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 23:45:27 UTC

Update Date

2021-09-26 23:18:09 UTC

HMDB ID

HMDB0260190

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene

Description

(8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene belongs to the class of organic compounds known as pregnane steroids. These are steroids with a structure based on the 21-carbon pregnane skeleton. Based on a literature review very few articles have been published on (8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene. This compound has been identified in human blood as reported by (PMID: 31557052 ). (8s,9s,10r,13r,14s,17s)-17-ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3h-cyclopenta[a]phenanthrene is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene 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

HMDB0260190
     RDKit          3D
(8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17...
 55 58  0  0  0  0  0  0  0  0999 V2000
    5.5184    0.9184    0.5253 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3044    1.1246   -0.3570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1378    0.4742    0.3252 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3114   -0.9927    0.5523 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8406   -1.3917    0.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2490   -0.7743   -0.5067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2181   -0.8684   -0.5782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6918   -1.9196    0.3939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1709   -1.9302    0.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6607   -0.5488    0.9799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1198   -0.5692    1.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0147   -0.7226    0.1373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3223   -0.7525   -1.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1018   -0.2765   -1.3718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3927    0.3314   -0.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9612    1.7226   -0.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9397    0.4393   -0.4430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2665    1.2848    0.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0649    1.6876    0.0048 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8664    0.5609   -0.5181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3519    0.8719   -1.9418 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3423    1.6173    0.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122    1.0865    1.5954 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8333   -0.1480    0.4842 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1073    2.2264   -0.3570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.7177   -1.3377 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9761    0.9582    1.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7416   -1.5126   -0.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8177   -1.2387    1.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5253   -0.8504    1.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7401   -2.4707    0.7978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7282   -1.3848   -1.3305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5049   -1.2630   -1.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4211   -2.9166   -0.0653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2016   -1.8907    1.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3914   -2.5914    1.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6633   -2.3494   -0.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0904   -0.2461    1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2682   -1.4194    2.0463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3689    0.3471    1.9109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7404    0.1290    0.1315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6542   -1.6353    0.2694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8323   -1.1927   -2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6357   -0.3290   -2.3676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9385    1.9855    1.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4134    2.4449   -0.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0199    1.7278   -0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7924    0.9818   -1.4242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1949    0.8294    1.5843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8721    2.2334    0.6762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5845    2.2931    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8411    2.3937   -0.8212 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8949    1.8205   -1.9928 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4333    0.9724   -2.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9038    0.0053   -2.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20  3  1  0
 20  6  1  0
 17  7  1  0
 15 10  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 14 44  1  0
 16 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
M  END


  Mrv1652309122101452D          

 21 24  0  0  0  0            999 V2000
    6.1111   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -0.9107    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  3  7  1  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
  6 11  1  0  0  0  0
 11 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
 10 15  1  0  0  0  0
 15 16  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
 14 19  1  0  0  0  0
 15 20  1  0  0  0  0
  7 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0260190

> <DATABASE_NAME>
hmdb

> <SMILES>
CCC1CCC2C3CCC4CCC=CC4(C)C3CCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C21H34/c1-4-15-9-11-18-17-10-8-16-7-5-6-13-20(16,2)19(17)12-14-21(15,18)3/h6,13,15-19H,4-5,7-12,14H2,1-3H3

> <INCHI_KEY>
HOWBJCLELHJALU-UHFFFAOYSA-N

> <FORMULA>
C21H34

> <MOLECULAR_WEIGHT>
286.503

> <EXACT_MASS>
286.266051095

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
36.737827686656495

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-ethyl-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-ene

> <ALOGPS_LOGP>
6.76

> <JCHEM_LOGP>
6.190952529666667

> <ALOGPS_LOGS>
-7.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
91.7124

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.34e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-ethyl-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-ene

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0260190
     RDKit          3D
(8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17...
 55 58  0  0  0  0  0  0  0  0999 V2000
    5.5184    0.9184    0.5253 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3044    1.1246   -0.3570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1378    0.4742    0.3252 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3114   -0.9927    0.5523 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8406   -1.3917    0.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2490   -0.7743   -0.5067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2181   -0.8684   -0.5782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6918   -1.9196    0.3939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1709   -1.9302    0.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6607   -0.5488    0.9799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1198   -0.5692    1.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0147   -0.7226    0.1373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3223   -0.7525   -1.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1018   -0.2765   -1.3718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3927    0.3314   -0.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9612    1.7226   -0.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9397    0.4393   -0.4430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2665    1.2848    0.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0649    1.6876    0.0048 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8664    0.5609   -0.5181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3519    0.8719   -1.9418 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3423    1.6173    0.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122    1.0865    1.5954 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8333   -0.1480    0.4842 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1073    2.2264   -0.3570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.7177   -1.3377 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9761    0.9582    1.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7416   -1.5126   -0.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8177   -1.2387    1.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5253   -0.8504    1.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7401   -2.4707    0.7978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7282   -1.3848   -1.3305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5049   -1.2630   -1.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4211   -2.9166   -0.0653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2016   -1.8907    1.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3914   -2.5914    1.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6633   -2.3494   -0.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0904   -0.2461    1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2682   -1.4194    2.0463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3689    0.3471    1.9109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7404    0.1290    0.1315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6542   -1.6353    0.2694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8323   -1.1927   -2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6357   -0.3290   -2.3676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9385    1.9855    1.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4134    2.4449   -0.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0199    1.7278   -0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7924    0.9818   -1.4242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1949    0.8294    1.5843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8721    2.2334    0.6762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5845    2.2931    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8411    2.3937   -0.8212 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8949    1.8205   -1.9928 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4333    0.9724   -2.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9038    0.0053   -2.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20  3  1  0
 20  6  1  0
 17  7  1  0
 15 10  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 14 44  1  0
 16 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
M  END

HEADER    PROTEIN                                 12-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-21         0                                  
HETATM    1  C   UNK     0      11.407  -1.269   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.882  -1.480   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.937  -0.264   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.365   1.215   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.090   2.079   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.874   1.134   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.398  -0.314   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.405  -1.492   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.889  -1.221   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.366   0.228   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.358   1.405   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.835   2.854   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.319   3.125   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.326   1.947   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.850   0.499   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.857  -0.678   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.341  -0.407   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.182   1.041   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.810   2.218   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.373  -0.949   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.069  -1.700   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    7                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    3    8   21                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10    6   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   10   16   20                                             
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20   15                                                            
CONECT   21    7                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   48    0
END

COMPND    HMDB0260190
HETATM    1  C1  UNL     1       5.518   0.918   0.525  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.304   1.125  -0.357  1.00  0.00           C  
HETATM    3  C3  UNL     1       3.138   0.474   0.325  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.311  -0.993   0.552  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.841  -1.392   0.768  1.00  0.00           C  
HETATM    6  C6  UNL     1       1.249  -0.774  -0.507  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.218  -0.868  -0.578  1.00  0.00           C  
HETATM    8  C8  UNL     1      -0.692  -1.920   0.394  1.00  0.00           C  
HETATM    9  C9  UNL     1      -2.171  -1.930   0.596  1.00  0.00           C  
HETATM   10  C10 UNL     1      -2.661  -0.549   0.980  1.00  0.00           C  
HETATM   11  C11 UNL     1      -4.120  -0.569   1.317  1.00  0.00           C  
HETATM   12  C12 UNL     1      -5.015  -0.723   0.137  1.00  0.00           C  
HETATM   13  C13 UNL     1      -4.322  -0.752  -1.155  1.00  0.00           C  
HETATM   14  C14 UNL     1      -3.102  -0.277  -1.372  1.00  0.00           C  
HETATM   15  C15 UNL     1      -2.393   0.331  -0.206  1.00  0.00           C  
HETATM   16  C16 UNL     1      -2.961   1.723  -0.032  1.00  0.00           C  
HETATM   17  C17 UNL     1      -0.940   0.439  -0.443  1.00  0.00           C  
HETATM   18  C18 UNL     1      -0.267   1.285   0.599  1.00  0.00           C  
HETATM   19  C19 UNL     1       1.065   1.688   0.005  1.00  0.00           C  
HETATM   20  C20 UNL     1       1.866   0.561  -0.518  1.00  0.00           C  
HETATM   21  C21 UNL     1       2.352   0.872  -1.942  1.00  0.00           C  
HETATM   22  H1  UNL     1       6.342   1.617   0.284  1.00  0.00           H  
HETATM   23  H2  UNL     1       5.212   1.086   1.595  1.00  0.00           H  
HETATM   24  H3  UNL     1       5.833  -0.148   0.484  1.00  0.00           H  
HETATM   25  H4  UNL     1       4.107   2.226  -0.357  1.00  0.00           H  
HETATM   26  H5  UNL     1       4.537   0.718  -1.338  1.00  0.00           H  
HETATM   27  H6  UNL     1       2.976   0.958   1.309  1.00  0.00           H  
HETATM   28  H7  UNL     1       3.742  -1.513  -0.313  1.00  0.00           H  
HETATM   29  H8  UNL     1       3.818  -1.239   1.507  1.00  0.00           H  
HETATM   30  H9  UNL     1       1.525  -0.850   1.670  1.00  0.00           H  
HETATM   31  H10 UNL     1       1.740  -2.471   0.798  1.00  0.00           H  
HETATM   32  H11 UNL     1       1.728  -1.385  -1.331  1.00  0.00           H  
HETATM   33  H12 UNL     1      -0.505  -1.263  -1.600  1.00  0.00           H  
HETATM   34  H13 UNL     1      -0.421  -2.917  -0.065  1.00  0.00           H  
HETATM   35  H14 UNL     1      -0.202  -1.891   1.365  1.00  0.00           H  
HETATM   36  H15 UNL     1      -2.391  -2.591   1.457  1.00  0.00           H  
HETATM   37  H16 UNL     1      -2.663  -2.349  -0.279  1.00  0.00           H  
HETATM   38  H17 UNL     1      -2.090  -0.246   1.880  1.00  0.00           H  
HETATM   39  H18 UNL     1      -4.268  -1.419   2.046  1.00  0.00           H  
HETATM   40  H19 UNL     1      -4.369   0.347   1.911  1.00  0.00           H  
HETATM   41  H20 UNL     1      -5.740   0.129   0.131  1.00  0.00           H  
HETATM   42  H21 UNL     1      -5.654  -1.635   0.269  1.00  0.00           H  
HETATM   43  H22 UNL     1      -4.832  -1.193  -2.004  1.00  0.00           H  
HETATM   44  H23 UNL     1      -2.636  -0.329  -2.368  1.00  0.00           H  
HETATM   45  H24 UNL     1      -2.938   1.986   1.032  1.00  0.00           H  
HETATM   46  H25 UNL     1      -2.413   2.445  -0.681  1.00  0.00           H  
HETATM   47  H26 UNL     1      -4.020   1.728  -0.362  1.00  0.00           H  
HETATM   48  H27 UNL     1      -0.792   0.982  -1.424  1.00  0.00           H  
HETATM   49  H28 UNL     1      -0.195   0.829   1.584  1.00  0.00           H  
HETATM   50  H29 UNL     1      -0.872   2.233   0.676  1.00  0.00           H  
HETATM   51  H30 UNL     1       1.585   2.293   0.788  1.00  0.00           H  
HETATM   52  H31 UNL     1       0.841   2.394  -0.821  1.00  0.00           H  
HETATM   53  H32 UNL     1       2.895   1.820  -1.993  1.00  0.00           H  
HETATM   54  H33 UNL     1       1.433   0.972  -2.584  1.00  0.00           H  
HETATM   55  H34 UNL     1       2.904   0.005  -2.360  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3   25   26
CONECT    3    4   20   27
CONECT    4    5   28   29
CONECT    5    6   30   31
CONECT    6    7   20   32
CONECT    7    8   17   33
CONECT    8    9   34   35
CONECT    9   10   36   37
CONECT   10   11   15   38
CONECT   11   12   39   40
CONECT   12   13   41   42
CONECT   13   14   14   43
CONECT   14   15   44
CONECT   15   16   17
CONECT   16   45   46   47
CONECT   17   18   48
CONECT   18   19   49   50
CONECT   19   20   51   52
CONECT   20   21
CONECT   21   53   54   55
END

HMDB0260190
     RDKit          3D
(8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17...
 55 58  0  0  0  0  0  0  0  0999 V2000
    5.5184    0.9184    0.5253 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3044    1.1246   -0.3570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1378    0.4742    0.3252 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3114   -0.9927    0.5523 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8406   -1.3917    0.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2490   -0.7743   -0.5067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2181   -0.8684   -0.5782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6918   -1.9196    0.3939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1709   -1.9302    0.5965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6607   -0.5488    0.9799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1198   -0.5692    1.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0147   -0.7226    0.1373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3223   -0.7525   -1.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1018   -0.2765   -1.3718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3927    0.3314   -0.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9612    1.7226   -0.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9397    0.4393   -0.4430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2665    1.2848    0.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0649    1.6876    0.0048 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8664    0.5609   -0.5181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3519    0.8719   -1.9418 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3423    1.6173    0.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122    1.0865    1.5954 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8333   -0.1480    0.4842 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1073    2.2264   -0.3570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.7177   -1.3377 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9761    0.9582    1.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7416   -1.5126   -0.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8177   -1.2387    1.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5253   -0.8504    1.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7401   -2.4707    0.7978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7282   -1.3848   -1.3305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5049   -1.2630   -1.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4211   -2.9166   -0.0653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2016   -1.8907    1.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3914   -2.5914    1.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6633   -2.3494   -0.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0904   -0.2461    1.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2682   -1.4194    2.0463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3689    0.3471    1.9109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7404    0.1290    0.1315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6542   -1.6353    0.2694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8323   -1.1927   -2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6357   -0.3290   -2.3676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9385    1.9855    1.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4134    2.4449   -0.6809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0199    1.7278   -0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7924    0.9818   -1.4242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1949    0.8294    1.5843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8721    2.2334    0.6762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5845    2.2931    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8411    2.3937   -0.8212 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8949    1.8205   -1.9928 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4333    0.9724   -2.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9038    0.0053   -2.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20  3  1  0
 20  6  1  0
 17  7  1  0
 15 10  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 14 44  1  0
 16 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₁H₃₄

Average Molecular Weight

286.503

Monoisotopic Molecular Weight

286.266051095

IUPAC Name

14-ethyl-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-ene

Traditional Name

14-ethyl-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-ene

CAS Registry Number

Not Available

SMILES

CCC1CCC2C3CCC4CCC=CC4(C)C3CCC12C

InChI Identifier

InChI=1S/C21H34/c1-4-15-9-11-18-17-10-8-16-7-5-6-13-20(16,2)19(17)12-14-21(15,18)3/h6,13,15-19H,4-5,7-12,14H2,1-3H3

InChI Key

HOWBJCLELHJALU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pregnane steroids. These are steroids with a structure based on the 21-carbon pregnane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Pregnane steroids

Direct Parent

Pregnane steroids

Alternative Parents

Substituents

Pregnane-skeleton
Delta-1-steroid
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Hydrocarbon
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic 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	6.76	ALOGPS
logP	6.19	ChemAxon
logS	-7.3	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	91.71 m³·mol⁻¹	ChemAxon
Polarizability	36.74 Å³	ChemAxon
Number of Rings	4	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]+	176.253	32859911
AllCCS	[M+H-H2O]+	173.087	32859911
AllCCS	[M+Na]+	180.031	32859911
AllCCS	[M+NH4]+	179.188	32859911
AllCCS	[M-H]-	184.124	32859911
AllCCS	[M+Na-2H]-	184.486	32859911
AllCCS	[M+HCOO]-	185.024	32859911
DeepCCS	[M-2H]-	206.481	30932474
DeepCCS	[M+Na]+	181.82	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene	CCC1CCC2C3CCC4CCC=CC4(C)C3CCC12C	2513.9	Standard polar	33892256
(8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene	CCC1CCC2C3CCC4CCC=CC4(C)C3CCC12C	2305.2	Standard non polar	33892256
(8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene	CCC1CCC2C3CCC4CCC=CC4(C)C3CCC12C	2257.4	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 - (8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene GC-MS (Non-derivatized) - 70eV, Positive	splash10-0ab9-0590000000-c181f3347533525ce799	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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

14474543

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

19897457

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 (8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene (HMDB0260190)

MOL for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

3D MOL for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

3D SDF for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

3D-SDF for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

PDB for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

3D PDB for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

SMILES for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

INCHI for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

Structure for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

3D Structure for HMDB0260190 ((8S,9S,10R,13R,14S,17S)-17-Ethyl-10,13-dimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthrene)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra