NP-MRD: Showing NP-Card for (13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid (NP0024149)

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Record Information

Version

2.0

Created at

2021-06-19 16:36:40 UTC

Updated at

2021-06-29 23:48:17 UTC

NP-MRD ID

NP0024149

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid

Provided By

JEOL Database JEOL Logo

Description

(13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid is found in Hymenaea courbaril. (13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid was first documented in 2002 (Abdel-Kader, M., et al.). Based on a literature review very few articles have been published on CHEMBL463535.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192118363D          

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     RDKit          3D

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  Mrv1652306192118363D          

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    0.7143   -3.9831    2.5277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -4.0538    1.7730 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4713   -4.9013    1.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0744   -3.9089   -2.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1444   -1.4563    1.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3314   -2.1716    3.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1734   -1.2900    3.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6726   -0.1781    3.3448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4077    0.0195    4.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8385    2.0428    3.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0306    0.9925    2.8908 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4922    2.6795    2.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2738    1.6153    4.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
 23  8  1  0  0  0  0
  6  3  1  0  0  0  0
 12 14  1  0  0  0  0
  3  4  1  0  0  0  0
  3  2  1  0  0  0  0
 10 20  1  0  0  0  0
  2  1  2  3  0  0  0
 10  8  1  0  0  0  0
 15 16  1  0  0  0  0
 20 21  1  0  0  0  0
  8  9  1  6  0  0  0
 12 11  1  0  0  0  0
 23 24  1  0  0  0  0
 14 15  1  0  0  0  0
  3  5  1  1  0  0  0
 15 20  1  0  0  0  0
 15 17  1  6  0  0  0
 10 11  2  0  0  0  0
 20 46  1  1  0  0  0
 21 22  1  0  0  0  0
 17 19  1  0  0  0  0
  8  7  1  0  0  0  0
 17 18  2  0  0  0  0
 22 23  1  0  0  0  0
 12 13  2  0  0  0  0
 21 47  1  0  0  0  0
 21 48  1  0  0  0  0
 22 49  1  0  0  0  0
 22 50  1  0  0  0  0
 23 51  1  1  0  0  0
 14 40  1  0  0  0  0
 14 41  1  0  0  0  0
 11 39  1  0  0  0  0
  7 34  1  0  0  0  0
  7 35  1  0  0  0  0
  6 32  1  0  0  0  0
  6 33  1  0  0  0  0
  4 28  1  0  0  0  0
  4 29  1  0  0  0  0
  4 30  1  0  0  0  0
  2 27  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
 16 42  1  0  0  0  0
 16 43  1  0  0  0  0
 16 44  1  0  0  0  0
  9 36  1  0  0  0  0
  9 37  1  0  0  0  0
  9 38  1  0  0  0  0
 24 52  1  0  0  0  0
 24 53  1  0  0  0  0
 24 54  1  0  0  0  0
  5 31  1  0  0  0  0
 19 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0024149

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)[C@@]1(C([H])([H])[H])C([H])([H])C(=O)C([H])=C2[C@]1([H])C([H])([H])C([H])([H])[C@@]([H])(C([H])([H])[H])[C@]2(C([H])([H])[H])C([H])([H])C([H])([H])[C@@](O[H])(C([H])=C([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O4/c1-6-18(3,24)9-10-19(4)13(2)7-8-15-16(19)11-14(21)12-20(15,5)17(22)23/h6,11,13,15,24H,1,7-10,12H2,2-5H3,(H,22,23)/t13-,15+,18+,19+,20+/m1/s1

> <INCHI_KEY>
WRUUAUYSSLTCMP-DDYJPHFUSA-N

> <FORMULA>
C20H30O4

> <MOLECULAR_WEIGHT>
334.456

> <EXACT_MASS>
334.214409446

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
37.235226071260286

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,5S,6R,8aS)-5-[(3R)-3-hydroxy-3-methylpent-4-en-1-yl]-1,5,6-trimethyl-3-oxo-1,2,3,5,6,7,8,8a-octahydronaphthalene-1-carboxylic acid

> <ALOGPS_LOGP>
3.15

> <JCHEM_LOGP>
3.6187059526666663

> <ALOGPS_LOGS>
-4.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.27075230258966

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.554693003874918

> <JCHEM_PKA_STRONGEST_BASIC>
-1.368086169327591

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
94.48609999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.19e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,5S,6R,8aS)-5-[(3R)-3-hydroxy-3-methylpent-4-en-1-yl]-1,5,6-trimethyl-3-oxo-6,7,8,8a-tetrahydro-2H-naphthalene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
   -5.4594    0.8886    0.2532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5009    1.2329   -0.6191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3803    0.3468   -1.1205 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5109    0.1759   -2.6380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4933   -0.9507   -0.5327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9965    0.9394   -0.7705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7532    1.1003    0.7466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2438    1.1532    1.1736 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3511    2.4408    0.5426 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4951   -0.1421    0.7592 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.1579   -0.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3655   -1.3951   -0.2639 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3062   -1.3748   -1.0530 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0236   -2.6140    0.5546 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5057   -2.7310    0.7365 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1819   -3.9830    1.5709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1706   -2.9461   -0.6272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1898   -2.4096   -1.0355 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4511   -3.8630   -1.3930 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0635   -1.4267    1.3842 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1105   -1.3077    2.9088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5882   -0.0532    3.4508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1508    1.2530    2.7478 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2433    1.6517    3.2683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4985   -0.1086    0.6822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2251    1.5958    0.5525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5163    2.2463   -1.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7334   -0.4936   -3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4707   -0.2854   -2.9001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4325    1.1329   -3.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7205   -1.4757   -0.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2300    0.2831   -1.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8782    1.9154   -1.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2737    0.3031    1.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2457    2.0259    1.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2672    2.4379   -0.5496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1732    3.3309    0.9095 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4137    2.5703    0.7721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0039    0.7238   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4349   -3.4936    0.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5378   -2.5275    1.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7143   -3.9831    2.5277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -4.0538    1.7730 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4713   -4.9013    1.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0744   -3.9089   -2.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1444   -1.4563    1.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3314   -2.1716    3.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1734   -1.2900    3.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6726   -0.1781    3.3448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4077    0.0195    4.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8385    2.0428    3.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0306    0.9925    2.8908 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4922    2.6795    2.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2738    1.6153    4.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
 23  8  1  0
  6  3  1  0
 12 14  1  0
  3  4  1  0
  3  2  1  0
 10 20  1  0
  2  1  2  3
 10  8  1  0
 15 16  1  0
 20 21  1  0
  8  9  1  6
 12 11  1  0
 23 24  1  0
 14 15  1  0
  3  5  1  1
 15 20  1  0
 15 17  1  6
 10 11  2  0
 20 46  1  1
 21 22  1  0
 17 19  1  0
  8  7  1  0
 17 18  2  0
 22 23  1  0
 12 13  2  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  1
 14 40  1  0
 14 41  1  0
 11 39  1  0
  7 34  1  0
  7 35  1  0
  6 32  1  0
  6 33  1  0
  4 28  1  0
  4 29  1  0
  4 30  1  0
  2 27  1  0
  1 25  1  0
  1 26  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
 24 52  1  0
 24 53  1  0
 24 54  1  0
  5 31  1  0
 19 45  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -5.459   0.889   0.253  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.501   1.233  -0.619  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.380   0.347  -1.121  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.511   0.176  -2.638  0.00  0.00           C+0
HETATM    5  O   UNK     0      -3.493  -0.951  -0.533  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.996   0.939  -0.771  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.753   1.100   0.747  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.244   1.153   1.174  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.351   2.441   0.543  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.495  -0.142   0.759  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.584  -0.158  -0.033  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.365  -1.395  -0.264  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.306  -1.375  -1.053  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.024  -2.614   0.555  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.506  -2.731   0.737  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.182  -3.983   1.571  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.171  -2.946  -0.627  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.190  -2.410  -1.036  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.451  -3.863  -1.393  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.064  -1.427   1.384  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.111  -1.308   2.909  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.588  -0.053   3.451  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.151   1.253   2.748  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.243   1.652   3.268  0.00  0.00           C+0
HETATM   25  H   UNK     0      -5.498  -0.109   0.682  0.00  0.00           H+0
HETATM   26  H   UNK     0      -6.225   1.596   0.553  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.516   2.246  -1.016  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.733  -0.494  -3.024  0.00  0.00           H+0
HETATM   29  H   UNK     0      -4.471  -0.285  -2.900  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.433   1.133  -3.165  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.720  -1.476  -0.831  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.230   0.283  -1.196  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.878   1.915  -1.258  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.274   0.303   1.284  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.246   2.026   1.076  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.267   2.438  -0.550  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.173   3.331   0.910  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.414   2.570   0.772  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.004   0.724  -0.502  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.435  -3.494   0.045  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.538  -2.527   1.519  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.714  -3.983   2.528  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.893  -4.054   1.773  0.00  0.00           H+0
HETATM   44  H   UNK     0       0.471  -4.901   1.046  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.074  -3.909  -2.220  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.144  -1.456   1.206  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.331  -2.172   3.417  0.00  0.00           H+0
HETATM   48  H   UNK     0       1.173  -1.290   3.178  0.00  0.00           H+0
HETATM   49  H   UNK     0      -1.673  -0.178   3.345  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.408   0.020   4.531  0.00  0.00           H+0
HETATM   51  H   UNK     0      -0.839   2.043   3.082  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.031   0.993   2.891  0.00  0.00           H+0
HETATM   53  H   UNK     0       1.492   2.680   2.987  0.00  0.00           H+0
HETATM   54  H   UNK     0       1.274   1.615   4.363  0.00  0.00           H+0
CONECT    1    2   25   26                                                  
CONECT    2    3    1   27                                                  
CONECT    3    6    4    2    5                                             
CONECT    4    3   28   29   30                                             
CONECT    5    3   31                                                       
CONECT    6    7    3   32   33                                             
CONECT    7    6    8   34   35                                             
CONECT    8   23   10    9    7                                             
CONECT    9    8   36   37   38                                             
CONECT   10   20    8   11                                                  
CONECT   11   12   10   39                                                  
CONECT   12   14   11   13                                                  
CONECT   13   12                                                            
CONECT   14   12   15   40   41                                             
CONECT   15   16   14   20   17                                             
CONECT   16   15   42   43   44                                             
CONECT   17   15   19   18                                                  
CONECT   18   17                                                            
CONECT   19   17   45                                                       
CONECT   20   10   21   15   46                                             
CONECT   21   20   22   47   48                                             
CONECT   22   21   23   49   50                                             
CONECT   23    8   24   22   51                                             
CONECT   24   23   52   53   54                                             
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    2                                                            
CONECT   28    4                                                            
CONECT   29    4                                                            
CONECT   30    4                                                            
CONECT   31    5                                                            
CONECT   32    6                                                            
CONECT   33    6                                                            
CONECT   34    7                                                            
CONECT   35    7                                                            
CONECT   36    9                                                            
CONECT   37    9                                                            
CONECT   38    9                                                            
CONECT   39   11                                                            
CONECT   40   14                                                            
CONECT   41   14                                                            
CONECT   42   16                                                            
CONECT   43   16                                                            
CONECT   44   16                                                            
CONECT   45   19                                                            
CONECT   46   20                                                            
CONECT   47   21                                                            
CONECT   48   21                                                            
CONECT   49   22                                                            
CONECT   50   22                                                            
CONECT   51   23                                                            
CONECT   52   24                                                            
CONECT   53   24                                                            
CONECT   54   24                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  110    0
END

RDKit          3D

54 55  0  0  0  0  0  0  0  0999 V2000
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   -4.5009    1.2329   -0.6191 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2438    1.1532    1.1736 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3511    2.4408    0.5426 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4951   -0.1421    0.7592 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.1579   -0.0331 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0635   -1.4267    1.3842 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1105   -1.3077    2.9088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5882   -0.0532    3.4508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1508    1.2530    2.7478 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2433    1.6517    3.2683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4985   -0.1086    0.6822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2251    1.5958    0.5525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5163    2.2463   -1.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7334   -0.4936   -3.0240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4707   -0.2854   -2.9001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4325    1.1329   -3.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7205   -1.4757   -0.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2300    0.2831   -1.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8782    1.9154   -1.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2737    0.3031    1.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2457    2.0259    1.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2672    2.4379   -0.5496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1732    3.3309    0.9095 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4137    2.5703    0.7721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0039    0.7238   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4349   -3.4936    0.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5378   -2.5275    1.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7143   -3.9831    2.5277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8931   -4.0538    1.7730 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4713   -4.9013    1.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0744   -3.9089   -2.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1444   -1.4563    1.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3314   -2.1716    3.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1734   -1.2900    3.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6726   -0.1781    3.3448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4077    0.0195    4.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8385    2.0428    3.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0306    0.9925    2.8908 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4922    2.6795    2.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2738    1.6153    4.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
 23  8  1  0
  6  3  1  0
 12 14  1  0
  3  4  1  0
  3  2  1  0
 10 20  1  0
  2  1  2  3
 10  8  1  0
 15 16  1  0
 20 21  1  0
  8  9  1  6
 12 11  1  0
 23 24  1  0
 14 15  1  0
  3  5  1  1
 15 20  1  0
 15 17  1  6
 10 11  2  0
 20 46  1  1
 21 22  1  0
 17 19  1  0
  8  7  1  0
 17 18  2  0
 22 23  1  0
 12 13  2  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  1
 14 40  1  0
 14 41  1  0
 11 39  1  0
  7 34  1  0
  7 35  1  0
  6 32  1  0
  6 33  1  0
  4 28  1  0
  4 29  1  0
  4 30  1  0
  2 27  1  0
  1 25  1  0
  1 26  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
 24 52  1  0
 24 53  1  0
 24 54  1  0
  5 31  1  0
 19 45  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₄

Average Mass

334.4560 Da

Monoisotopic Mass

334.21441 Da

IUPAC Name

(1S,5S,6R,8aS)-5-[(3R)-3-hydroxy-3-methylpent-4-en-1-yl]-1,5,6-trimethyl-3-oxo-1,2,3,5,6,7,8,8a-octahydronaphthalene-1-carboxylic acid

Traditional Name

(1S,5S,6R,8aS)-5-[(3R)-3-hydroxy-3-methylpent-4-en-1-yl]-1,5,6-trimethyl-3-oxo-6,7,8,8a-tetrahydro-2H-naphthalene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

[H]OC(=O)[C@@]1(C([H])([H])[H])C([H])([H])C(=O)C([H])=C2[C@]1([H])C([H])([H])C([H])([H])[C@@]([H])(C([H])([H])[H])[C@]2(C([H])([H])[H])C([H])([H])C([H])([H])[C@@](O[H])(C([H])=C([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H30O4/c1-6-18(3,24)9-10-19(4)13(2)7-8-15-16(19)11-14(21)12-20(15,5)17(22)23/h6,11,13,15,24H,1,7-10,12H2,2-5H3,(H,22,23)/t13-,15+,18+,19+,20+/m1/s1

InChI Key

WRUUAUYSSLTCMP-DDYJPHFUSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, 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
Hymenaea courbaril	JEOL database	Abdel-Kader, M., et al, J. Nat. Prod. 65, 11 (2002)

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	3.15	ALOGPS
logP	3.62	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	4.55	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	94.49 m³·mol⁻¹	ChemAxon
Polarizability	37.24 Å³	ChemAxon
Number of Rings	2	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

9100925

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10925680

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Abdel-Kader, M., et al. (2002). Abdel-Kader, M., et al, J. Nat. Prod. 65, 11 (2002). J. Nat. Prod..

Showing NP-Card for (13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid (NP0024149)

MOL for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)

3D MOL for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)

3D SDF for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)

3D-SDF for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)

PDB for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)

3D PDB for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)

SMILES for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)

INCHI for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)

Structure for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)

3D Structure for NP0024149 ((13R)-2-oxo-13-hydroxy-1(10),14-ent-halimadien-18-oic acid)