NP-MRD: Showing NP-Card for (8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one (NP0220362)

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Record Information

Version

2.0

Created at

2022-09-05 21:39:15 UTC

Updated at

2022-09-05 21:39:15 UTC

NP-MRD ID

NP0220362

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one

Description

(8S)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]Nonadeca-1(17),2,4,6(19),14(18),15-hexaen-9-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. (8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one is found in Morella nana. Based on a literature review very few articles have been published on (8S)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]Nonadeca-1(17),2,4,6(19),14(18),15-hexaen-9-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052223392D          

 29 31  0  0  1  0            999 V2000
    4.1582    0.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7656   -0.6381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1976   -1.3409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7928   -2.0181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2980   -2.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0892   -3.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4823   -1.9667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3018   -1.8718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3819   -0.5412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2048   -0.4833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1114   -3.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3339   -4.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8697   -4.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0450   -4.8972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6134   -4.1940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0065   -3.4687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7887   -4.2162    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3956   -4.9415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8271   -5.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3571   -3.5131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7503   -2.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3187   -2.0847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7118   -1.3594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2803   -0.6563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5365   -1.3372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9297   -0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -2.0403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5750   -2.7656    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
  7  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
  4 28  1  0  0  0  0
 28 29  2  0  0  0  0
 22 29  1  0  0  0  0
M  END

     RDKit          2D

 55 57  0  0  0  0  0  0  0  0999 V2000
   -5.6489    2.8970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4497    1.9959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6305    0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2423   -0.1427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4042   -1.0913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9921   -2.4713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1913   -1.5702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5713   -2.1581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0105   -0.0811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2096    0.8200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5896    0.2320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8714   -3.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0697   -5.2342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7707   -5.9842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2719   -6.0446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0833   -5.4016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0319   -6.5635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9844   -4.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4541   -3.9024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4488   -5.0251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2250   -2.7218    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
    1.5000    2.5981    0.0000 O   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
   -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
   -6.8480    3.7981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7478    4.0962    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5500    1.6978    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4113   -0.6655    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1454   -1.6051    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9696   -0.3559    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1776    1.6120    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1457   -0.5344    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9120   -5.0468    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3122   -3.5491    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4890   -6.6744    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4919   -5.7112    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4727   -7.4543    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8083   -7.0674    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1901   -7.0837    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6873   -7.4860    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6256   -5.5585    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4434   -6.1479    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5715   -4.0305    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4556   -6.1493    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3869   -1.7732    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6669   -3.1352    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
    0.7500    3.8971    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    3.8971    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
 20 19  1  0
 19 18  1  0
 18 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 24 26  2  0
 26 27  1  0
 26 28  1  0
 28 29  2  0
 28  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  1  0
  3  9  1  0
  9 10  1  0
 10 11  1  0
  9  7  2  0
  7  8  1  0
  7  6  1  0
  6 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
  6  5  2  0
 16 18  1  0
 29 22  1  0
  5  4  1  0
 20 47  1  0
 20 48  1  0
 20 49  1  0
 18 46  1  1
 21 50  1  0
 21 51  1  0
 23 52  1  0
 25 53  1  0
 27 54  1  0
 29 55  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
  8 34  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 15 45  1  0
  5 33  1  0
M  END


  Mrv1652309052223392D          

 29 31  0  0  1  0            999 V2000
    4.1582    0.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7656   -0.6381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1976   -1.3409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7928   -2.0181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2980   -2.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0892   -3.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4823   -1.9667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3018   -1.8718    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0206   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3819   -0.5412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2048   -0.4833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1114   -3.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3339   -4.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8697   -4.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0450   -4.8972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6134   -4.1940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0065   -3.4687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7887   -4.2162    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3956   -4.9415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8271   -5.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3571   -3.5131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7503   -2.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3187   -2.0847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7118   -1.3594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2803   -0.6563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5365   -1.3372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9297   -0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -2.0403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5750   -2.7656    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
  7  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
  4 28  1  0  0  0  0
 28 29  2  0  0  0  0
 22 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0220362

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1CC2=CC(O)=C(O)C(=C2)C2=C(OC)C(OC)=C(O)C(CCCCC1=O)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O7/c1-27-18-10-12-8-14(20(26)17(24)9-12)15-11-13(6-4-5-7-16(18)23)19(25)22(29-3)21(15)28-2/h8-9,11,18,24-26H,4-7,10H2,1-3H3/t18-/m0/s1

> <INCHI_KEY>
VSWSCBZOQFDYLA-SFHVURJKSA-N

> <FORMULA>
C22H26O7

> <MOLECULAR_WEIGHT>
402.443

> <EXACT_MASS>
402.167853177

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.755506580618174

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(8S)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1^{2,6}]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one

> <JCHEM_LOGP>
3.773235740333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.307701905206615

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.942348795796269

> <JCHEM_PKA_STRONGEST_BASIC>
-4.048505207287707

> <JCHEM_POLAR_SURFACE_AREA>
105.45

> <JCHEM_REFRACTIVITY>
108.23329999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(8S)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1^{2,6}]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       7.762   0.163   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.029  -1.191   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.836  -2.503   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.080  -3.767   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.023  -5.164   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.500  -5.600   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.234  -3.671   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.763  -3.494   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.372  -2.395   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.046  -1.010   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      11.582  -0.902   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.541  -7.140   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.090  -7.655   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.223  -9.100   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.684  -9.141   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.878  -7.829   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.612  -6.475   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.339  -7.870   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.605  -9.224   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.411 -10.537   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.533  -6.558   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.267  -5.204   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.462  -3.891   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.195  -2.538   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.390  -1.225   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.735  -2.496   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.469  -1.142   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.540  -3.809   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.807  -5.162   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   28                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    3   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    6   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26    4   29                                                  
CONECT   29   28   22                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₆O₇

Average Mass

402.4430 Da

Monoisotopic Mass

402.16785 Da

IUPAC Name

(8S)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1^{2,6}]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one

Traditional Name

(8S)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1^{2,6}]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one

CAS Registry Number

Not Available

SMILES

CO[C@H]1CC2=CC(O)=C(O)C(=C2)C2=C(OC)C(OC)=C(O)C(CCCCC1=O)=C2

InChI Identifier

InChI=1S/C22H26O7/c1-27-18-10-12-8-14(20(26)17(24)9-12)15-11-13(6-4-5-7-16(18)23)19(25)22(29-3)21(15)28-2/h8-9,11,18,24-26H,4-7,10H2,1-3H3/t18-/m0/s1

InChI Key

VSWSCBZOQFDYLA-SFHVURJKSA-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
Morella nana	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
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Ketone
Cyclic ketone
Dialkyl ether
Ether
Polyol
Organic oxide
Organic oxygen compound
Carbonyl group
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	3.77	ChemAxon
pKa (Strongest Acidic)	8.94	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.45 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	108.23 m³·mol⁻¹	ChemAxon
Polarizability	41.76 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

162917241

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one (NP0220362)

MOL for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)

3D MOL for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)

3D SDF for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)

3D-SDF for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)

PDB for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)

3D PDB for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)

SMILES for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)

INCHI for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)

Structure for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)

3D Structure for NP0220362 ((8s)-3,4,15-trihydroxy-8,16,17-trimethoxytricyclo[12.3.1.1²,⁶]nonadeca-1(17),2(19),3,5,14(18),15-hexaen-9-one)