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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (7) Show 7 proteins XML

Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2022-03-07 02:49:07 UTC

HMDB ID

HMDB0000899

Secondary Accession Numbers

HMDB0011608
HMDB00899
HMDB11608

Metabolite Identification

Common Name

Androstanedione

Description

Androstanedione 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. Thus, androstanedione is considered to be a steroid lipid molecule. Androstanedione is a very hydrophobic molecule, practically insoluble in water, and relatively neutral.

Structure

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

1561
  Mrv1652305271900032D          

 25 28  0  0  1  0            999 V2000
    7.1353    1.7956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6498   -1.7578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6697   -0.0648    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3842   -0.4772    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9191   -0.4829    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0985   -0.0648    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0985    0.7601    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9125   -1.3421    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6697    0.7601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3974   -1.3363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3842    1.1725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6566   -1.7717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8790   -0.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1546   -0.0176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8790    1.0115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9254    0.3420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1409   -1.7956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3604    0.3477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0985    1.5850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3726   -0.4531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3657   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2413    0.2652    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9581   -0.8028    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1683   -0.7210    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9150   -2.0020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1 15  2  0  0  0  0
  2 21  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  3  9  1  0  0  0  0
  3 22  1  6  0  0  0
  4  6  1  0  0  0  0
  4 10  1  0  0  0  0
  4 23  1  1  0  0  0
  5  8  1  0  0  0  0
  5 14  1  0  0  0  0
  5 16  1  1  0  0  0
  6  7  1  0  0  0  0
  6 13  1  0  0  0  0
  6 24  1  6  0  0  0
  7 11  1  0  0  0  0
  7 15  1  0  0  0  0
  7 19  1  1  0  0  0
  8 12  1  0  0  0  0
  8 17  1  0  0  0  0
  8 25  1  6  0  0  0
  9 11  1  0  0  0  0
 10 12  1  0  0  0  0
 13 18  1  0  0  0  0
 14 20  1  0  0  0  0
 15 18  1  0  0  0  0
 17 21  1  0  0  0  0
 20 21  1  0  0  0  0
M  END

HMDB0000899
     RDKit          3D
Androstanedione
 49 52  0  0  0  0  0  0  0  0999 V2000
    2.7485   -0.6092   -1.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6175   -0.7646   -0.0668 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8505   -1.9608    0.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3948   -1.8210    0.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2109   -0.5271    0.5011 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6336    0.6518    0.0142 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0828    1.9601    0.4624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3825    2.1096    0.3822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1835    0.8741    0.6083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5922    1.1470    0.1171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3946   -0.0747   -0.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6152    0.0396    0.0333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8391   -1.4166   -0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475   -1.5325    0.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5819   -0.3500   -0.0637 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5924   -0.0836   -1.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9857    0.4525    0.5870 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9781    1.5149    0.3298 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3135    0.7971    0.4224 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9804   -0.6707    0.5147 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7003   -1.5294    0.9692 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1704   -1.4367   -2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4899    0.3844   -1.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8153   -0.7905   -1.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2212   -2.8340   -0.2602 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0972   -2.2317    1.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2250   -1.9557   -1.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1283   -2.6407    0.6594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2922   -0.4706    1.6097 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6402    0.5712   -1.0931 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5496    2.7551   -0.1891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4819    2.1930    1.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6985    2.8542    1.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7367    2.5841   -0.5793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2806    0.6187    1.7015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0954    1.7988    0.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936    1.7037   -0.8542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8460   -1.7244   -1.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4520   -2.2067    0.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0254   -2.4899   -0.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5329   -1.5368    1.4128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6807   -0.0903   -1.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618    0.9631   -1.7229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0372   -0.8160   -2.1379 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9108    0.2299    1.6610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9737    2.2925    1.1342 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8505    2.0202   -0.6479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9021    1.1338    1.2957 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8877    0.9148   -0.5142 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  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  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
  6 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 17  2  1  0
 20  2  1  0
 15  5  1  0
 15  9  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  1
  6 30  1  6
  7 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  1
 10 36  1  0
 10 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  0
 14 41  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  1
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
M  END

1561
  Mrv1652305271900032D          

 25 28  0  0  1  0            999 V2000
    7.1353    1.7956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6498   -1.7578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6697   -0.0648    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3842   -0.4772    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9191   -0.4829    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0985   -0.0648    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0985    0.7601    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9125   -1.3421    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6697    0.7601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3974   -1.3363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3842    1.1725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6566   -1.7717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8790   -0.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1546   -0.0176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8790    1.0115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9254    0.3420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1409   -1.7956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3604    0.3477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0985    1.5850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3726   -0.4531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3657   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2413    0.2652    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9581   -0.8028    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1683   -0.7210    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9150   -2.0020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1 15  2  0  0  0  0
  2 21  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  3  9  1  0  0  0  0
  3 22  1  6  0  0  0
  4  6  1  0  0  0  0
  4 10  1  0  0  0  0
  4 23  1  1  0  0  0
  5  8  1  0  0  0  0
  5 14  1  0  0  0  0
  5 16  1  1  0  0  0
  6  7  1  0  0  0  0
  6 13  1  0  0  0  0
  6 24  1  6  0  0  0
  7 11  1  0  0  0  0
  7 15  1  0  0  0  0
  7 19  1  1  0  0  0
  8 12  1  0  0  0  0
  8 17  1  0  0  0  0
  8 25  1  6  0  0  0
  9 11  1  0  0  0  0
 10 12  1  0  0  0  0
 13 18  1  0  0  0  0
 14 20  1  0  0  0  0
 15 18  1  0  0  0  0
 17 21  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0000899

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])CC(=O)CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12,14-16H,3-11H2,1-2H3/t12-,14-,15-,16-,18-,19-/m0/s1

> <INCHI_KEY>
RAJWOBJTTGJROA-WZNAKSSCSA-N

> <FORMULA>
C19H28O2

> <MOLECULAR_WEIGHT>
288.4244

> <EXACT_MASS>
288.20893014

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
33.826012044347785

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,7S,10R,11S,15S)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-5,14-dione

> <ALOGPS_LOGP>
3.40

> <JCHEM_LOGP>
3.9747853383333336

> <ALOGPS_LOGS>
-4.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.776207883092308

> <JCHEM_PKA_STRONGEST_BASIC>
-7.108868634299542

> <JCHEM_POLAR_SURFACE_AREA>
34.14

> <JCHEM_REFRACTIVITY>
82.7808

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.39e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,7S,10R,11S,15S)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-5,14-dione

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0000899
     RDKit          3D
Androstanedione
 49 52  0  0  0  0  0  0  0  0999 V2000
    2.7485   -0.6092   -1.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6175   -0.7646   -0.0668 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8505   -1.9608    0.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3948   -1.8210    0.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2109   -0.5271    0.5011 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6336    0.6518    0.0142 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0828    1.9601    0.4624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3825    2.1096    0.3822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1835    0.8741    0.6083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5922    1.1470    0.1171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3946   -0.0747   -0.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6152    0.0396    0.0333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8391   -1.4166   -0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475   -1.5325    0.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5819   -0.3500   -0.0637 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5924   -0.0836   -1.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9857    0.4525    0.5870 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9781    1.5149    0.3298 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3135    0.7971    0.4224 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9804   -0.6707    0.5147 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7003   -1.5294    0.9692 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1704   -1.4367   -2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4899    0.3844   -1.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8153   -0.7905   -1.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2212   -2.8340   -0.2602 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0972   -2.2317    1.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2250   -1.9557   -1.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1283   -2.6407    0.6594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2922   -0.4706    1.6097 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6402    0.5712   -1.0931 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5496    2.7551   -0.1891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4819    2.1930    1.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6985    2.8542    1.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7367    2.5841   -0.5793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2806    0.6187    1.7015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0954    1.7988    0.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936    1.7037   -0.8542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8460   -1.7244   -1.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4520   -2.2067    0.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0254   -2.4899   -0.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5329   -1.5368    1.4128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6807   -0.0903   -1.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618    0.9631   -1.7229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0372   -0.8160   -2.1379 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9108    0.2299    1.6610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9737    2.2925    1.1342 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8505    2.0202   -0.6479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9021    1.1338    1.2957 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8877    0.9148   -0.5142 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  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  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
  6 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 17  2  1  0
 20  2  1  0
 15  5  1  0
 15  9  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  1
  6 30  1  6
  7 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  1
 10 36  1  0
 10 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  0
 14 41  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  1
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
M  END

HEADER    PROTEIN                                 27-MAY-19   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: 1561                                              
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-MAY-19         0                                  
HETATM    1  O   UNK     0      13.319   3.352   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0       3.080  -3.281   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.717  -0.121   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.051  -0.891   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.316  -0.901   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.384  -0.121   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.384   1.419   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.303  -2.505   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.717   1.419   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.075  -2.494   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.051   2.189   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.692  -3.307   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.841  -0.590   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.889  -0.033   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.841   1.888   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.327   0.638   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.863  -3.352   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.739   0.649   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.384   2.959   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.429  -0.846   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.416  -2.516   0.000  0.00  0.00           C+0
HETATM   22  H   UNK     0       9.784   0.495   0.000  0.00  0.00           H+0
HETATM   23  H   UNK     0      11.122  -1.499   0.000  0.00  0.00           H+0
HETATM   24  H   UNK     0      11.514  -1.346   0.000  0.00  0.00           H+0
HETATM   25  H   UNK     0       7.308  -3.737   0.000  0.00  0.00           H+0
CONECT    1   15                                                            
CONECT    2   21                                                            
CONECT    3    4    5    9   22                                             
CONECT    4    3    6   10   23                                             
CONECT    5    3    8   14   16                                             
CONECT    6    4    7   13   24                                             
CONECT    7    6   11   15   19                                             
CONECT    8    5   12   17   25                                             
CONECT    9    3   11                                                       
CONECT   10    4   12                                                       
CONECT   11    7    9                                                       
CONECT   12    8   10                                                       
CONECT   13    6   18                                                       
CONECT   14    5   20                                                       
CONECT   15    1    7   18                                                  
CONECT   16    5                                                            
CONECT   17    8   21                                                       
CONECT   18   13   15                                                       
CONECT   19    7                                                            
CONECT   20   14   21                                                       
CONECT   21    2   17   20                                                  
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    6                                                            
CONECT   25    8                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

COMPND    HMDB0000899
HETATM    1  C1  UNL     1       2.749  -0.609  -1.559  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.618  -0.765  -0.067  1.00  0.00           C  
HETATM    3  C3  UNL     1       1.850  -1.961   0.353  1.00  0.00           C  
HETATM    4  C4  UNL     1       0.395  -1.821   0.084  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.211  -0.527   0.501  1.00  0.00           C  
HETATM    6  C6  UNL     1       0.634   0.652   0.014  1.00  0.00           C  
HETATM    7  C7  UNL     1       0.083   1.960   0.462  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.383   2.110   0.382  1.00  0.00           C  
HETATM    9  C9  UNL     1      -2.183   0.874   0.608  1.00  0.00           C  
HETATM   10  C10 UNL     1      -3.592   1.147   0.117  1.00  0.00           C  
HETATM   11  C11 UNL     1      -4.395  -0.075  -0.032  1.00  0.00           C  
HETATM   12  O1  UNL     1      -5.615   0.040   0.033  1.00  0.00           O  
HETATM   13  C12 UNL     1      -3.839  -1.417  -0.253  1.00  0.00           C  
HETATM   14  C13 UNL     1      -2.448  -1.532   0.298  1.00  0.00           C  
HETATM   15  C14 UNL     1      -1.582  -0.350  -0.064  1.00  0.00           C  
HETATM   16  C15 UNL     1      -1.592  -0.084  -1.550  1.00  0.00           C  
HETATM   17  C16 UNL     1       1.986   0.453   0.587  1.00  0.00           C  
HETATM   18  C17 UNL     1       2.978   1.515   0.330  1.00  0.00           C  
HETATM   19  C18 UNL     1       4.313   0.797   0.422  1.00  0.00           C  
HETATM   20  C19 UNL     1       3.980  -0.671   0.515  1.00  0.00           C  
HETATM   21  O2  UNL     1       4.700  -1.529   0.969  1.00  0.00           O  
HETATM   22  H1  UNL     1       2.170  -1.437  -2.039  1.00  0.00           H  
HETATM   23  H2  UNL     1       2.490   0.384  -1.933  1.00  0.00           H  
HETATM   24  H3  UNL     1       3.815  -0.791  -1.885  1.00  0.00           H  
HETATM   25  H4  UNL     1       2.221  -2.834  -0.260  1.00  0.00           H  
HETATM   26  H5  UNL     1       2.097  -2.232   1.402  1.00  0.00           H  
HETATM   27  H6  UNL     1       0.225  -1.956  -1.011  1.00  0.00           H  
HETATM   28  H7  UNL     1      -0.128  -2.641   0.659  1.00  0.00           H  
HETATM   29  H8  UNL     1      -0.292  -0.471   1.610  1.00  0.00           H  
HETATM   30  H9  UNL     1       0.640   0.571  -1.093  1.00  0.00           H  
HETATM   31  H10 UNL     1       0.550   2.755  -0.189  1.00  0.00           H  
HETATM   32  H11 UNL     1       0.482   2.193   1.490  1.00  0.00           H  
HETATM   33  H12 UNL     1      -1.699   2.854   1.172  1.00  0.00           H  
HETATM   34  H13 UNL     1      -1.737   2.584  -0.579  1.00  0.00           H  
HETATM   35  H14 UNL     1      -2.281   0.619   1.702  1.00  0.00           H  
HETATM   36  H15 UNL     1      -4.095   1.799   0.865  1.00  0.00           H  
HETATM   37  H16 UNL     1      -3.594   1.704  -0.854  1.00  0.00           H  
HETATM   38  H17 UNL     1      -3.846  -1.724  -1.322  1.00  0.00           H  
HETATM   39  H18 UNL     1      -4.452  -2.207   0.272  1.00  0.00           H  
HETATM   40  H19 UNL     1      -2.025  -2.490  -0.075  1.00  0.00           H  
HETATM   41  H20 UNL     1      -2.533  -1.537   1.413  1.00  0.00           H  
HETATM   42  H21 UNL     1      -2.681  -0.090  -1.852  1.00  0.00           H  
HETATM   43  H22 UNL     1      -1.262   0.963  -1.723  1.00  0.00           H  
HETATM   44  H23 UNL     1      -1.037  -0.816  -2.138  1.00  0.00           H  
HETATM   45  H24 UNL     1       1.911   0.230   1.661  1.00  0.00           H  
HETATM   46  H25 UNL     1       2.974   2.293   1.134  1.00  0.00           H  
HETATM   47  H26 UNL     1       2.850   2.020  -0.648  1.00  0.00           H  
HETATM   48  H27 UNL     1       4.902   1.134   1.296  1.00  0.00           H  
HETATM   49  H28 UNL     1       4.888   0.915  -0.514  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3   17   20
CONECT    3    4   25   26
CONECT    4    5   27   28
CONECT    5    6   15   29
CONECT    6    7   17   30
CONECT    7    8   31   32
CONECT    8    9   33   34
CONECT    9   10   15   35
CONECT   10   11   36   37
CONECT   11   12   12   13
CONECT   13   14   38   39
CONECT   14   15   40   41
CONECT   15   16
CONECT   16   42   43   44
CONECT   17   18   45
CONECT   18   19   46   47
CONECT   19   20   48   49
CONECT   20   21   21
END

HMDB0000899
     RDKit          3D
Androstanedione
 49 52  0  0  0  0  0  0  0  0999 V2000
    2.7485   -0.6092   -1.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6175   -0.7646   -0.0668 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8505   -1.9608    0.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3948   -1.8210    0.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2109   -0.5271    0.5011 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6336    0.6518    0.0142 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0828    1.9601    0.4624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3825    2.1096    0.3822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1835    0.8741    0.6083 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5922    1.1470    0.1171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3946   -0.0747   -0.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6152    0.0396    0.0333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8391   -1.4166   -0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475   -1.5325    0.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5819   -0.3500   -0.0637 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5924   -0.0836   -1.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9857    0.4525    0.5870 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9781    1.5149    0.3298 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3135    0.7971    0.4224 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9804   -0.6707    0.5147 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7003   -1.5294    0.9692 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1704   -1.4367   -2.0391 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4899    0.3844   -1.9328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8153   -0.7905   -1.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2212   -2.8340   -0.2602 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0972   -2.2317    1.4021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2250   -1.9557   -1.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1283   -2.6407    0.6594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2922   -0.4706    1.6097 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6402    0.5712   -1.0931 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5496    2.7551   -0.1891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4819    2.1930    1.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6985    2.8542    1.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7367    2.5841   -0.5793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2806    0.6187    1.7015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0954    1.7988    0.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936    1.7037   -0.8542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8460   -1.7244   -1.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4520   -2.2067    0.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0254   -2.4899   -0.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5329   -1.5368    1.4128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6807   -0.0903   -1.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2618    0.9631   -1.7229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0372   -0.8160   -2.1379 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9108    0.2299    1.6610 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9737    2.2925    1.1342 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8505    2.0202   -0.6479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9021    1.1338    1.2957 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8877    0.9148   -0.5142 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  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  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
  6 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 17  2  1  0
 20  2  1  0
 15  5  1  0
 15  9  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  1
  6 30  1  6
  7 31  1  0
  7 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  1
 10 36  1  0
 10 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  0
 14 41  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  1
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
5alpha-Androstan-3,17-dione	ChEBI
5a-Androstan-3,17-dione	Generator
5Α-androstan-3,17-dione	Generator
(5a)-Androstane-3,17-dione	HMDB
5-alpha-Androstane-3,17-dione	HMDB
5a-Androsta-3,17-dione	HMDB
5a-Androstane-3, 17-dione	HMDB
5a-Androstane-3,17-dione	HMDB
5a-Androstanedione	HMDB
5alpha-Androstane-3,17-dione	HMDB
Androstane-3,17-dione	HMDB
Androstane-3,7-dione	HMDB
Androstane-3,17-dione, (2-3(H)-labeled, (2beta,5beta))-isomer	HMDB
Androstane-3,17-dione, (4-(3)H-labeled, (4alpha,5beta))-isomer	HMDB
Androstane-3,17-dione, (2-3(H)-labeled, (2alpha,5beta))-isomer	HMDB
Androstane-3,17-dione, (4-(3)H-labeled, (4beta,5beta))-isomer	HMDB
Androstane-3,17-dione, (5beta)-isomer	HMDB
3,17-Dioxy-5 alpha-androstane	HMDB
5 alpha-Androstanedione	HMDB
5 beta-Androstane-3,17-dione	HMDB
5 alpha-Androstane-3,17-dione	HMDB
Androstane-3,17-dione, (5alpha)-isomer	HMDB

Chemical Formula

C₁₉H₂₈O₂

Average Molecular Weight

288.4244

Monoisotopic Molecular Weight

288.20893014

IUPAC Name

(1S,2S,7S,10R,11S,15S)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-5,14-dione

Traditional Name

(1S,2S,7S,10R,11S,15S)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-5,14-dione

CAS Registry Number

846-46-8

SMILES

[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])CC(=O)CC[C@]12C

InChI Identifier

InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12,14-16H,3-11H2,1-2H3/t12-,14-,15-,16-,18-,19-/m0/s1

InChI Key

RAJWOBJTTGJROA-WZNAKSSCSA-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-oxo-5-alpha-steroid
Oxosteroid
17-oxosteroid
3-oxosteroid
Cyclic ketone
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

androstane-3,17-dione (CHEBI:15994 )
C19 steroids (androgens) and derivatives (LMST02020085 )

Ontology

Not Available

Blood (HMDB: HMDB0000899)
Urine (HMDB: HMDB0000899)

Tissue substructure

Hepatic tissue (HMDB: HMDB0000899)

Organ

Testis (HMDB: HMDB0000899)

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 17716701)

Cellular substructure

Membrane (HMDB: HMDB0000899)
Extracellular (HMDB: HMDB0000899)

Organelle

Endoplasmic reticulum (HMDB: HMDB0000899)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0000899)

Source

Endogenous

Endogenous (HMDB: HMDB0000899)

Exogenous

Food

Food (HMDB: HMDB0000899)

Animal origin

Poultry

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Role

Biological role

Membrane stabilizer (HMDB: HMDB0000899)

Molecular messenger

Hormone (HMDB: HMDB0000899)

Industrial application

Pharmaceutical industry

Pharmaceutical (HMDB: HMDB0000899)

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0000899)

Emulsifier (HMDB: HMDB0000899)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	133.5 - 134.0 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct Type	Data Source	CCS Value (Å²)	Reference
[M-H]-	Not Available	174.32	http://allccs.zhulab.cn/database/detail?ID=AllCCS00000226
[M+H]+	Not Available	180.954	http://allccs.zhulab.cn/database/detail?ID=AllCCS00000226

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0074 g/L	ALOGPS
logP	3.4	ALOGPS
logP	3.97	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	19.78	ChemAxon
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	34.14 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	82.78 m³·mol⁻¹	ChemAxon
Polarizability	33.83 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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
DarkChem	[M+H]+	171.312	31661259
DarkChem	[M-H]-	169.591	31661259
AllCCS	[M+H]+	173.463	32859911
AllCCS	[M-H]-	178.838	32859911
DeepCCS	[M-2H]-	205.498	30932474
DeepCCS	[M+Na]+	180.519	30932474
AllCCS	[M+H]+	173.5	32859911
AllCCS	[M+H-H2O]+	170.4	32859911
AllCCS	[M+NH4]+	176.3	32859911
AllCCS	[M+Na]+	177.1	32859911
AllCCS	[M-H]-	178.8	32859911
AllCCS	[M+Na-2H]-	178.9	32859911
AllCCS	[M+HCOO]-	179.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Androstanedione	[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])CC(=O)CC[C@]12C	2613.0	Standard polar	33892256
Androstanedione	[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])CC(=O)CC[C@]12C	2432.3	Standard non polar	33892256
Androstanedione	[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])CC(=O)CC[C@]12C	2629.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Androstanedione,1TMS,isomer #1	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(=O)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)C	2620.6	Semi standard non polar	33892256
Androstanedione,1TMS,isomer #1	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(=O)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)C	2459.1	Standard non polar	33892256
Androstanedione,1TMS,isomer #1	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(=O)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)C	2889.7	Standard polar	33892256
Androstanedione,1TMS,isomer #2	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CCC2=O	2604.5	Semi standard non polar	33892256
Androstanedione,1TMS,isomer #2	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CCC2=O	2496.8	Standard non polar	33892256
Androstanedione,1TMS,isomer #2	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CCC2=O	2991.4	Standard polar	33892256
Androstanedione,1TMS,isomer #3	C[C@]12CC[C@H]3[C@@H](CC[C@H]4C=C(O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CCC2=O	2583.4	Semi standard non polar	33892256
Androstanedione,1TMS,isomer #3	C[C@]12CC[C@H]3[C@@H](CC[C@H]4C=C(O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CCC2=O	2503.5	Standard non polar	33892256
Androstanedione,1TMS,isomer #3	C[C@]12CC[C@H]3[C@@H](CC[C@H]4C=C(O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CCC2=O	2988.7	Standard polar	33892256
Androstanedione,2TMS,isomer #1	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)C	2648.3	Semi standard non polar	33892256
Androstanedione,2TMS,isomer #1	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)C	2546.7	Standard non polar	33892256
Androstanedione,2TMS,isomer #1	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(O[Si](C)(C)C)=CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)C	2957.8	Standard polar	33892256
Androstanedione,2TMS,isomer #2	C[C@]12CC[C@H]3[C@@H](CC[C@H]4C=C(O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)C	2656.3	Semi standard non polar	33892256
Androstanedione,2TMS,isomer #2	C[C@]12CC[C@H]3[C@@H](CC[C@H]4C=C(O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)C	2569.7	Standard non polar	33892256
Androstanedione,2TMS,isomer #2	C[C@]12CC[C@H]3[C@@H](CC[C@H]4C=C(O[Si](C)(C)C)CC[C@@]43C)[C@@H]1CC=C2O[Si](C)(C)C	2956.9	Standard polar	33892256
Androstanedione,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CC[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C	2859.5	Semi standard non polar	33892256
Androstanedione,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CC[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C	2604.0	Standard non polar	33892256
Androstanedione,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC[C@H]2[C@@H]3CC[C@H]4CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C	3050.2	Standard polar	33892256
Androstanedione,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)[C@@H](CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@@H]32)C1	2839.6	Semi standard non polar	33892256
Androstanedione,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)[C@@H](CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@@H]32)C1	2711.8	Standard non polar	33892256
Androstanedione,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)[C@@H](CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@@H]32)C1	3150.9	Standard polar	33892256
Androstanedione,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=C[C@@H]2CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@@H]3[C@@]2(C)CC1	2804.1	Semi standard non polar	33892256
Androstanedione,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=C[C@@H]2CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@@H]3[C@@]2(C)CC1	2728.5	Standard non polar	33892256
Androstanedione,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1=C[C@@H]2CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@@H]3[C@@]2(C)CC1	3149.1	Standard polar	33892256
Androstanedione,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)[C@@H](CC[C@H]3[C@@H]4CC=C(O[Si](C)(C)C(C)(C)C)[C@@]4(C)CC[C@@H]32)C1	3174.0	Semi standard non polar	33892256
Androstanedione,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)[C@@H](CC[C@H]3[C@@H]4CC=C(O[Si](C)(C)C(C)(C)C)[C@@]4(C)CC[C@@H]32)C1	2806.4	Standard non polar	33892256
Androstanedione,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1=CC[C@@]2(C)[C@@H](CC[C@H]3[C@@H]4CC=C(O[Si](C)(C)C(C)(C)C)[C@@]4(C)CC[C@@H]32)C1	3199.0	Standard polar	33892256
Androstanedione,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=C[C@@H]2CC[C@H]3[C@@H]4CC=C(O[Si](C)(C)C(C)(C)C)[C@@]4(C)CC[C@@H]3[C@@]2(C)CC1	3171.0	Semi standard non polar	33892256
Androstanedione,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=C[C@@H]2CC[C@H]3[C@@H]4CC=C(O[Si](C)(C)C(C)(C)C)[C@@]4(C)CC[C@@H]3[C@@]2(C)CC1	2825.3	Standard non polar	33892256
Androstanedione,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1=C[C@@H]2CC[C@H]3[C@@H]4CC=C(O[Si](C)(C)C(C)(C)C)[C@@]4(C)CC[C@@H]3[C@@]2(C)CC1	3199.0	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental GC-MS	GC-MS Spectrum - Androstanedione GC-MS (Non-derivatized)	splash10-003u-9711000000-845e34a01c44999f2ded	2014-06-16	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Androstanedione EI-B (Non-derivatized)	splash10-000i-2790000000-3265da77fd4cc7bfa1c9	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Androstanedione GC-MS (Non-derivatized)	splash10-003u-9711000000-845e34a01c44999f2ded	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Androstanedione GC-MS (Non-derivatized) - 70eV, Positive	splash10-03ea-0490000000-e4819053bc47c4809a6c	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Androstanedione GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - Androstanedione Quattro_QQQ 10V, Positive-QTOF (Annotated)	splash10-000i-0090000000-decf354145d0bc46e624	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Androstanedione Quattro_QQQ 25V, Positive-QTOF (Annotated)	splash10-01vk-4910000000-1f05b00fe5f61dd134c3	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Androstanedione Quattro_QQQ 40V, Positive-QTOF (Annotated)	splash10-05ng-9800000000-ef0555e1d54150aaffd2	2012-07-24	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Androstanedione Linear Ion Trap , negative-QTOF	splash10-0aou-0290000000-ffd1b454b311f471cb73	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Androstanedione Linear Ion Trap , positive-QTOF	splash10-014i-0390000000-f4995b2047bec58846f5	2017-09-14	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - Androstanedione Linear Ion Trap , positive-QTOF	splash10-00di-0390000000-a4cf943964aae2cffee6	2017-09-14	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 10V, Positive-QTOF	splash10-000i-0190000000-8b26abdeab6d06d616e3	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 20V, Positive-QTOF	splash10-05a9-0490000000-5411cf1f548c371b71f5	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 40V, Positive-QTOF	splash10-0mkg-2690000000-fd3043c5fcf860949b79	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 10V, Negative-QTOF	splash10-000i-0090000000-be391ca3b57229eb2b28	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 20V, Negative-QTOF	splash10-000i-0090000000-0c9ee67f63fb1f48c00a	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 40V, Negative-QTOF	splash10-052f-3190000000-4d4ec5ab2ebbcfdebbd0	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 10V, Positive-QTOF	splash10-000i-0090000000-a3a5ee5e1cdb4d550aac	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 20V, Positive-QTOF	splash10-0h90-0970000000-66d8653b98d2df4aa327	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 40V, Positive-QTOF	splash10-0a4i-1900000000-2a46c86775b66edae018	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 10V, Negative-QTOF	splash10-000i-0090000000-383f8ad782110ec64fbf	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 20V, Negative-QTOF	splash10-000i-0090000000-383f8ad782110ec64fbf	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Androstanedione 40V, Negative-QTOF	splash10-0f79-0090000000-0497207bd4a67a50d8d8	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Experimental 1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, experimental)	2012-12-04	Wishart Lab	View Spectrum
Experimental 2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, CDCl₃, experimental)	2012-12-05	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane (predicted from logP)
Endoplasmic reticulum

Biospecimen Locations

Blood

Tissue Locations

Testis

Pathways

Name	SMPDB/PathBank	KEGG
Androstenedione Metabolism		Not Available

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	0.00036 (0.00020-0.00070) uM	Adult (>18 years old)	Male	Normal	17716701	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

DB01561

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022307

KNApSAcK ID

Not Available

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Wikipedia Link

METLIN ID

PubChem Compound

PDB ID

Not Available

ChEBI ID

15994

Food Biomarker Ontology

Not Available

VMH ID

ANDRSTANDN

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Marker, Russell E.; Kamm, Oliver; Jones, David M.; Oakwood, Thomas S. Sterols. VIII. Preparation of androstanedione from allopregnanediol. Journal of the American Chemical Society (1937), 59 614-16.

Material Safety Data Sheet (MSDS)

Download (PDF)

General References

Karlsson T, Vahlquist A, Kedishvili N, Torma H: 13-cis-retinoic acid competitively inhibits 3 alpha-hydroxysteroid oxidation by retinol dehydrogenase RoDH-4: a mechanism for its anti-androgenic effects in sebaceous glands? Biochem Biophys Res Commun. 2003 Mar 28;303(1):273-8. [PubMed:12646198 ]
Gonzalez-Santos MR, Gaja-Rodriguez OV, Alonso-Uriarte R, Sojo-Aranda I, Cortes-Gallegos V: Sleep deprivation and adaptive hormonal responses of healthy men. Arch Androl. 1989;22(3):203-7. [PubMed:2757458 ]

Enzymes

Enzyme Details

1. Aldo-keto reductase family 1 member C4

General function:: Involved in oxidoreductase activity
Specific function:: Catalyzes the transformation of the potent androgen dihydrotestosterone (DHT) into the less active form, 5-alpha-androstan-3-alpha,17-beta-diol (3-alpha-diol). Also has some 20-alpha-hydroxysteroid dehydrogenase activity. The biotransformation of the pesticide chlordecone (kepone) to its corresponding alcohol leads to increased biliary excretion of the pesticide and concomitant reduction of its neurotoxicity since bile is the major excretory route.
Gene Name:: AKR1C4
Uniprot ID:: P17516
Molecular weight:: 37094.57

Reactions

Androsterone + NAD → Androstanedione + NADH + Hydrogen Ion	details
Androsterone + NADP → Androstanedione + NADPH + Hydrogen Ion	details

Enzyme Details

2. Aldo-keto reductase family 1 member C1

General function:: Involved in oxidoreductase activity
Specific function:: Converts progesterone to its inactive form, 20-alpha-dihydroxyprogesterone (20-alpha-OHP). In the liver and intestine, may have a role in the transport of bile. May have a role in monitoring the intrahepatic bile acid concentration. Has a low bile-binding ability. May play a role in myelin formation.
Gene Name:: AKR1C1
Uniprot ID:: Q04828
Molecular weight:: 36788.02

Enzyme Details

3. Aldo-keto reductase family 1 member C2

General function:: Involved in oxidoreductase activity
Specific function:: Works in concert with the 5-alpha/5-beta-steroid reductases to convert steroid hormones into the 3-alpha/5-alpha and 3-alpha/5-beta-tetrahydrosteroids. Catalyzes the inactivation of the most potent androgen 5-alpha-dihydrotestosterone (5-alpha-DHT) to 5-alpha-androstane-3-alpha,17-beta-diol (3-alpha-diol). Has a high bile-binding ability.
Gene Name:: AKR1C2
Uniprot ID:: P52895
Molecular weight:: 15747.91

Enzyme Details

4. 3-oxo-5-beta-steroid 4-dehydrogenase

General function:: Involved in oxidoreductase activity
Specific function:: Efficiently catalyzes the reduction of progesterone, androstenedione, 17-alpha-hydroxyprogesterone and testosterone to 5-beta-reduced metabolites. The bile acid intermediates 7-alpha,12-alpha-dihydroxy-4-cholesten-3-one and 7-alpha-hydroxy-4-cholesten-3-one can also act as substrates.
Gene Name:: AKR1D1
Uniprot ID:: P51857
Molecular weight:: 32889.38

Enzyme Details

5. 3-oxo-5-alpha-steroid 4-dehydrogenase 2

General function:: Involved in 3-oxo-5-alpha-steroid 4-dehydrogenase activity
Specific function:: Converts testosterone (T) into 5-alpha-dihydrotestosterone (DHT) and progesterone or corticosterone into their corresponding 5-alpha-3-oxosteroids. It plays a central role in sexual differentiation and androgen physiology.
Gene Name:: SRD5A2
Uniprot ID:: P31213
Molecular weight:: 28407.035

Reactions

Androstanedione + Acceptor → Androstenedione + Reduced acceptor	details

Enzyme Details

6. 3-oxo-5-alpha-steroid 4-dehydrogenase 1

General function:: Involved in 3-oxo-5-alpha-steroid 4-dehydrogenase activity
Specific function:: Converts testosterone into 5-alpha-dihydrotestosterone and progesterone or corticosterone into their corresponding 5-alpha-3-oxosteroids. It plays a central role in sexual differentiation and androgen physiology.
Gene Name:: SRD5A1
Uniprot ID:: P18405
Molecular weight:: 29458.18

Reactions

Androstanedione + Acceptor → Androstenedione + Reduced acceptor	details

Enzyme Details

7. Polyprenol reductase

General function:: Involved in oxidoreductase activity, acting on the CH-CH group of donors
Specific function:: Plays a key role in early steps of protein N-linked glycosylation by being required for the conversion of polyprenol into dolichol. Dolichols are required for the synthesis of dolichol-linked monosaccharides and the oligosaccharide precursor used for N-glycosylation. Acts as a polyprenol reductase that promotes the reduction of the alpha-isoprene unit of polyprenols into dolichols in a NADP-dependent mechanism. Also able to convert testosterone (T) into 5-alpha-dihydrotestosterone (DHT).
Gene Name:: SRD5A3
Uniprot ID:: Q9H8P0
Molecular weight:: 36521.005

Reactions

Androstanedione + Acceptor → Androstenedione + Reduced acceptor	details

Showing metabocard for Androstanedione (HMDB0000899)

MOL for HMDB0000899 (Androstanedione)

3D MOL for HMDB0000899 (Androstanedione)

3D SDF for HMDB0000899 (Androstanedione)

3D-SDF for HMDB0000899 (Androstanedione)

PDB for HMDB0000899 (Androstanedione)

3D PDB for HMDB0000899 (Androstanedione)

SMILES for HMDB0000899 (Androstanedione)

INCHI for HMDB0000899 (Androstanedione)

Structure for HMDB0000899 (Androstanedione)

3D Structure for HMDB0000899 (Androstanedione)

Experimental Collision Cross Sections

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

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