MiMeDB: Showing metabocard for Epiandrosterone sulfate (MMDBc0000700)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:53:02 UTC

Update Date

2024-04-30 19:33:34 UTC

Metabolite ID

MMDBc0000700

Metabolite Identification

Common Name

Epiandrosterone sulfate

Description

Epiandrosterone sulfate, also known as (3beta,5alpha)-17-oxoandrostan-3-yl hydrogen sulfate or epiandrosterone sulphuric acid, is a member of the class of compounds known as sulfated steroids. Sulfated steroids are sterol lipids containing a sulfate group attached to the steroid skeleton. Epiandrosterone sulfate is practically insoluble (in water) and an extremely strong acidic compound (based on its pKa). Epiandrosterone sulfate can be synthesized from 5alpha-androstane and synthesized into epiandrosterone. Epiandrosterone sulfate can be found in blood and feces.

Structure

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


  Mrv1652303102017002D          

 29 32  0  0  1  0            999 V2000
   13.9473   -5.2944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2329   -3.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2329   -5.7068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5183   -5.2944    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.8038   -4.0568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9473   -2.8194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8038   -5.7068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0896   -4.4694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0896   -5.2944    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.3749   -5.7068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5183   -6.1194    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.4464   -4.3118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9313   -3.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4464   -2.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7014   -2.1922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2329   -4.0568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.2329   -4.8818    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.9473   -4.4694    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.9473   -3.6444    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5183   -4.4694    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.5183   -3.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6617   -3.2318    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6617   -2.4069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6617   -4.0568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6617   -4.8818    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6605   -5.2944    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.9459   -5.7069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0730   -4.5798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2480   -4.5798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 18 16  1  0  0  0  0
 24 18  1  0  0  0  0
 18  1  1  0  0  0  0
 16 20  1  0  0  0  0
 16  2  1  0  0  0  0
  1  3  1  0  0  0  0
 20  4  1  0  0  0  0
 20  5  1  0  0  0  0
  2  6  1  0  0  0  0
  4  7  1  0  0  0  0
  5  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 22  6  1  0  0  0  0
  4  3  1  0  0  0  0
  8  9  1  0  0  0  0
  4 11  1  6  0  0  0
 22 14  1  0  0  0  0
 24 22  1  0  0  0  0
 24 12  1  0  0  0  0
 14 13  1  0  0  0  0
 12 13  1  0  0  0  0
 14 15  2  0  0  0  0
 16 17  1  6  0  0  0
 18 19  1  1  0  0  0
 20 21  1  1  0  0  0
 22 23  1  1  0  0  0
 24 25  1  6  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 26 29  2  0  0  0  0
M  END

HMDB0062657
     RDKit          3D
Epiandrosterone sulfate
 55 58  0  0  0  0  0  0  0  0999 V2000
   -3.6767   -0.2247    1.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4664   -0.2397   -0.2217 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8454   -1.4923   -0.7245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4557   -1.6555   -0.1845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5848   -0.4472   -0.3813 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3065    0.7536    0.1469 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4608    1.9877    0.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6881    1.6243    1.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5106    0.6154    0.3809 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8798    0.4196    0.9486 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6916   -0.3266   -0.1157 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9412   -0.5326    0.4000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0933    0.2723   -0.5435 S   0  0  0  0  0  6  0  0  0  0  0  0
    5.5747    0.5115   -1.9228 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4232    1.6192    0.0754 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5443   -0.5921   -0.5676 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0102   -1.6409   -0.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5894   -1.4548   -0.8676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7691   -0.6656    0.1638 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6875   -1.5312    1.3866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5474    0.9151   -0.6542 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3780    2.0951   -0.3547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7764    1.6559   -0.7328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7156    0.1541   -0.8683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5809   -0.4732   -1.4176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5811    0.7919    1.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0421   -0.9305    1.8182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7482   -0.5183    1.4609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9089   -1.5265   -1.8128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4477   -2.3521   -0.3225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5460   -1.9522    0.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9644   -2.5065   -0.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4928   -0.3035   -1.4944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6145    0.5040    1.2038 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0021    2.1735   -0.7502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0656    2.8036    0.6203 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2638    1.1746    2.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3411    2.4888    1.3611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6398    1.0899   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3165    1.4486    1.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9146   -0.0682    1.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6911    0.3003   -1.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6835   -0.9635    0.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0642   -2.3098    0.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5624   -2.1342   -1.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1226   -2.4435   -0.9453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816   -0.9725   -1.8443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0438   -1.2178    2.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3954   -2.5605    1.0256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6633   -1.6788    1.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4031    0.7992   -1.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1063    2.9164   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3025    2.5112    0.6474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1302    2.1221   -1.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4533    1.9675    0.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  2  0
 13 16  1  0
 11 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  1
  6 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 21  2  1  0
 24  2  1  0
 19  5  1  0
 19  9  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  6
  6 34  1  1
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  6
 10 40  1  0
 10 41  1  0
 11 42  1  6
 16 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 20 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  6
 22 52  1  0
 22 53  1  0
 23 54  1  0
 23 55  1  0
M  END


  Mrv1652303102017002D          

 29 32  0  0  1  0            999 V2000
   13.9473   -5.2944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2329   -3.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2329   -5.7068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5183   -5.2944    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.8038   -4.0568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9473   -2.8194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8038   -5.7068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0896   -4.4694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0896   -5.2944    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.3749   -5.7068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5183   -6.1194    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.4464   -4.3118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9313   -3.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4464   -2.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7014   -2.1922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2329   -4.0568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.2329   -4.8818    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.9473   -4.4694    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.9473   -3.6444    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5183   -4.4694    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.5183   -3.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6617   -3.2318    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6617   -2.4069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6617   -4.0568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6617   -4.8818    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6605   -5.2944    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.9459   -5.7069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0730   -4.5798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2480   -4.5798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 18 16  1  0  0  0  0
 24 18  1  0  0  0  0
 18  1  1  0  0  0  0
 16 20  1  0  0  0  0
 16  2  1  0  0  0  0
  1  3  1  0  0  0  0
 20  4  1  0  0  0  0
 20  5  1  0  0  0  0
  2  6  1  0  0  0  0
  4  7  1  0  0  0  0
  5  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 22  6  1  0  0  0  0
  4  3  1  0  0  0  0
  8  9  1  0  0  0  0
  4 11  1  6  0  0  0
 22 14  1  0  0  0  0
 24 22  1  0  0  0  0
 24 12  1  0  0  0  0
 14 13  1  0  0  0  0
 12 13  1  0  0  0  0
 14 15  2  0  0  0  0
 16 17  1  6  0  0  0
 18 19  1  1  0  0  0
 20 21  1  1  0  0  0
 22 23  1  1  0  0  0
 24 25  1  6  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 26 29  2  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000700

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C19H30O5S/c1-18-9-7-13(24-25(21,22)23)11-12(18)3-4-14-15-5-6-17(20)19(15,2)10-8-16(14)18/h12-16H,3-11H2,1-2H3,(H,21,22,23)/t12-,13-,14-,15-,16-,18-,19-/m0/s1

> <INCHI_KEY>
ZMITXKRGXGRMKS-LUJOEAJASA-N

> <FORMULA>
C19H30O5S

> <MOLECULAR_WEIGHT>
370.5

> <EXACT_MASS>
370.18139524

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
40.49899089441635

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1S,2S,5S,7S,10R,11S,15S)-2,15-dimethyl-14-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-yl]oxidanesulfonic acid

> <ALOGPS_LOGP>
0.45

> <JCHEM_LOGP>
3.8222703046666666

> <ALOGPS_LOGS>
-4.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
19.961719950339404

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.3307185708846694

> <JCHEM_PKA_STRONGEST_BASIC>
-7.475645879362316

> <JCHEM_POLAR_SURFACE_AREA>
80.67

> <JCHEM_REFRACTIVITY>
93.80069999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.81e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,2S,5S,7S,10R,11S,15S)-2,15-dimethyl-14-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-yl]oxidanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0062657
     RDKit          3D
Epiandrosterone sulfate
 55 58  0  0  0  0  0  0  0  0999 V2000
   -3.6767   -0.2247    1.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4664   -0.2397   -0.2217 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8454   -1.4923   -0.7245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4557   -1.6555   -0.1845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5848   -0.4472   -0.3813 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3065    0.7536    0.1469 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4608    1.9877    0.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6881    1.6243    1.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5106    0.6154    0.3809 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8798    0.4196    0.9486 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6916   -0.3266   -0.1157 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9412   -0.5326    0.4000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0933    0.2723   -0.5435 S   0  0  0  0  0  6  0  0  0  0  0  0
    5.5747    0.5115   -1.9228 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4232    1.6192    0.0754 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5443   -0.5921   -0.5676 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0102   -1.6409   -0.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5894   -1.4548   -0.8676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7691   -0.6656    0.1638 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6875   -1.5312    1.3866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5474    0.9151   -0.6542 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3780    2.0951   -0.3547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7764    1.6559   -0.7328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7156    0.1541   -0.8683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5809   -0.4732   -1.4176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5811    0.7919    1.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0421   -0.9305    1.8182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7482   -0.5183    1.4609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9089   -1.5265   -1.8128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4477   -2.3521   -0.3225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5460   -1.9522    0.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9644   -2.5065   -0.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4928   -0.3035   -1.4944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6145    0.5040    1.2038 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0021    2.1735   -0.7502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0656    2.8036    0.6203 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2638    1.1746    2.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3411    2.4888    1.3611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6398    1.0899   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3165    1.4486    1.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9146   -0.0682    1.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6911    0.3003   -1.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6835   -0.9635    0.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0642   -2.3098    0.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5624   -2.1342   -1.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1226   -2.4435   -0.9453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816   -0.9725   -1.8443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0438   -1.2178    2.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3954   -2.5605    1.0256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6633   -1.6788    1.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4031    0.7992   -1.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1063    2.9164   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3025    2.5112    0.6474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1302    2.1221   -1.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4533    1.9675    0.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  2  0
 13 16  1  0
 11 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  1
  6 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 21  2  1  0
 24  2  1  0
 19  5  1  0
 19  9  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  6
  6 34  1  1
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  6
 10 40  1  0
 10 41  1  0
 11 42  1  6
 16 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 20 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  6
 22 52  1  0
 22 53  1  0
 23 54  1  0
 23 55  1  0
M  END

HEADER    PROTEIN                                 10-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-MAR-20         0                                  
HETATM    1  C   UNK     0      26.035  -9.883   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      24.701  -6.033   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      24.701 -10.653   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      23.367  -9.883   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      22.034  -7.573   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      26.035  -5.263   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      22.034 -10.653   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      20.701  -8.343   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.701  -9.883   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      19.366 -10.653   0.000  0.00  0.00           O+0
HETATM   11  H   UNK     0      23.367 -11.423   0.000  0.00  0.00           H+0
HETATM   12  C   UNK     0      28.833  -8.049   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      29.738  -6.803   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      28.833  -5.557   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      29.309  -4.092   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      24.701  -7.573   0.000  0.00  0.00           C+0
HETATM   17  H   UNK     0      24.701  -9.113   0.000  0.00  0.00           H+0
HETATM   18  C   UNK     0      26.035  -8.343   0.000  0.00  0.00           C+0
HETATM   19  H   UNK     0      26.035  -6.803   0.000  0.00  0.00           H+0
HETATM   20  C   UNK     0      23.367  -8.343   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      23.367  -6.803   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      27.369  -6.033   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      27.369  -4.493   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      27.369  -7.573   0.000  0.00  0.00           C+0
HETATM   25  H   UNK     0      27.369  -9.113   0.000  0.00  0.00           H+0
HETATM   26  S   UNK     0      18.033  -9.883   0.000  0.00  0.00           S+0
HETATM   27  O   UNK     0      16.699 -10.653   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      18.803  -8.549   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      17.263  -8.549   0.000  0.00  0.00           O+0
CONECT    1   18    3                                                       
CONECT    2   16    6                                                       
CONECT    3    1    4                                                       
CONECT    4   20    7    3   11                                             
CONECT    5   20    8                                                       
CONECT    6    2   22                                                       
CONECT    7    4    9                                                       
CONECT    8    5    9                                                       
CONECT    9    7   10    8                                                  
CONECT   10    9   26                                                       
CONECT   11    4                                                            
CONECT   12   24   13                                                       
CONECT   13   14   12                                                       
CONECT   14   22   13   15                                                  
CONECT   15   14                                                            
CONECT   16   18   20    2   17                                             
CONECT   17   16                                                            
CONECT   18   16   24    1   19                                             
CONECT   19   18                                                            
CONECT   20   16    4    5   21                                             
CONECT   21   20                                                            
CONECT   22    6   14   24   23                                             
CONECT   23   22                                                            
CONECT   24   18   22   12   25                                             
CONECT   25   24                                                            
CONECT   26   10   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

COMPND    HMDB0062657
HETATM    1  C1  UNL     1      -3.677  -0.225   1.276  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.466  -0.240  -0.222  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.845  -1.492  -0.725  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.456  -1.656  -0.184  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.585  -0.447  -0.381  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.307   0.754   0.147  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.461   1.988   0.232  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.688   1.624   1.184  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.511   0.615   0.381  1.00  0.00           C  
HETATM   10  C10 UNL     1       2.880   0.420   0.949  1.00  0.00           C  
HETATM   11  C11 UNL     1       3.692  -0.327  -0.116  1.00  0.00           C  
HETATM   12  O1  UNL     1       4.941  -0.533   0.400  1.00  0.00           O  
HETATM   13  S1  UNL     1       6.093   0.272  -0.544  1.00  0.00           S  
HETATM   14  O2  UNL     1       5.575   0.511  -1.923  1.00  0.00           O  
HETATM   15  O3  UNL     1       6.423   1.619   0.075  1.00  0.00           O  
HETATM   16  O4  UNL     1       7.544  -0.592  -0.568  1.00  0.00           O  
HETATM   17  C12 UNL     1       3.010  -1.641  -0.381  1.00  0.00           C  
HETATM   18  C13 UNL     1       1.589  -1.455  -0.868  1.00  0.00           C  
HETATM   19  C14 UNL     1       0.769  -0.666   0.164  1.00  0.00           C  
HETATM   20  C15 UNL     1       0.688  -1.531   1.387  1.00  0.00           C  
HETATM   21  C16 UNL     1      -2.547   0.915  -0.654  1.00  0.00           C  
HETATM   22  C17 UNL     1      -3.378   2.095  -0.355  1.00  0.00           C  
HETATM   23  C18 UNL     1      -4.776   1.656  -0.733  1.00  0.00           C  
HETATM   24  C19 UNL     1      -4.716   0.154  -0.868  1.00  0.00           C  
HETATM   25  O5  UNL     1      -5.581  -0.473  -1.418  1.00  0.00           O  
HETATM   26  H1  UNL     1      -3.581   0.792   1.710  1.00  0.00           H  
HETATM   27  H2  UNL     1      -3.042  -0.931   1.818  1.00  0.00           H  
HETATM   28  H3  UNL     1      -4.748  -0.518   1.461  1.00  0.00           H  
HETATM   29  H4  UNL     1      -2.909  -1.526  -1.813  1.00  0.00           H  
HETATM   30  H5  UNL     1      -3.448  -2.352  -0.323  1.00  0.00           H  
HETATM   31  H6  UNL     1      -1.546  -1.952   0.879  1.00  0.00           H  
HETATM   32  H7  UNL     1      -0.964  -2.507  -0.704  1.00  0.00           H  
HETATM   33  H8  UNL     1      -0.493  -0.304  -1.494  1.00  0.00           H  
HETATM   34  H9  UNL     1      -1.615   0.504   1.204  1.00  0.00           H  
HETATM   35  H10 UNL     1       0.002   2.173  -0.750  1.00  0.00           H  
HETATM   36  H11 UNL     1      -1.066   2.804   0.620  1.00  0.00           H  
HETATM   37  H12 UNL     1       0.264   1.175   2.097  1.00  0.00           H  
HETATM   38  H13 UNL     1       1.341   2.489   1.361  1.00  0.00           H  
HETATM   39  H14 UNL     1       1.640   1.090  -0.628  1.00  0.00           H  
HETATM   40  H15 UNL     1       3.317   1.449   1.098  1.00  0.00           H  
HETATM   41  H16 UNL     1       2.915  -0.068   1.921  1.00  0.00           H  
HETATM   42  H17 UNL     1       3.691   0.300  -1.010  1.00  0.00           H  
HETATM   43  H18 UNL     1       7.683  -0.963   0.344  1.00  0.00           H  
HETATM   44  H19 UNL     1       3.064  -2.310   0.489  1.00  0.00           H  
HETATM   45  H20 UNL     1       3.562  -2.134  -1.206  1.00  0.00           H  
HETATM   46  H21 UNL     1       1.123  -2.443  -0.945  1.00  0.00           H  
HETATM   47  H22 UNL     1       1.582  -0.973  -1.844  1.00  0.00           H  
HETATM   48  H23 UNL     1      -0.044  -1.218   2.126  1.00  0.00           H  
HETATM   49  H24 UNL     1       0.395  -2.561   1.026  1.00  0.00           H  
HETATM   50  H25 UNL     1       1.663  -1.679   1.894  1.00  0.00           H  
HETATM   51  H26 UNL     1      -2.403   0.799  -1.743  1.00  0.00           H  
HETATM   52  H27 UNL     1      -3.106   2.916  -1.066  1.00  0.00           H  
HETATM   53  H28 UNL     1      -3.302   2.511   0.647  1.00  0.00           H  
HETATM   54  H29 UNL     1      -5.130   2.122  -1.667  1.00  0.00           H  
HETATM   55  H30 UNL     1      -5.453   1.967   0.071  1.00  0.00           H  
CONECT    1    2   26   27   28
CONECT    2    3   21   24
CONECT    3    4   29   30
CONECT    4    5   31   32
CONECT    5    6   19   33
CONECT    6    7   21   34
CONECT    7    8   35   36
CONECT    8    9   37   38
CONECT    9   10   19   39
CONECT   10   11   40   41
CONECT   11   12   17   42
CONECT   12   13
CONECT   13   14   14   15   15
CONECT   13   16
CONECT   16   43
CONECT   17   18   44   45
CONECT   18   19   46   47
CONECT   19   20
CONECT   20   48   49   50
CONECT   21   22   51
CONECT   22   23   52   53
CONECT   23   24   54   55
CONECT   24   25   25
END

HMDB0062657
     RDKit          3D
Epiandrosterone sulfate
 55 58  0  0  0  0  0  0  0  0999 V2000
   -3.6767   -0.2247    1.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4664   -0.2397   -0.2217 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8454   -1.4923   -0.7245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4557   -1.6555   -0.1845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5848   -0.4472   -0.3813 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3065    0.7536    0.1469 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4608    1.9877    0.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6881    1.6243    1.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5106    0.6154    0.3809 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8798    0.4196    0.9486 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6916   -0.3266   -0.1157 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9412   -0.5326    0.4000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0933    0.2723   -0.5435 S   0  0  0  0  0  6  0  0  0  0  0  0
    5.5747    0.5115   -1.9228 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4232    1.6192    0.0754 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5443   -0.5921   -0.5676 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0102   -1.6409   -0.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5894   -1.4548   -0.8676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7691   -0.6656    0.1638 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6875   -1.5312    1.3866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5474    0.9151   -0.6542 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3780    2.0951   -0.3547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7764    1.6559   -0.7328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7156    0.1541   -0.8683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5809   -0.4732   -1.4176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5811    0.7919    1.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0421   -0.9305    1.8182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7482   -0.5183    1.4609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9089   -1.5265   -1.8128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4477   -2.3521   -0.3225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5460   -1.9522    0.8793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9644   -2.5065   -0.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4928   -0.3035   -1.4944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6145    0.5040    1.2038 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0021    2.1735   -0.7502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0656    2.8036    0.6203 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2638    1.1746    2.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3411    2.4888    1.3611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6398    1.0899   -0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3165    1.4486    1.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9146   -0.0682    1.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6911    0.3003   -1.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6835   -0.9635    0.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0642   -2.3098    0.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5624   -2.1342   -1.2062 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1226   -2.4435   -0.9453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816   -0.9725   -1.8443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0438   -1.2178    2.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3954   -2.5605    1.0256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6633   -1.6788    1.8939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4031    0.7992   -1.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1063    2.9164   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3025    2.5112    0.6474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1302    2.1221   -1.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4533    1.9675    0.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  2  0
 13 16  1  0
 11 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  1
  6 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 21  2  1  0
 24  2  1  0
 19  5  1  0
 19  9  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  6
  6 34  1  1
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  6
 10 40  1  0
 10 41  1  0
 11 42  1  6
 16 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 20 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  6
 22 52  1  0
 22 53  1  0
 23 54  1  0
 23 55  1  0
M  END

Synonyms

Value	Source
(3beta,5alpha)-17-Oxoandrostan-3-yl hydrogen sulfate	ChEBI
(3b,5a)-17-Oxoandrostan-3-yl hydrogen sulfate	Generator
(3b,5a)-17-Oxoandrostan-3-yl hydrogen sulfuric acid	Generator
(3b,5a)-17-Oxoandrostan-3-yl hydrogen sulphate	Generator
(3b,5a)-17-Oxoandrostan-3-yl hydrogen sulphuric acid	Generator
(3beta,5alpha)-17-Oxoandrostan-3-yl hydrogen sulfuric acid	Generator
(3beta,5alpha)-17-Oxoandrostan-3-yl hydrogen sulphate	Generator
(3beta,5alpha)-17-Oxoandrostan-3-yl hydrogen sulphuric acid	Generator
(3Β,5α)-17-oxoandrostan-3-yl hydrogen sulfate	Generator
(3Β,5α)-17-oxoandrostan-3-yl hydrogen sulfuric acid	Generator
(3Β,5α)-17-oxoandrostan-3-yl hydrogen sulphate	Generator
(3Β,5α)-17-oxoandrostan-3-yl hydrogen sulphuric acid	Generator
Epiandrosterone sulfuric acid	Generator
Epiandrosterone sulphate	Generator
Epiandrosterone sulphuric acid	Generator
3β,5α)-3-(Sulfooxy)androstan-17-one	HMDB
3β-Hydroxy-5α-androstan-17-one 3-sulfate	HMDB
3β-Hydroxy-5α-androstan-17-one monosulfate	HMDB
3β-Hydroxy-5α-androstan-17-one sulfate	HMDB
3β-Sulfate-5α-androstan-17-one	HMDB
3beta,5alpha)-3-(Sulfooxy)androstan-17-one	HMDB
3beta-Hydroxy-5alpha-androstan-17-one 3-sulfate	HMDB
3beta-Hydroxy-5alpha-androstan-17-one monosulfate	HMDB
3beta-Hydroxy-5alpha-androstan-17-one sulfate	HMDB
3beta-Sulfate-5alpha-androstan-17-one	HMDB
Epiandrosterone 3beta-sulfate	HMDB
Epi-Androsterone sulfate	HMDB
Epiandrosterone 3β-sulfate	HMDB
Epiandrosterone sulfate	HMDB
Isoandrosterone sulfate	HMDB

Molecular Formula

C₁₉H₃₀O₅S

Average Mass

370.5

Monoisotopic Mass

370.18139524

IUPAC Name

[(1S,2S,5S,7S,10R,11S,15S)-2,15-dimethyl-14-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-yl]oxidanesulfonic acid

Traditional Name

[(1S,2S,5S,7S,10R,11S,15S)-2,15-dimethyl-14-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-yl]oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C19H30O5S/c1-18-9-7-13(24-25(21,22)23)11-12(18)3-4-14-15-5-6-17(20)19(15,2)10-8-16(14)18/h12-16H,3-11H2,1-2H3,(H,21,22,23)/t12-,13-,14-,15-,16-,18-,19-/m0/s1

InChI Key

ZMITXKRGXGRMKS-LUJOEAJASA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sulfated steroids. These are sterol lipids containing a sulfate group attached to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Sulfated steroids

Direct Parent

Sulfated steroids

Alternative Parents

Substituents

Sulfated steroid skeleton
Androstane-skeleton
17-oxosteroid
Oxosteroid
Sulfuric acid ester
Sulfuric acid monoester
Sulfate-ester
Alkyl sulfate
Organic sulfuric acid or derivatives
Ketone
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

steroid sulfate (CHEBI:83040 )
17-oxo steroid (CHEBI:83040 )
androstanoid (CHEBI:83040 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0048 g/L	ALOGPS
logP	0.45	ALOGPS
logP	3.82	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	-1.3	ChemAxon
pKa (Strongest Basic)	-7.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	80.67 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	93.8 m³·mol⁻¹	ChemAxon
Polarizability	40.5 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

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Feces

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria/Eubacteria	Firmicutes	1	Human ; Human feces	Indirect association between microbiota composition and metabolites measured in host biospecimen

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified				HMDB
Human Blood	Detected but not Quantified	Adult (>18 years old)	Female	Normal	HMDB	27355821
Human Feces	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	27543620
Human Feces	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	25037050
Human Feces	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	29808030

External Links

HMDB ID

HMDB0062657

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB034849

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

9929317

PDB ID

Not Available

ChEBI ID

83040

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. doi: 10.1038/35036052. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. doi: 10.1194/jlr.R600022-JLR200. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. doi: 10.1194/jlr.R700005-JLR200. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Epiandrosterone sulfate (MMDBc0000700)

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