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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 12:34:25 UTC

Update Date

2021-09-26 23:07:08 UTC

HMDB ID

HMDB0253725

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one

Description

(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. Based on a literature review very few articles have been published on (5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one. This compound has been identified in human blood as reported by (PMID: 31557052 ). (5alpha,17beta)-17-benzoyl-4-azaandrost-1-en-3-one is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one 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

  Mrv1652309112114342D          

 28 32  0  0  0  0            999 V2000
    4.3228   -0.9107    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
    3.6826    0.6076    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
    5.0168    0.6509    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
    5.2939   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830   -1.5571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1111   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4220    0.0841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2392    0.1970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7456   -0.4543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4347   -1.2185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6175   -1.3314    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
   -0.9098    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 N   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
  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
  2  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
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
  6 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
  5 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 21 27  1  0  0  0  0
 22 28  1  0  0  0  0
M  END

HMDB0253725
     RDKit          3D
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one
 59 63  0  0  0  0  0  0  0  0999 V2000
    3.8372    0.0452    2.1472 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2545    0.1159    0.7367 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2245   -0.5885   -0.1434 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2589    0.0224   -0.7125 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4640    1.4445   -0.4730 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4330    2.0836   -0.9879 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5204    2.1048    0.3759 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1719    1.5792    0.3844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5930    1.8197   -0.9889 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7858    0.6524   -1.4962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9949    0.1099   -0.3331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9416   -0.5998    0.6385 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2217   -0.7594    1.9222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2998   -0.7146    1.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7991   -1.2802    0.5348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7348   -2.8227    0.7014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2077   -0.9743    0.2197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7174    0.3688    0.3854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0203    1.3414    0.6930 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1436    0.5978    0.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6876    1.8678    0.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0196    2.1414    0.0886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8891    1.1018   -0.2034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3975   -0.1811   -0.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0393   -0.4168   -0.1197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2995   -1.2217   -1.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0207   -0.5063   -1.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0242   -0.8961   -0.7098 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4004    0.8152    2.8042 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9151    0.2922    2.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7861   -0.9719    2.5639 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1305   -1.6595   -0.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9596   -0.5151   -1.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8351    2.9259    0.9460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5914    2.0909    1.1863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8744    2.6769   -0.8774 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3360    2.1077   -1.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3844   -0.1201   -1.9760 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0619    1.0495   -2.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6187    0.9826    0.2270 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0899   -1.6335    0.2069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4863    0.1133    2.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5716   -1.6621    2.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6971    0.2607    2.0762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6478   -1.4076    2.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2204   -3.1836    0.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8654   -3.0978    1.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5523   -3.3021    0.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9004   -1.7519    0.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0328    2.7125    0.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4246    3.1394    0.1662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9347    1.2658   -0.3508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0839   -0.9994   -0.5379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7231   -1.4318   -0.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1357   -0.6502   -1.7591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2922   -2.2889   -1.4806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1847    0.5604   -1.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7320   -0.9360   -2.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5441   -1.8167   -1.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  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  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 17 26  1  0
 26 27  1  0
 27 28  1  0
  8  2  1  0
 28 11  1  0
 12  2  1  0
 28 15  1  0
 25 20  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  4 33  1  0
  7 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 21 50  1  0
 22 51  1  0
 23 52  1  0
 24 53  1  0
 25 54  1  0
 26 55  1  0
 26 56  1  0
 27 57  1  0
 27 58  1  0
 28 59  1  0
M  END

  Mrv1652309112114342D          

 28 32  0  0  0  0            999 V2000
    4.3228   -0.9107    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
    3.6826    0.6076    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
    5.0168    0.6509    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
    5.2939   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830   -1.5571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1111   -0.6800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4220    0.0841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2392    0.1970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7456   -0.4543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4347   -1.2185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6175   -1.3314    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
   -0.9098    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 N   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
  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
  2  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
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
  6 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
  5 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 21 27  1  0  0  0  0
 22 28  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0253725

> <DATABASE_NAME>
hmdb

> <SMILES>
CC12CCC3C(CCC4NC(=O)C=CC34C)C1CCC2C(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H31NO2/c1-24-14-12-19-17(8-11-21-25(19,2)15-13-22(27)26-21)18(24)9-10-20(24)23(28)16-6-4-3-5-7-16/h3-7,13,15,17-21H,8-12,14H2,1-2H3,(H,26,27)

> <INCHI_KEY>
ZYTQEOWFSVTRLX-UHFFFAOYSA-N

> <FORMULA>
C25H31NO2

> <MOLECULAR_WEIGHT>
377.528

> <EXACT_MASS>
377.235479242

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
43.334905920347

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14-benzoyl-2,15-dimethyl-6-azatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-5-one

> <ALOGPS_LOGP>
4.27

> <JCHEM_LOGP>
4.357057972000001

> <ALOGPS_LOGS>
-5.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.746134514864117

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.399283918663446

> <JCHEM_PKA_STRONGEST_BASIC>
-0.1641307537344524

> <JCHEM_POLAR_SURFACE_AREA>
46.17

> <JCHEM_REFRACTIVITY>
111.4886

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.74e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-benzoyl-2,15-dimethyl-6-azatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0253725
     RDKit          3D
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one
 59 63  0  0  0  0  0  0  0  0999 V2000
    3.8372    0.0452    2.1472 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2545    0.1159    0.7367 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2245   -0.5885   -0.1434 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2589    0.0224   -0.7125 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4640    1.4445   -0.4730 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4330    2.0836   -0.9879 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5204    2.1048    0.3759 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1719    1.5792    0.3844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5930    1.8197   -0.9889 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7858    0.6524   -1.4962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9949    0.1099   -0.3331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9416   -0.5998    0.6385 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2217   -0.7594    1.9222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2998   -0.7146    1.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7991   -1.2802    0.5348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7348   -2.8227    0.7014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2077   -0.9743    0.2197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7174    0.3688    0.3854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0203    1.3414    0.6930 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1436    0.5978    0.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6876    1.8678    0.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0196    2.1414    0.0886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8891    1.1018   -0.2034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3975   -0.1811   -0.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0393   -0.4168   -0.1197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2995   -1.2217   -1.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0207   -0.5063   -1.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0242   -0.8961   -0.7098 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4004    0.8152    2.8042 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9151    0.2922    2.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7861   -0.9719    2.5639 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1305   -1.6595   -0.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9596   -0.5151   -1.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8351    2.9259    0.9460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5914    2.0909    1.1863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8744    2.6769   -0.8774 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3360    2.1077   -1.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3844   -0.1201   -1.9760 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0619    1.0495   -2.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6187    0.9826    0.2270 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0899   -1.6335    0.2069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4863    0.1133    2.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5716   -1.6621    2.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6971    0.2607    2.0762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6478   -1.4076    2.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2204   -3.1836    0.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8654   -3.0978    1.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5523   -3.3021    0.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9004   -1.7519    0.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0328    2.7125    0.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4246    3.1394    0.1662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9347    1.2658   -0.3508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0839   -0.9994   -0.5379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7231   -1.4318   -0.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1357   -0.6502   -1.7591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2922   -2.2889   -1.4806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1847    0.5604   -1.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7320   -0.9360   -2.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5441   -1.8167   -1.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  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  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 17 26  1  0
 26 27  1  0
 27 28  1  0
  8  2  1  0
 28 11  1  0
 12  2  1  0
 28 15  1  0
 25 20  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  4 33  1  0
  7 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 21 50  1  0
 22 51  1  0
 23 52  1  0
 24 53  1  0
 25 54  1  0
 26 55  1  0
 26 56  1  0
 27 57  1  0
 27 58  1  0
 28 59  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       8.069  -1.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.398  -0.314   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.405  -1.492   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.889  -1.221   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.366   0.228   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.358   1.405   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.874   1.134   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.090   2.079   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.365   1.215   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.937  -0.264   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.882  -1.480   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.302  -2.907   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      11.407  -1.269   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.988   0.157   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.513   0.368   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.458  -0.848   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.878  -2.275   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.353  -2.485   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.835   2.854   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.319   3.125   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.326   1.947   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.850   0.499   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.857  -0.678   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.341  -0.407   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.182   1.041   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.698   1.312   0.000  0.00  0.00           O+0
HETATM   27  N   UNK     0       0.810   2.218   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       3.373  -0.949   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7   10                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7   19                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    2   11                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
CONECT   19    6   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21    5   23   28                                             
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   21                                                       
CONECT   28   22                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

COMPND    HMDB0253725
HETATM    1  C1  UNL     1       3.837   0.045   2.147  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.255   0.116   0.737  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.225  -0.589  -0.143  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.259   0.022  -0.713  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.464   1.445  -0.473  1.00  0.00           C  
HETATM    6  O1  UNL     1       6.433   2.084  -0.988  1.00  0.00           O  
HETATM    7  N1  UNL     1       4.520   2.105   0.376  1.00  0.00           N  
HETATM    8  C6  UNL     1       3.172   1.579   0.384  1.00  0.00           C  
HETATM    9  C7  UNL     1       2.593   1.820  -0.989  1.00  0.00           C  
HETATM   10  C8  UNL     1       1.786   0.652  -1.496  1.00  0.00           C  
HETATM   11  C9  UNL     1       0.995   0.110  -0.333  1.00  0.00           C  
HETATM   12  C10 UNL     1       1.942  -0.600   0.638  1.00  0.00           C  
HETATM   13  C11 UNL     1       1.222  -0.759   1.922  1.00  0.00           C  
HETATM   14  C12 UNL     1      -0.300  -0.715   1.797  1.00  0.00           C  
HETATM   15  C13 UNL     1      -0.799  -1.280   0.535  1.00  0.00           C  
HETATM   16  C14 UNL     1      -0.735  -2.823   0.701  1.00  0.00           C  
HETATM   17  C15 UNL     1      -2.208  -0.974   0.220  1.00  0.00           C  
HETATM   18  C16 UNL     1      -2.717   0.369   0.385  1.00  0.00           C  
HETATM   19  O2  UNL     1      -2.020   1.341   0.693  1.00  0.00           O  
HETATM   20  C17 UNL     1      -4.144   0.598   0.173  1.00  0.00           C  
HETATM   21  C18 UNL     1      -4.688   1.868   0.267  1.00  0.00           C  
HETATM   22  C19 UNL     1      -6.020   2.141   0.089  1.00  0.00           C  
HETATM   23  C20 UNL     1      -6.889   1.102  -0.203  1.00  0.00           C  
HETATM   24  C21 UNL     1      -6.397  -0.181  -0.308  1.00  0.00           C  
HETATM   25  C22 UNL     1      -5.039  -0.417  -0.120  1.00  0.00           C  
HETATM   26  C23 UNL     1      -2.300  -1.222  -1.327  1.00  0.00           C  
HETATM   27  C24 UNL     1      -1.021  -0.506  -1.742  1.00  0.00           C  
HETATM   28  C25 UNL     1      -0.024  -0.896  -0.710  1.00  0.00           C  
HETATM   29  H1  UNL     1       3.400   0.815   2.804  1.00  0.00           H  
HETATM   30  H2  UNL     1       4.915   0.292   2.042  1.00  0.00           H  
HETATM   31  H3  UNL     1       3.786  -0.972   2.564  1.00  0.00           H  
HETATM   32  H4  UNL     1       4.131  -1.660  -0.367  1.00  0.00           H  
HETATM   33  H5  UNL     1       5.960  -0.515  -1.356  1.00  0.00           H  
HETATM   34  H6  UNL     1       4.835   2.926   0.946  1.00  0.00           H  
HETATM   35  H7  UNL     1       2.591   2.091   1.186  1.00  0.00           H  
HETATM   36  H8  UNL     1       1.874   2.677  -0.877  1.00  0.00           H  
HETATM   37  H9  UNL     1       3.336   2.108  -1.739  1.00  0.00           H  
HETATM   38  H10 UNL     1       2.384  -0.120  -1.976  1.00  0.00           H  
HETATM   39  H11 UNL     1       1.062   1.050  -2.234  1.00  0.00           H  
HETATM   40  H12 UNL     1       0.619   0.983   0.227  1.00  0.00           H  
HETATM   41  H13 UNL     1       2.090  -1.634   0.207  1.00  0.00           H  
HETATM   42  H14 UNL     1       1.486   0.113   2.575  1.00  0.00           H  
HETATM   43  H15 UNL     1       1.572  -1.662   2.474  1.00  0.00           H  
HETATM   44  H16 UNL     1      -0.697   0.261   2.076  1.00  0.00           H  
HETATM   45  H17 UNL     1      -0.648  -1.408   2.632  1.00  0.00           H  
HETATM   46  H18 UNL     1       0.220  -3.184   0.264  1.00  0.00           H  
HETATM   47  H19 UNL     1      -0.865  -3.098   1.762  1.00  0.00           H  
HETATM   48  H20 UNL     1      -1.552  -3.302   0.132  1.00  0.00           H  
HETATM   49  H21 UNL     1      -2.900  -1.752   0.643  1.00  0.00           H  
HETATM   50  H22 UNL     1      -4.033   2.713   0.496  1.00  0.00           H  
HETATM   51  H23 UNL     1      -6.425   3.139   0.166  1.00  0.00           H  
HETATM   52  H24 UNL     1      -7.935   1.266  -0.351  1.00  0.00           H  
HETATM   53  H25 UNL     1      -7.084  -0.999  -0.538  1.00  0.00           H  
HETATM   54  H26 UNL     1      -4.723  -1.432  -0.207  1.00  0.00           H  
HETATM   55  H27 UNL     1      -3.136  -0.650  -1.759  1.00  0.00           H  
HETATM   56  H28 UNL     1      -2.292  -2.289  -1.481  1.00  0.00           H  
HETATM   57  H29 UNL     1      -1.185   0.560  -1.874  1.00  0.00           H  
HETATM   58  H30 UNL     1      -0.732  -0.936  -2.729  1.00  0.00           H  
HETATM   59  H31 UNL     1       0.544  -1.817  -1.048  1.00  0.00           H  
CONECT    1    2   29   30   31
CONECT    2    3    8   12
CONECT    3    4    4   32
CONECT    4    5   33
CONECT    5    6    6    7
CONECT    7    8   34
CONECT    8    9   35
CONECT    9   10   36   37
CONECT   10   11   38   39
CONECT   11   12   28   40
CONECT   12   13   41
CONECT   13   14   42   43
CONECT   14   15   44   45
CONECT   15   16   17   28
CONECT   16   46   47   48
CONECT   17   18   26   49
CONECT   18   19   19   20
CONECT   20   21   21   25
CONECT   21   22   50
CONECT   22   23   23   51
CONECT   23   24   52
CONECT   24   25   25   53
CONECT   25   54
CONECT   26   27   55   56
CONECT   27   28   57   58
CONECT   28   59
END

HMDB0253725
     RDKit          3D
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one
 59 63  0  0  0  0  0  0  0  0999 V2000
    3.8372    0.0452    2.1472 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2545    0.1159    0.7367 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2245   -0.5885   -0.1434 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2589    0.0224   -0.7125 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4640    1.4445   -0.4730 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4330    2.0836   -0.9879 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5204    2.1048    0.3759 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1719    1.5792    0.3844 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5930    1.8197   -0.9889 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7858    0.6524   -1.4962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9949    0.1099   -0.3331 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9416   -0.5998    0.6385 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2217   -0.7594    1.9222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2998   -0.7146    1.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7991   -1.2802    0.5348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7348   -2.8227    0.7014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2077   -0.9743    0.2197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7174    0.3688    0.3854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0203    1.3414    0.6930 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1436    0.5978    0.1726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6876    1.8678    0.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.8891    1.1018   -0.2034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3975   -0.1811   -0.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2995   -1.2217   -1.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0207   -0.5063   -1.7415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0242   -0.8961   -0.7098 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4004    0.8152    2.8042 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9151    0.2922    2.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7861   -0.9719    2.5639 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1305   -1.6595   -0.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9596   -0.5151   -1.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8351    2.9259    0.9460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5914    2.0909    1.1863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8744    2.6769   -0.8774 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0619    1.0495   -2.2344 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6187    0.9826    0.2270 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0899   -1.6335    0.2069 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4863    0.1133    2.5752 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5716   -1.6621    2.4744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6971    0.2607    2.0762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6478   -1.4076    2.6324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2204   -3.1836    0.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8654   -3.0978    1.7616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5523   -3.3021    0.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9004   -1.7519    0.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0328    2.7125    0.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4246    3.1394    0.1662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9347    1.2658   -0.3508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0839   -0.9994   -0.5379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7231   -1.4318   -0.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1357   -0.6502   -1.7591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2922   -2.2889   -1.4806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1847    0.5604   -1.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7320   -0.9360   -2.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5441   -1.8167   -1.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
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 27 58  1  0
 28 59  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(5a,17b)-17-Benzoyl-4-azaandrost-1-en-3-one	Generator
(5Α,17β)-17-benzoyl-4-azaandrost-1-en-3-one	Generator

Chemical Formula

C₂₅H₃₁NO₂

Average Molecular Weight

377.528

Monoisotopic Molecular Weight

377.235479242

IUPAC Name

14-benzoyl-2,15-dimethyl-6-azatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-5-one

Traditional Name

14-benzoyl-2,15-dimethyl-6-azatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-en-5-one

CAS Registry Number

Not Available

SMILES

CC12CCC3C(CCC4NC(=O)C=CC34C)C1CCC2C(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C25H31NO2/c1-24-14-12-19-17(8-11-21-25(19,2)15-13-22(27)26-21)18(24)9-10-20(24)23(28)16-6-4-3-5-7-16/h3-7,13,15,17-21H,8-12,14H2,1-2H3,(H,26,27)

InChI Key

ZYTQEOWFSVTRLX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Androstane steroids

Direct Parent

Androgens and derivatives

Alternative Parents

Substituents

Androgen-skeleton
3-hydroxysteroid
Hydroxysteroid
4-azasteroid
Azasteroid
Alkyl-phenylketone
Phenylketone
Benzoyl
Aryl alkyl ketone
Aryl ketone
Monocyclic benzene moiety
Benzenoid
Cyclic carboximidic acid
Ketone
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	4.27	ALOGPS
logP	4.36	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	14.4	ChemAxon
pKa (Strongest Basic)	-0.16	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.17 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	111.49 m³·mol⁻¹	ChemAxon
Polarizability	43.33 Å³	ChemAxon
Number of Rings	5	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
DeepCCS	[M-2H]-	227.883	30932474
DeepCCS	[M+Na]+	204.174	30932474
AllCCS	[M+H]+	198.3	32859911
AllCCS	[M+H-H2O]+	195.6	32859911
AllCCS	[M+NH4]+	200.8	32859911
AllCCS	[M+Na]+	201.5	32859911
AllCCS	[M-H]-	201.5	32859911
AllCCS	[M+Na-2H]-	202.0	32859911
AllCCS	[M+HCOO]-	202.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one	CC12CCC3C(CCC4NC(=O)C=CC34C)C1CCC2C(=O)C1=CC=CC=C1	4427.1	Standard polar	33892256
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one	CC12CCC3C(CCC4NC(=O)C=CC34C)C1CCC2C(=O)C1=CC=CC=C1	3060.6	Standard non polar	33892256
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one	CC12CCC3C(CCC4NC(=O)C=CC34C)C1CCC2C(=O)C1=CC=CC=C1	3689.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one,1TMS,isomer #1	CC12C=CC(=O)N([Si](C)(C)C)C1CCC1C2CCC2(C)C(C(=O)C3=CC=CC=C3)CCC12	3394.5	Semi standard non polar	33892256
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one,1TMS,isomer #1	CC12C=CC(=O)N([Si](C)(C)C)C1CCC1C2CCC2(C)C(C(=O)C3=CC=CC=C3)CCC12	3312.8	Standard non polar	33892256
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one,1TMS,isomer #1	CC12C=CC(=O)N([Si](C)(C)C)C1CCC1C2CCC2(C)C(C(=O)C3=CC=CC=C3)CCC12	3775.7	Standard polar	33892256
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one,1TBDMS,isomer #1	CC12C=CC(=O)N([Si](C)(C)C(C)(C)C)C1CCC1C2CCC2(C)C(C(=O)C3=CC=CC=C3)CCC12	3623.1	Semi standard non polar	33892256
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one,1TBDMS,isomer #1	CC12C=CC(=O)N([Si](C)(C)C(C)(C)C)C1CCC1C2CCC2(C)C(C(=O)C3=CC=CC=C3)CCC12	3532.9	Standard non polar	33892256
(5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one,1TBDMS,isomer #1	CC12C=CC(=O)N([Si](C)(C)C(C)(C)C)C1CCC1C2CCC2(C)C(C(=O)C3=CC=CC=C3)CCC12	3908.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-2975000000-9b144105810c7691d578	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one 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

13743971

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

18795642

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 (5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one (HMDB0253725)

MOL for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

3D MOL for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

3D SDF for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

3D-SDF for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

PDB for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

3D PDB for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

SMILES for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

INCHI for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

Structure for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

3D Structure for HMDB0253725 ((5alpha,17beta)-17-Benzoyl-4-azaandrost-1-en-3-one)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra