Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 23:36:11 UTC

Update Date

2021-09-26 23:18:01 UTC

HMDB ID

HMDB0260088

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid

Description

1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Based on a literature review very few articles have been published on 1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). (1r,4as,10as)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0260088
     RDKit          3D
(1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanth...
 50 52  0  0  0  0  0  0  0  0999 V2000
    5.4254    0.2256    0.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4473    0.5749   -0.6235 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5978    2.0017   -1.0646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0343    0.2711   -0.2173 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4367    0.9311    0.8356 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1241    0.6294    1.1910 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3860   -0.3143    0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9870   -0.9751   -0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2843   -0.6781   -0.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1761   -1.9818   -1.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2480   -1.5640   -1.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9132   -1.0095   -0.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8618    0.1213   -0.5647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1307    1.3359   -1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7889   -0.3164   -1.6330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8153   -1.4573   -2.1524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7119    0.6021   -2.1097 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7338    0.3940    0.6413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9929    0.5766    1.9169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4959    0.5771    1.7272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0037   -0.5963    0.9437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8935   -1.7631    1.9406 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9505    0.3924    1.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3488    0.8063    0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7198   -0.8624    0.4211 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6893   -0.0799   -1.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2226    2.1015   -2.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6812    2.2391   -1.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0970    2.7035   -0.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0300    1.6721    1.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6997    1.1666    2.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7587   -1.1946   -1.7098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5925   -2.1362   -2.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2438   -2.9354   -0.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7822   -2.4993   -1.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2975   -0.8657   -2.2636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5991   -1.8103    0.2354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4298    2.2639   -0.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3149    1.5058   -2.1614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0206    1.1416   -1.0153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6967    0.5477   -1.9800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4222    1.2365    0.4161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3938   -0.5027    0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3017   -0.1490    2.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2610    1.5863    2.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1620    1.5632    1.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0673    0.5014    2.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7249   -1.3641    2.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0283   -2.3915    1.6683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8415   -2.3408    1.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 17  1  0
 13 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
  9  4  1  0
 21 12  1  0
 21  7  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 14 38  1  0
 14 39  1  0
 14 40  1  0
 17 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 22 48  1  0
 22 49  1  0
 22 50  1  0
M  END


  Mrv1533004171500262D          

 22 24  0  0  0  0            999 V2000
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -1.3966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1053   -0.0538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  7 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  8 22  2  0  0  0  0
  4 22  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0260088

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C1=CC=C2C(CCC3C(C)(CCCC23C)C(O)=O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O2/c1-13(2)14-6-8-16-15(12-14)7-9-17-19(16,3)10-5-11-20(17,4)18(21)22/h6,8,12-13,17H,5,7,9-11H2,1-4H3,(H,21,22)

> <INCHI_KEY>
NFWKVWVWBFBAOV-UHFFFAOYSA-N

> <FORMULA>
C20H28O2

> <MOLECULAR_WEIGHT>
300.442

> <EXACT_MASS>
300.208930142

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
35.8864679694787

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid

> <ALOGPS_LOGP>
5.45

> <JCHEM_LOGP>
5.748764728000001

> <ALOGPS_LOGS>
-5.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.545782514802334

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
89.444

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.54e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
dehydroabietic acid

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0260088
     RDKit          3D
(1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanth...
 50 52  0  0  0  0  0  0  0  0999 V2000
    5.4254    0.2256    0.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4473    0.5749   -0.6235 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5978    2.0017   -1.0646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0343    0.2711   -0.2173 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4367    0.9311    0.8356 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1241    0.6294    1.1910 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3860   -0.3143    0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9870   -0.9751   -0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2843   -0.6781   -0.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1761   -1.9818   -1.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2480   -1.5640   -1.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9132   -1.0095   -0.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8618    0.1213   -0.5647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1307    1.3359   -1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7889   -0.3164   -1.6330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8153   -1.4573   -2.1524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7119    0.6021   -2.1097 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7338    0.3940    0.6413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9929    0.5766    1.9169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4959    0.5771    1.7272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0037   -0.5963    0.9437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8935   -1.7631    1.9406 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9505    0.3924    1.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3488    0.8063    0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7198   -0.8624    0.4211 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6893   -0.0799   -1.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2226    2.1015   -2.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6812    2.2391   -1.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0970    2.7035   -0.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0300    1.6721    1.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6997    1.1666    2.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7587   -1.1946   -1.7098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5925   -2.1362   -2.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2438   -2.9354   -0.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7822   -2.4993   -1.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2975   -0.8657   -2.2636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5991   -1.8103    0.2354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4298    2.2639   -0.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3149    1.5058   -2.1614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0206    1.1416   -1.0153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6967    0.5477   -1.9800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4222    1.2365    0.4161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3938   -0.5027    0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3017   -0.1490    2.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2610    1.5863    2.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1620    1.5632    1.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0673    0.5014    2.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7249   -1.3641    2.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0283   -2.3915    1.6683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8415   -2.3408    1.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 17  1  0
 13 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
  9  4  1  0
 21 12  1  0
 21  7  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 14 38  1  0
 14 39  1  0
 14 40  1  0
 17 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 22 48  1  0
 22 49  1  0
 22 50  1  0
M  END

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.831  -2.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.883  -1.090   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.151  -2.607   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -2.063  -0.100   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   22                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   17                                                  
CONECT    8    7    9   22                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13   14   19                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    7   11   18                                             
CONECT   18   17                                                            
CONECT   19   12   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22    8    4                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

COMPND    HMDB0260088
HETATM    1  C1  UNL     1       5.425   0.226   0.476  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.447   0.575  -0.624  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.598   2.002  -1.065  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.034   0.271  -0.217  1.00  0.00           C  
HETATM    5  C5  UNL     1       2.437   0.931   0.836  1.00  0.00           C  
HETATM    6  C6  UNL     1       1.124   0.629   1.191  1.00  0.00           C  
HETATM    7  C7  UNL     1       0.386  -0.314   0.526  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.987  -0.975  -0.530  1.00  0.00           C  
HETATM    9  C9  UNL     1       2.284  -0.678  -0.882  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.176  -1.982  -1.220  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.248  -1.564  -1.381  1.00  0.00           C  
HETATM   12  C12 UNL     1      -1.913  -1.010  -0.173  1.00  0.00           C  
HETATM   13  C13 UNL     1      -2.862   0.121  -0.565  1.00  0.00           C  
HETATM   14  C14 UNL     1      -2.131   1.336  -1.059  1.00  0.00           C  
HETATM   15  C15 UNL     1      -3.789  -0.316  -1.633  1.00  0.00           C  
HETATM   16  O1  UNL     1      -3.815  -1.457  -2.152  1.00  0.00           O  
HETATM   17  O2  UNL     1      -4.712   0.602  -2.110  1.00  0.00           O  
HETATM   18  C16 UNL     1      -3.734   0.394   0.641  1.00  0.00           C  
HETATM   19  C17 UNL     1      -2.993   0.577   1.917  1.00  0.00           C  
HETATM   20  C18 UNL     1      -1.496   0.577   1.727  1.00  0.00           C  
HETATM   21  C19 UNL     1      -1.004  -0.596   0.944  1.00  0.00           C  
HETATM   22  C20 UNL     1      -0.893  -1.763   1.941  1.00  0.00           C  
HETATM   23  H1  UNL     1       4.951   0.392   1.443  1.00  0.00           H  
HETATM   24  H2  UNL     1       6.349   0.806   0.373  1.00  0.00           H  
HETATM   25  H3  UNL     1       5.720  -0.862   0.421  1.00  0.00           H  
HETATM   26  H4  UNL     1       4.689  -0.080  -1.484  1.00  0.00           H  
HETATM   27  H5  UNL     1       4.223   2.102  -2.090  1.00  0.00           H  
HETATM   28  H6  UNL     1       5.681   2.239  -1.061  1.00  0.00           H  
HETATM   29  H7  UNL     1       4.097   2.703  -0.371  1.00  0.00           H  
HETATM   30  H8  UNL     1       3.030   1.672   1.351  1.00  0.00           H  
HETATM   31  H9  UNL     1       0.700   1.167   2.019  1.00  0.00           H  
HETATM   32  H10 UNL     1       2.759  -1.195  -1.710  1.00  0.00           H  
HETATM   33  H11 UNL     1       0.593  -2.136  -2.246  1.00  0.00           H  
HETATM   34  H12 UNL     1       0.244  -2.935  -0.653  1.00  0.00           H  
HETATM   35  H13 UNL     1      -1.782  -2.499  -1.730  1.00  0.00           H  
HETATM   36  H14 UNL     1      -1.297  -0.866  -2.264  1.00  0.00           H  
HETATM   37  H15 UNL     1      -2.599  -1.810   0.235  1.00  0.00           H  
HETATM   38  H16 UNL     1      -2.430   2.264  -0.569  1.00  0.00           H  
HETATM   39  H17 UNL     1      -2.315   1.506  -2.161  1.00  0.00           H  
HETATM   40  H18 UNL     1      -1.021   1.142  -1.015  1.00  0.00           H  
HETATM   41  H19 UNL     1      -5.697   0.548  -1.980  1.00  0.00           H  
HETATM   42  H20 UNL     1      -4.422   1.237   0.416  1.00  0.00           H  
HETATM   43  H21 UNL     1      -4.394  -0.503   0.754  1.00  0.00           H  
HETATM   44  H22 UNL     1      -3.302  -0.149   2.695  1.00  0.00           H  
HETATM   45  H23 UNL     1      -3.261   1.586   2.327  1.00  0.00           H  
HETATM   46  H24 UNL     1      -1.162   1.563   1.338  1.00  0.00           H  
HETATM   47  H25 UNL     1      -1.067   0.501   2.759  1.00  0.00           H  
HETATM   48  H26 UNL     1      -0.725  -1.364   2.970  1.00  0.00           H  
HETATM   49  H27 UNL     1      -0.028  -2.391   1.668  1.00  0.00           H  
HETATM   50  H28 UNL     1      -1.842  -2.341   1.979  1.00  0.00           H  
CONECT    1    2   23   24   25
CONECT    2    3    4   26
CONECT    3   27   28   29
CONECT    4    5    5    9
CONECT    5    6   30
CONECT    6    7    7   31
CONECT    7    8   21
CONECT    8    9    9   10
CONECT    9   32
CONECT   10   11   33   34
CONECT   11   12   35   36
CONECT   12   13   21   37
CONECT   13   14   15   18
CONECT   14   38   39   40
CONECT   15   16   16   17
CONECT   17   41
CONECT   18   19   42   43
CONECT   19   20   44   45
CONECT   20   21   46   47
CONECT   21   22
CONECT   22   48   49   50
END

HMDB0260088
     RDKit          3D
(1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanth...
 50 52  0  0  0  0  0  0  0  0999 V2000
    5.4254    0.2256    0.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4473    0.5749   -0.6235 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5978    2.0017   -1.0646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0343    0.2711   -0.2173 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4367    0.9311    0.8356 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1241    0.6294    1.1910 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3860   -0.3143    0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9870   -0.9751   -0.5297 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2843   -0.6781   -0.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1761   -1.9818   -1.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2480   -1.5640   -1.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9132   -1.0095   -0.1728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8618    0.1213   -0.5647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1307    1.3359   -1.0589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7889   -0.3164   -1.6330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8153   -1.4573   -2.1524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7119    0.6021   -2.1097 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7338    0.3940    0.6413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9929    0.5766    1.9169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4959    0.5771    1.7272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0037   -0.5963    0.9437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8935   -1.7631    1.9406 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9505    0.3924    1.4425 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3488    0.8063    0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7198   -0.8624    0.4211 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6893   -0.0799   -1.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2226    2.1015   -2.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6812    2.2391   -1.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0970    2.7035   -0.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0300    1.6721    1.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6997    1.1666    2.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7587   -1.1946   -1.7098 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5925   -2.1362   -2.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2438   -2.9354   -0.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7822   -2.4993   -1.7300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2975   -0.8657   -2.2636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5991   -1.8103    0.2354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4298    2.2639   -0.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3149    1.5058   -2.1614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0206    1.1416   -1.0153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6967    0.5477   -1.9800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4222    1.2365    0.4161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3938   -0.5027    0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3017   -0.1490    2.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2610    1.5863    2.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1620    1.5632    1.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0673    0.5014    2.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7249   -1.3641    2.9696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0283   -2.3915    1.6683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8415   -2.3408    1.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 17  1  0
 13 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
  9  4  1  0
 21 12  1  0
 21  7  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  6 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 14 38  1  0
 14 39  1  0
 14 40  1  0
 17 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 22 48  1  0
 22 49  1  0
 22 50  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1,4a-Dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylate	Generator
DEHYDROABIETate	Generator

Chemical Formula

C₂₀H₂₈O₂

Average Molecular Weight

300.442

Monoisotopic Molecular Weight

300.208930142

IUPAC Name

1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid

Traditional Name

dehydroabietic acid

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC=C2C(CCC3C(C)(CCCC23C)C(O)=O)=C1

InChI Identifier

InChI=1S/C20H28O2/c1-13(2)14-6-8-16-15(12-14)7-9-17-19(16,3)10-5-11-20(17,4)18(21)22/h6,8,12-13,17H,5,7,9-11H2,1-4H3,(H,21,22)

InChI Key

NFWKVWVWBFBAOV-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Abietane diterpenoid
Phenanthrene
Hydrophenanthrene
Tetralin
Benzenoid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	5.45	ALOGPS
logP	5.75	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	4.55	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	89.44 m³·mol⁻¹	ChemAxon
Polarizability	35.89 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	174.393	32859911
AllCCS	[M+H-H2O]+	171.199	32859911
AllCCS	[M+Na]+	178.202	32859911
AllCCS	[M+NH4]+	177.352	32859911
AllCCS	[M-H]-	183.134	32859911
AllCCS	[M+Na-2H]-	183.379	32859911
AllCCS	[M+HCOO]-	183.786	32859911
DeepCCS	[M-2H]-	210.449	30932474
DeepCCS	[M+Na]+	186.014	30932474

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022.	8.36 minutes	32390414
Predicted by Siyang on May 30, 2022	19.3935 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	1.44 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2823.6 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	564.9 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	226.1 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	261.1 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	448.3 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	874.4 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	904.4 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	83.7 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1648.9 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	635.5 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1728.2 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	529.8 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	480.0 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	315.6 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	426.6 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	8.1 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid	CC(C)C1=CC=C2C(CCC3C(C)(CCCC23C)C(O)=O)=C1	3312.6	Standard polar	33892256
(1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid	CC(C)C1=CC=C2C(CCC3C(C)(CCCC23C)C(O)=O)=C1	2352.4	Standard non polar	33892256
(1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid	CC(C)C1=CC=C2C(CCC3C(C)(CCCC23C)C(O)=O)=C1	2462.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0079-0690000000-08ccb1cb18e6eba70b73	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 10V, Positive-QTOF	splash10-0ue9-0096000000-db7a242ca447b1a9cfba	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 20V, Positive-QTOF	splash10-053r-0491000000-3cd28f1ea2310a249263	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 40V, Positive-QTOF	splash10-000i-4970000000-c2d2a2ca435e882afde3	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 10V, Negative-QTOF	splash10-0002-0090000000-a3c398433e3f850fe3ff	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 20V, Negative-QTOF	splash10-0a4j-0090000000-73980b3d03515b7809f7	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 40V, Negative-QTOF	splash10-053i-0090000000-dff23cf410826060d1e6	2019-02-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

14858

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for (1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid (HMDB0260088)

MOL for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

3D MOL for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

3D SDF for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

3D-SDF for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

PDB for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

3D PDB for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

SMILES for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

INCHI for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

Structure for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

3D Structure for HMDB0260088 ((1R,4As,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra