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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 23:43:25 UTC

Update Date

2021-09-26 23:18:08 UTC

HMDB ID

HMDB0260173

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol

Description

(8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol belongs to the class of organic compounds known as pregnane-type alkaloids. These are alkaloids with a structure based on the pregnane skeleton, which is characterized by the presence of monomethylamino or dimethylamino substituents either at C-3 and/or at the C-20 position in basic steroidal skeleton. Based on a literature review very few articles have been published on (8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol. This compound has been identified in human blood as reported by (PMID: 31557052 ). (8r,9s,10r,13s,14s,17r)-13-ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1h-cyclopenta[a]phenanthren-17-ol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol 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

  Mrv1652309122101432D          

 24 27  0  0  0  0            999 V2000
    3.8598    2.4186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228    1.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5484    1.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3093    1.6043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9089    1.7826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.1221    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901   -0.6539    0.0000 O   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
  7  8  1  0  0  0  0
  3  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
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  3  0  0  0  0
 11 14  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  6 22  1  0  0  0  0
 17 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
M  END

HMDB0260173
     RDKit          3D
(8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14...
 53 56  0  0  0  0  0  0  0  0999 V2000
   -4.2387   -2.6340   -0.8484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8545   -1.5152   -0.5878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4159   -0.1570   -0.2742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4715    0.4453    0.4089 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1210    0.5377   -1.5698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185    0.7390   -1.5807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3519    0.9476   -0.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0922    1.0364    0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7645    1.7203   -0.9548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1414    2.1166   -0.4635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8690    0.9092   -0.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1874    0.8200   -0.1866 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9373   -0.4105    0.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1339   -0.4446   -0.5828 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3246    0.2896   -1.5098 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -1.6657   -0.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6997   -1.4344   -0.3952 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2124   -0.3269    0.4892 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7514   -0.2154    0.6776 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0211   -1.4639    0.1886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4295   -1.4788    0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1202   -0.1430    0.5345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5111    0.1151    1.9663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2130    1.3615    2.2731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5707   -3.6146   -1.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0639   -0.2478    0.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5650    1.5665   -1.5580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4592   -0.0260   -2.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1694   -0.1509   -2.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3269    1.6282   -2.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8189    1.9246    0.1367 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2225    1.7977    1.0657 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1959    2.6571   -1.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7813    1.0882   -1.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6185    2.6569   -1.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0242    2.8691    0.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7273    1.6681   -0.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2593   -0.3737    1.2737 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6033   -2.2530   -0.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1919   -2.3339    0.8053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2049   -2.3931   -0.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6704   -1.0505   -1.4531 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7669   -0.4821    1.4684 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5822   -0.2748    1.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2625   -1.6985   -0.8667 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5115   -2.3009    0.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5912   -2.0534    1.4535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9019   -2.1510   -0.2791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1527   -0.7708    2.2579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6286    0.0135    2.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2988    2.1262    1.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7641    1.8837    3.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2667    1.1461    2.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0
  2  3  1  0
  3  4  1  0
  3  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  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 13 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22  3  1  0
 22  7  1  0
 19  8  1  0
 18 11  1  0
  1 25  1  0
  4 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 12 37  1  0
 13 38  1  0
 16 39  1  0
 16 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 21 48  1  0
 23 49  1  0
 23 50  1  0
 24 51  1  0
 24 52  1  0
 24 53  1  0
M  END

  Mrv1652309122101432D          

 24 27  0  0  0  0            999 V2000
    3.8598    2.4186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228    1.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5484    1.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3093    1.6043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9089    1.7826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.1221    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1901   -0.6539    0.0000 O   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
  7  8  1  0  0  0  0
  3  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
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  3  0  0  0  0
 11 14  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  6 22  1  0  0  0  0
 17 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0260173

> <DATABASE_NAME>
hmdb

> <SMILES>
CCC12CCC3C(CCC4=CC(CCC34)N=O)C1CCC2(O)C#C

> <INCHI_IDENTIFIER>
InChI=1S/C21H29NO2/c1-3-20-11-9-17-16-8-6-15(22-24)13-14(16)5-7-18(17)19(20)10-12-21(20,23)4-2/h2,13,15-19,23H,3,5-12H2,1H3

> <INCHI_KEY>
FPGXTJXAYVNDRS-UHFFFAOYSA-N

> <FORMULA>
C21H29NO2

> <MOLECULAR_WEIGHT>
327.468

> <EXACT_MASS>
327.219829178

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
38.03269604164087

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
15-ethyl-14-ethynyl-5-nitrosotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-14-ol

> <ALOGPS_LOGP>
3.76

> <JCHEM_LOGP>
3.728141032000001

> <ALOGPS_LOGS>
-4.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.926482140494574

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.90929074637612

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5103517111794575

> <JCHEM_POLAR_SURFACE_AREA>
49.660000000000004

> <JCHEM_REFRACTIVITY>
94.5012

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.04e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-ethyl-14-ethynyl-5-nitrosotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-14-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0260173
     RDKit          3D
(8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14...
 53 56  0  0  0  0  0  0  0  0999 V2000
   -4.2387   -2.6340   -0.8484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8545   -1.5152   -0.5878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4159   -0.1570   -0.2742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4715    0.4453    0.4089 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1210    0.5377   -1.5698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185    0.7390   -1.5807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3519    0.9476   -0.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0922    1.0364    0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7645    1.7203   -0.9548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1414    2.1166   -0.4635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8690    0.9092   -0.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1874    0.8200   -0.1866 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9373   -0.4105    0.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1339   -0.4446   -0.5828 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3246    0.2896   -1.5098 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -1.6657   -0.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6997   -1.4344   -0.3952 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2124   -0.3269    0.4892 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7514   -0.2154    0.6776 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0211   -1.4639    0.1886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4295   -1.4788    0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1202   -0.1430    0.5345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5111    0.1151    1.9663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2130    1.3615    2.2731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5707   -3.6146   -1.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0639   -0.2478    0.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5650    1.5665   -1.5580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4592   -0.0260   -2.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1694   -0.1509   -2.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3269    1.6282   -2.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8189    1.9246    0.1367 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2225    1.7977    1.0657 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1959    2.6571   -1.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7813    1.0882   -1.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6185    2.6569   -1.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0242    2.8691    0.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7273    1.6681   -0.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2593   -0.3737    1.2737 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6033   -2.2530   -0.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1919   -2.3339    0.8053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2049   -2.3931   -0.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6704   -1.0505   -1.4531 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7669   -0.4821    1.4684 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5822   -0.2748    1.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2625   -1.6985   -0.8667 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5115   -2.3009    0.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5912   -2.0534    1.4535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9019   -2.1510   -0.2791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1527   -0.7708    2.2579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6286    0.0135    2.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2988    2.1262    1.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7641    1.8837    3.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2667    1.1461    2.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0
  2  3  1  0
  3  4  1  0
  3  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  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 13 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22  3  1  0
 22  7  1  0
 19  8  1  0
 18 11  1  0
  1 25  1  0
  4 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 12 37  1  0
 13 38  1  0
 16 39  1  0
 16 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 21 48  1  0
 23 49  1  0
 23 50  1  0
 24 51  1  0
 24 52  1  0
 24 53  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       7.205   4.515   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.069   3.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.398   1.854   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.405   3.032   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.889   2.761   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.366   1.312   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.358   0.135   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.874   0.406   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.090  -0.539   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.365   0.325   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.937   1.804   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.357   2.399   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.777   2.995   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       9.163   3.327   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.835  -1.314   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.319  -1.585   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.182   0.499   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.341   1.947   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.857   2.218   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.850   1.041   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      -1.698   0.228   0.000  0.00  0.00           N+0
HETATM   24  O   UNK     0      -2.221  -1.221   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8   11                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8   15                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    3   12   14                                             
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11                                                            
CONECT   15    7   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    6   17                                                  
CONECT   23   19   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

COMPND    HMDB0260173
HETATM    1  C1  UNL     1      -4.239  -2.634  -0.848  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.854  -1.515  -0.588  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.416  -0.157  -0.274  1.00  0.00           C  
HETATM    4  O1  UNL     1      -4.471   0.445   0.409  1.00  0.00           O  
HETATM    5  C4  UNL     1      -3.121   0.538  -1.570  1.00  0.00           C  
HETATM    6  C5  UNL     1      -1.618   0.739  -1.581  1.00  0.00           C  
HETATM    7  C6  UNL     1      -1.352   0.948  -0.107  1.00  0.00           C  
HETATM    8  C7  UNL     1       0.092   1.036   0.237  1.00  0.00           C  
HETATM    9  C8  UNL     1       0.764   1.720  -0.955  1.00  0.00           C  
HETATM   10  C9  UNL     1       2.141   2.117  -0.464  1.00  0.00           C  
HETATM   11  C10 UNL     1       2.869   0.909  -0.070  1.00  0.00           C  
HETATM   12  C11 UNL     1       4.187   0.820  -0.187  1.00  0.00           C  
HETATM   13  C12 UNL     1       4.937  -0.411   0.212  1.00  0.00           C  
HETATM   14  N1  UNL     1       6.134  -0.445  -0.583  1.00  0.00           N  
HETATM   15  O2  UNL     1       6.325   0.290  -1.510  1.00  0.00           O  
HETATM   16  C13 UNL     1       4.166  -1.666  -0.091  1.00  0.00           C  
HETATM   17  C14 UNL     1       2.700  -1.434  -0.395  1.00  0.00           C  
HETATM   18  C15 UNL     1       2.212  -0.327   0.489  1.00  0.00           C  
HETATM   19  C16 UNL     1       0.751  -0.215   0.678  1.00  0.00           C  
HETATM   20  C17 UNL     1       0.021  -1.464   0.189  1.00  0.00           C  
HETATM   21  C18 UNL     1      -1.430  -1.479   0.500  1.00  0.00           C  
HETATM   22  C19 UNL     1      -2.120  -0.143   0.534  1.00  0.00           C  
HETATM   23  C20 UNL     1      -2.511   0.115   1.966  1.00  0.00           C  
HETATM   24  C21 UNL     1      -3.213   1.361   2.273  1.00  0.00           C  
HETATM   25  H1  UNL     1      -4.571  -3.615  -1.095  1.00  0.00           H  
HETATM   26  H2  UNL     1      -5.064  -0.248   0.836  1.00  0.00           H  
HETATM   27  H3  UNL     1      -3.565   1.566  -1.558  1.00  0.00           H  
HETATM   28  H4  UNL     1      -3.459  -0.026  -2.461  1.00  0.00           H  
HETATM   29  H5  UNL     1      -1.169  -0.151  -2.005  1.00  0.00           H  
HETATM   30  H6  UNL     1      -1.327   1.628  -2.184  1.00  0.00           H  
HETATM   31  H7  UNL     1      -1.819   1.925   0.137  1.00  0.00           H  
HETATM   32  H8  UNL     1       0.223   1.798   1.066  1.00  0.00           H  
HETATM   33  H9  UNL     1       0.196   2.657  -1.128  1.00  0.00           H  
HETATM   34  H10 UNL     1       0.781   1.088  -1.839  1.00  0.00           H  
HETATM   35  H11 UNL     1       2.619   2.657  -1.324  1.00  0.00           H  
HETATM   36  H12 UNL     1       2.024   2.869   0.338  1.00  0.00           H  
HETATM   37  H13 UNL     1       4.727   1.668  -0.583  1.00  0.00           H  
HETATM   38  H14 UNL     1       5.259  -0.374   1.274  1.00  0.00           H  
HETATM   39  H15 UNL     1       4.603  -2.253  -0.927  1.00  0.00           H  
HETATM   40  H16 UNL     1       4.192  -2.334   0.805  1.00  0.00           H  
HETATM   41  H17 UNL     1       2.205  -2.393  -0.294  1.00  0.00           H  
HETATM   42  H18 UNL     1       2.670  -1.051  -1.453  1.00  0.00           H  
HETATM   43  H19 UNL     1       2.767  -0.482   1.468  1.00  0.00           H  
HETATM   44  H20 UNL     1       0.582  -0.275   1.804  1.00  0.00           H  
HETATM   45  H21 UNL     1       0.262  -1.699  -0.867  1.00  0.00           H  
HETATM   46  H22 UNL     1       0.512  -2.301   0.776  1.00  0.00           H  
HETATM   47  H23 UNL     1      -1.591  -2.053   1.454  1.00  0.00           H  
HETATM   48  H24 UNL     1      -1.902  -2.151  -0.279  1.00  0.00           H  
HETATM   49  H25 UNL     1      -3.153  -0.771   2.258  1.00  0.00           H  
HETATM   50  H26 UNL     1      -1.629   0.014   2.664  1.00  0.00           H  
HETATM   51  H27 UNL     1      -3.299   2.126   1.513  1.00  0.00           H  
HETATM   52  H28 UNL     1      -2.764   1.884   3.171  1.00  0.00           H  
HETATM   53  H29 UNL     1      -4.267   1.146   2.623  1.00  0.00           H  
CONECT    1    2    2    2   25
CONECT    2    3
CONECT    3    4    5   22
CONECT    4   26
CONECT    5    6   27   28
CONECT    6    7   29   30
CONECT    7    8   22   31
CONECT    8    9   19   32
CONECT    9   10   33   34
CONECT   10   11   35   36
CONECT   11   12   12   18
CONECT   12   13   37
CONECT   13   14   16   38
CONECT   14   15   15
CONECT   16   17   39   40
CONECT   17   18   41   42
CONECT   18   19   43
CONECT   19   20   44
CONECT   20   21   45   46
CONECT   21   22   47   48
CONECT   22   23
CONECT   23   24   49   50
CONECT   24   51   52   53
END

HMDB0260173
     RDKit          3D
(8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14...
 53 56  0  0  0  0  0  0  0  0999 V2000
   -4.2387   -2.6340   -0.8484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8545   -1.5152   -0.5878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4159   -0.1570   -0.2742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4715    0.4453    0.4089 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1210    0.5377   -1.5698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185    0.7390   -1.5807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3519    0.9476   -0.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0922    1.0364    0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7645    1.7203   -0.9548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1414    2.1166   -0.4635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8690    0.9092   -0.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1874    0.8200   -0.1866 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9373   -0.4105    0.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1339   -0.4446   -0.5828 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3246    0.2896   -1.5098 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1659   -1.6657   -0.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6997   -1.4344   -0.3952 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2124   -0.3269    0.4892 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7514   -0.2154    0.6776 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0211   -1.4639    0.1886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4295   -1.4788    0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1202   -0.1430    0.5345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5111    0.1151    1.9663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2130    1.3615    2.2731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5707   -3.6146   -1.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0639   -0.2478    0.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5650    1.5665   -1.5580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4592   -0.0260   -2.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1694   -0.1509   -2.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3269    1.6282   -2.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8189    1.9246    0.1367 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2225    1.7977    1.0657 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1959    2.6571   -1.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7813    1.0882   -1.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6185    2.6569   -1.3239 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0242    2.8691    0.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7273    1.6681   -0.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2593   -0.3737    1.2737 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6033   -2.2530   -0.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1919   -2.3339    0.8053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2049   -2.3931   -0.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6704   -1.0505   -1.4531 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7669   -0.4821    1.4684 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5822   -0.2748    1.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2625   -1.6985   -0.8667 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5115   -2.3009    0.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5912   -2.0534    1.4535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9019   -2.1510   -0.2791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1527   -0.7708    2.2579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6286    0.0135    2.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2988    2.1262    1.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7641    1.8837    3.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2667    1.1461    2.6235 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0
  2  3  1  0
  3  4  1  0
  3  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  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 13 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22  3  1  0
 22  7  1  0
 19  8  1  0
 18 11  1  0
  1 25  1  0
  4 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  0
  6 30  1  0
  7 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 12 37  1  0
 13 38  1  0
 16 39  1  0
 16 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 21 48  1  0
 23 49  1  0
 23 50  1  0
 24 51  1  0
 24 52  1  0
 24 53  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₁H₂₉NO₂

Average Molecular Weight

327.468

Monoisotopic Molecular Weight

327.219829178

IUPAC Name

15-ethyl-14-ethynyl-5-nitrosotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-14-ol

Traditional Name

15-ethyl-14-ethynyl-5-nitrosotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-14-ol

CAS Registry Number

Not Available

SMILES

CCC12CCC3C(CCC4=CC(CCC34)N=O)C1CCC2(O)C#C

InChI Identifier

InChI=1S/C21H29NO2/c1-3-20-11-9-17-16-8-6-15(22-24)13-14(16)5-7-18(17)19(20)10-12-21(20,23)4-2/h2,13,15-19,23H,3,5-12H2,1H3

InChI Key

FPGXTJXAYVNDRS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pregnane-type alkaloids. These are alkaloids with a structure based on the pregnane skeleton, which is characterized by the presence of monomethylamino or dimethylamino substituents either at C-3 and/or at the C-20 position in basic steroidal skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal alkaloids

Direct Parent

Pregnane-type alkaloids

Alternative Parents

Substituents

Pregnane-type alkaloid
17-hydroxysteroid
Hydroxysteroid
Estrane-skeleton
Delta-4-steroid
Azasteroid
Alkaloid or derivatives
Ynone
Tertiary alcohol
Cyclic alcohol
Organic nitroso compound
Acetylide
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
C-nitroso compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Alcohol
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	3.76	ALOGPS
logP	3.73	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	17.91	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.66 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	94.5 m³·mol⁻¹	ChemAxon
Polarizability	38.03 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	184.431	32859911
AllCCS	[M+H-H2O]+	181.56	32859911
AllCCS	[M+Na]+	187.846	32859911
AllCCS	[M+NH4]+	187.085	32859911
AllCCS	[M-H]-	187.199	32859911
AllCCS	[M+Na-2H]-	187.456	32859911
AllCCS	[M+HCOO]-	187.885	32859911
DeepCCS	[M-2H]-	210.47	30932474
DeepCCS	[M+Na]+	186.035	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol	CCC12CCC3C(CCC4=CC(CCC34)N=O)C1CCC2(O)C#C	3153.2	Standard polar	33892256
(8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol	CCC12CCC3C(CCC4=CC(CCC34)N=O)C1CCC2(O)C#C	2713.5	Standard non polar	33892256
(8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol	CCC12CCC3C(CCC4=CC(CCC34)N=O)C1CCC2(O)C#C	2888.8	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 - (8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0002-0391000000-e06d1591427c9fcbda76	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-05	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146677541

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 (8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol (HMDB0260173)

MOL for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

3D MOL for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

3D SDF for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

3D-SDF for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

PDB for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

3D PDB for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

SMILES for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

INCHI for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

Structure for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

3D Structure for HMDB0260173 ((8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-3-nitroso-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra