15-hexaene

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C(OC)=C1OC)C1=C(C[C@@H](C)[C@@H](C)C2)C=CC(OC)=C1OC

InChI Identifier

InChI=1S/C23H30O5/c1-13-10-15-8-9-17(24-3)21(26-5)19(15)20-16(11-14(13)2)12-18(25-4)22(27-6)23(20)28-7/h8-9,12-14H,10-11H2,1-7H3/t13-,14+/m1/s1

InChI Key

WMYDAFFJLZLKPE-KGLIPLIRSA-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
Schisandra rubriflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzocyclooctadiene lignans. Dibenzocyclooctadiene lignans are compounds containing a dibenzocyclooctadiene moiety, which consists of two hydroxylated benzene connected by a cycloheptene ring.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Dibenzocyclooctadiene lignans

Sub Class

Not Available

Direct Parent

Dibenzocyclooctadiene lignans

Alternative Parents

Substituents

Dibenzocyclooctane lignan
Anisole
Alkyl aryl ether
Benzenoid
Ether
Organic oxygen compound
Hydrocarbon derivative
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	4.86	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	46.15 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	110.09 m³·mol⁻¹	ChemAxon
Polarizability	42.53 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

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

162862758

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene (NP0309893)

MOL for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)

3D MOL for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)

3D SDF for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)

3D-SDF for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)

PDB for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)

3D PDB for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)

SMILES for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)

INCHI for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)

Structure for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)

3D Structure for NP0309893 ((9s,10r)-3,4,5,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaene)