NP-MRD: Showing NP-Card for 19,20-dihydroxyspongia-13(16),14-diene (NP0033783)

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Record Information

Version

2.0

Created at

2021-06-20 17:42:13 UTC

Updated at

2021-06-30 00:03:46 UTC

NP-MRD ID

NP0033783

Secondary Accession Numbers

None

Natural Product Identification

Common Name

19,20-dihydroxyspongia-13(16),14-diene

Provided By

JEOL Database JEOL Logo

Description

CHEMBL512451 belongs to the class of organic compounds known as isocopalane and spongiane diterpenoids. These are diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton. 19,20-dihydroxyspongia-13(16),14-diene is found in Spongia sp. 19,20-dihydroxyspongia-13(16),14-diene was first documented in 2008 (Carroll, A. R., et al.). Based on a literature review very few articles have been published on CHEMBL512451.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202119423D          

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     RDKit          3D

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  Mrv1652306202119423D          

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   -0.5124    0.1050   -1.8810 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8721   -0.9311   -2.1561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7785   -0.4762   -0.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4416    1.1207   -0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1983   -0.0605   -1.6869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6037    0.7333   -4.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7557    4.7980   -3.7117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4455    4.5045   -0.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1932    4.7415   -0.6492 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5395    2.7904    0.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1052    3.5339    1.3273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2725    2.0615   -0.2224 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 16  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 16  1  0  0  0  0
  6  5  1  0  0  0  0
  6  7  1  0  0  0  0
  5  2  1  0  0  0  0
  8 23  1  0  0  0  0
 11 12  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 12 13  1  0  0  0  0
 14 15  1  1  0  0  0
 13 14  1  0  0  0  0
  8  9  1  1  0  0  0
 23 14  1  0  0  0  0
  2  3  1  1  0  0  0
  2 11  1  0  0  0  0
  2  1  1  0  0  0  0
  8  7  1  0  0  0  0
 11 39  1  6  0  0  0
  8 11  1  0  0  0  0
 23 53  1  6  0  0  0
  9 10  1  0  0  0  0
 23 22  1  0  0  0  0
  3  4  1  0  0  0  0
  6 32  1  0  0  0  0
  6 33  1  0  0  0  0
  5 30  1  0  0  0  0
  5 31  1  0  0  0  0
  7 34  1  0  0  0  0
  7 35  1  0  0  0  0
 12 40  1  0  0  0  0
 12 41  1  0  0  0  0
 13 42  1  0  0  0  0
 13 43  1  0  0  0  0
 21 49  1  0  0  0  0
 21 50  1  0  0  0  0
 22 51  1  0  0  0  0
 22 52  1  0  0  0  0
 17 47  1  0  0  0  0
 19 48  1  0  0  0  0
 15 44  1  0  0  0  0
 15 45  1  0  0  0  0
 15 46  1  0  0  0  0
  9 36  1  0  0  0  0
  9 37  1  0  0  0  0
  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
 10 38  1  0  0  0  0
  4 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0033783

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])[C@@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]2(C([H])([H])O[H])[C@@]3([H])C([H])([H])C([H])([H])C4=C([H])OC([H])=C4[C@]3(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]12[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O3/c1-18(12-21)7-3-8-20(13-22)16(18)6-9-19(2)15-11-23-10-14(15)4-5-17(19)20/h10-11,16-17,21-22H,3-9,12-13H2,1-2H3/t16-,17-,18+,19-,20+/m0/s1

> <INCHI_KEY>
HJTMHDSGDBNZJV-UHZRXMQZSA-N

> <FORMULA>
C20H30O3

> <MOLECULAR_WEIGHT>
318.457

> <EXACT_MASS>
318.219494826

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
36.3860373672799

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1S,2S,6S,7S,10R)-6-(hydroxymethyl)-6,10-dimethyl-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-11,14-dien-2-yl]methanol

> <ALOGPS_LOGP>
3.42

> <JCHEM_LOGP>
3.190262925333333

> <ALOGPS_LOGS>
-4.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.592292739275248

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.090630393230132

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2136700385561943

> <JCHEM_POLAR_SURFACE_AREA>
53.6

> <JCHEM_REFRACTIVITY>
90.57089999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.62e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,2S,6S,7S,10R)-6-(hydroxymethyl)-6,10-dimethyl-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-11,14-dien-2-yl]methanol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 53 56  0  0  0  0  0  0  0  0999 V2000
   -2.6409   -1.9286    1.2467 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5324   -1.1052    1.9616 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7457   -2.0945    2.8577 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1252   -2.9420    2.1285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2707   -0.0829    2.8682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3626    0.9860    3.4632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5743    1.7383    2.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2583    0.8261    1.4335 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4548    0.2551    2.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4485    1.2383    2.4928 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7058   -0.3007    0.8864 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0200   -1.1453   -0.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3986   -0.2849   -1.4051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3348    0.8897   -1.0372 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7573    0.3429   -0.7657 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4611    1.8597   -2.2053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816    1.6264   -3.5587 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7059    2.7973   -4.2361 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6712    3.7957   -3.3159 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5252    3.2769   -2.0501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4096    3.9815   -0.7461 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4859    3.0077    0.4474 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6927    1.6949    0.1717 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3406   -2.3576    1.9740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2262   -1.3012    0.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2347   -2.7622    0.6670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1474   -1.5872    3.6135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4353   -2.7343    3.4228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4222   -3.5630    1.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7917   -0.6033    3.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0520    0.4240    2.2851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6877    0.5466    4.2039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9794    1.7056    4.0157 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0753    2.4605    2.8993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2897    2.3288    1.8035 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9274   -0.5955    1.7532 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1457   -0.0958    3.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1707    0.7953    2.9713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4897    0.2527    0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021   -1.9112   -0.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8510   -1.6784    0.1788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5124    0.1050   -1.8810 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8721   -0.9311   -2.1561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7785   -0.4762   -0.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4416    1.1207   -0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1983   -0.0605   -1.6869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6037    0.7333   -4.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7557    4.7980   -3.7117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4455    4.5045   -0.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1932    4.7415   -0.6492 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5395    2.7904    0.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1052    3.5339    1.3273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2725    2.0615   -0.2224 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 16  1  0
 20 21  1  0
 21 22  1  0
 20 16  1  0
  6  5  1  0
  6  7  1  0
  5  2  1  0
  8 23  1  0
 11 12  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 12 13  1  0
 14 15  1  1
 13 14  1  0
  8  9  1  1
 23 14  1  0
  2  3  1  1
  2 11  1  0
  2  1  1  0
  8  7  1  0
 11 39  1  6
  8 11  1  0
 23 53  1  6
  9 10  1  0
 23 22  1  0
  3  4  1  0
  6 32  1  0
  6 33  1  0
  5 30  1  0
  5 31  1  0
  7 34  1  0
  7 35  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 21 49  1  0
 21 50  1  0
 22 51  1  0
 22 52  1  0
 17 47  1  0
 19 48  1  0
 15 44  1  0
 15 45  1  0
 15 46  1  0
  9 36  1  0
  9 37  1  0
  3 27  1  0
  3 28  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 10 38  1  0
  4 29  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.641  -1.929   1.247  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.532  -1.105   1.962  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.746  -2.095   2.858  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.125  -2.942   2.128  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.271  -0.083   2.868  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.363   0.986   3.463  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.574   1.738   2.392  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.258   0.826   1.434  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.455   0.255   2.241  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.449   1.238   2.493  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.706  -0.301   0.886  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.020  -1.145  -0.208  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.399  -0.285  -1.405  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.335   0.890  -1.037  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.757   0.343  -0.766  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.461   1.860  -2.205  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.582   1.626  -3.559  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.706   2.797  -4.236  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.671   3.796  -3.316  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.525   3.277  -2.050  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.410   3.982  -0.746  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.486   3.008   0.447  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.693   1.695   0.172  0.00  0.00           C+0
HETATM   24  H   UNK     0      -3.341  -2.358   1.974  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.226  -1.301   0.565  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.235  -2.762   0.667  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.147  -1.587   3.614  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.435  -2.734   3.423  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.422  -3.563   1.618  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.792  -0.603   3.682  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.052   0.424   2.285  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.688   0.547   4.204  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.979   1.706   4.016  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.075   2.461   2.899  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.290   2.329   1.804  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.927  -0.596   1.753  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.146  -0.096   3.224  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.171   0.795   2.971  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.490   0.253   0.340  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.702  -1.911  -0.590  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.851  -1.678   0.179  0.00  0.00           H+0
HETATM   42  H   UNK     0      -0.512   0.105  -1.881  0.00  0.00           H+0
HETATM   43  H   UNK     0       0.872  -0.931  -2.156  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.779  -0.476  -0.050  0.00  0.00           H+0
HETATM   45  H   UNK     0       3.442   1.121  -0.414  0.00  0.00           H+0
HETATM   46  H   UNK     0       3.198  -0.061  -1.687  0.00  0.00           H+0
HETATM   47  H   UNK     0       1.604   0.733  -4.167  0.00  0.00           H+0
HETATM   48  H   UNK     0       1.756   4.798  -3.712  0.00  0.00           H+0
HETATM   49  H   UNK     0       0.446   4.505  -0.718  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.193   4.742  -0.649  0.00  0.00           H+0
HETATM   51  H   UNK     0       2.539   2.790   0.646  0.00  0.00           H+0
HETATM   52  H   UNK     0       1.105   3.534   1.327  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.273   2.062  -0.222  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    5    3   11    1                                             
CONECT    3    2    4   27   28                                             
CONECT    4    3   29                                                       
CONECT    5    6    2   30   31                                             
CONECT    6    5    7   32   33                                             
CONECT    7    6    8   34   35                                             
CONECT    8   23    9    7   11                                             
CONECT    9    8   10   36   37                                             
CONECT   10    9   38                                                       
CONECT   11   12    2   39    8                                             
CONECT   12   11   13   40   41                                             
CONECT   13   12   14   42   43                                             
CONECT   14   16   15   13   23                                             
CONECT   15   14   44   45   46                                             
CONECT   16   14   20   17                                                  
CONECT   17   16   18   47                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   48                                                  
CONECT   20   21   16   19                                                  
CONECT   21   20   22   49   50                                             
CONECT   22   21   23   51   52                                             
CONECT   23    8   14   53   22                                             
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    3                                                            
CONECT   28    3                                                            
CONECT   29    4                                                            
CONECT   30    5                                                            
CONECT   31    5                                                            
CONECT   32    6                                                            
CONECT   33    6                                                            
CONECT   34    7                                                            
CONECT   35    7                                                            
CONECT   36    9                                                            
CONECT   37    9                                                            
CONECT   38   10                                                            
CONECT   39   11                                                            
CONECT   40   12                                                            
CONECT   41   12                                                            
CONECT   42   13                                                            
CONECT   43   13                                                            
CONECT   44   15                                                            
CONECT   45   15                                                            
CONECT   46   15                                                            
CONECT   47   17                                                            
CONECT   48   19                                                            
CONECT   49   21                                                            
CONECT   50   21                                                            
CONECT   51   22                                                            
CONECT   52   22                                                            
CONECT   53   23                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  112    0
END

RDKit          3D

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M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₃

Average Mass

318.4570 Da

Monoisotopic Mass

318.21949 Da

IUPAC Name

[(1S,2S,6S,7S,10R)-6-(hydroxymethyl)-6,10-dimethyl-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-11,14-dien-2-yl]methanol

Traditional Name

[(1S,2S,6S,7S,10R)-6-(hydroxymethyl)-6,10-dimethyl-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-11,14-dien-2-yl]methanol

CAS Registry Number

Not Available

SMILES

[H]OC([H])([H])[C@@]1(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])[C@]2(C([H])([H])O[H])[C@@]3([H])C([H])([H])C([H])([H])C4=C([H])OC([H])=C4[C@]3(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]12[H]

InChI Identifier

InChI=1S/C20H30O3/c1-18(12-21)7-3-8-20(13-22)16(18)6-9-19(2)15-11-23-10-14(15)4-5-17(19)20/h10-11,16-17,21-22H,3-9,12-13H2,1-2H3/t16-,17-,18+,19-,20+/m0/s1

InChI Key

HJTMHDSGDBNZJV-UHZRXMQZSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Spongia sp.	JEOL database	Carroll, A. R., et al, J. Nat. Prod. 71, 884 (2008)

Chemical Taxonomy

Classification

Not classified

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	3.42	ALOGPS
logP	3.19	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	15.09	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	53.6 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	90.57 m³·mol⁻¹	ChemAxon
Polarizability	36.39 Å³	ChemAxon
Number of Rings	4	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

24715433

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24878745

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Carroll, A. R., et al. (2008). Carroll, A. R., et al, J. Nat. Prod. 71, 884 (2008) . J. Nat. Prod..

Showing NP-Card for 19,20-dihydroxyspongia-13(16),14-diene (NP0033783)

MOL for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)

3D MOL for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)

3D SDF for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)

3D-SDF for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)

PDB for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)

3D PDB for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)

SMILES for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)

INCHI for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)

Structure for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)

3D Structure for NP0033783 (19,20-dihydroxyspongia-13(16),14-diene)