MiMeDB: Showing metabocard for Dehydroepiandrosterone sulfate (MMDBc0000561)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:40:34 UTC

Update Date

2022-08-31 06:08:29 UTC

Metabolite ID

MMDBc0000561

Metabolite Identification

Common Name

Dehydroepiandrosterone sulfate

Description

Dehydroepiandrosterone sulfate or DHEA-S is the sulfated form of dehydroepiandrosterone (DHEA). This sulfation is reversibly catalyzed by sulfotransferase 2A1 (SULT2A1) primarily in the adrenals, the liver, and small intestine. In the blood, most DHEA is found as DHEA-S with levels that are about 300 times higher than those of free DHEA. Orally-ingested DHEA is converted into its sulfate when passing through the intestines and liver. Whereas DHEA levels naturally reach their peak in the early morning hours, DHEAS levels show no diurnal variation. From a practical point of view, measurement of DHEA-S is preferable to DHEA since levels are more stable. DHEA (from which DHEA-S comes from) is a natural steroid prohormone produced from cholesterol by the adrenal glands, the gonads, adipose tissue, brain, and in the skin (by an autocrine mechanism). DHEA is the precursor of androstenedione, which can undergo further conversion to produce the androgen testosterone and the estrogens estrone and estradiol. DHEA is also a potent sigma-1 agonist. Serum dehydroepiandrosterone sulfate is a classic marker for adrenarche, and subsequently for the individual hormonal milieu (PMID: 10599744 ). Dehydroepiandrosterone sulfate is an endogenously produced sex steroid that has been hypothesized to have anti-aging effects (PMID: 16960027 ). It also has been inversely associated with the development of atherosclerosis (PMID: 8956025 ).

Structure

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


  Mrv1652306191804272D          

 28 31  0  0  0  0            999 V2000
10000.004110000.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.144510001.4432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.1445 9998.9596    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.8632 9998.1238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.1483 9998.5377    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7344 9999.2527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5600 9999.2527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.4291 9998.1218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.430310000.1945    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
10000.7162 9998.9596    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9999.2912 9999.7786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5767 9999.3661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5767 9998.5410    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.2912 9998.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.430810001.0246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.716310000.6121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.7163 9999.7870    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10001.4308 9999.3746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10002.1453 9999.7870    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10002.145310000.6121    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.0029 9999.3661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.0029 9998.5410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.7174 9998.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.4319 9998.5410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.9299 9999.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.414810000.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.930010000.8669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.185010001.6515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  2  0  0  0  0
  5  8  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 15 20  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 13  4  1  1  0  0  0
 11 21  1  0  0  0  0
 14 22  1  0  0  0  0
 21  1  1  1  0  0  0
 20  2  1  1  0  0  0
 19  3  1  6  0  0  0
 17 21  1  0  0  0  0
 24 18  1  0  0  0  0
 18  9  1  1  0  0  0
 17 10  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 27  1  0  0  0  0
 19 25  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

HMDB0001032
     RDKit          3D
Dehydroepiandrosterone sulfate
 53 56  0  0  0  0  0  0  0  0999 V2000
   -3.5475   -0.4532   -1.7712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3419    0.5452   -0.6798 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5573    1.7536   -1.1250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0913    1.4550   -1.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5110    0.6524   -0.1252 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3561   -0.5598    0.2015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7083   -1.3071    1.3140 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6389   -1.7385    0.8808 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3720   -0.9883    0.0921 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7180   -1.4544   -0.3169 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6883   -0.4351    0.2590 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6290    0.0046   -0.6572 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1489   -0.4515   -0.1262 S   0  0  0  0  0  6  0  0  0  0  0  0
    6.0877   -1.6994    0.7291 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0591   -0.7949   -1.2914 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8670    0.7986    0.7673 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9977    0.7122    0.9477 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8863    1.3450    0.1855 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177    0.3267   -0.4126 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2052    0.3632   -1.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7072   -0.0302    0.5520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7110   -0.9905    1.0328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0269   -0.2602    0.7745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6835    0.8942   -0.1370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3948    1.8394   -0.3213 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1700   -1.2757   -1.3643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1478    0.0429   -2.5699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6253   -0.8153   -2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7580    2.6114   -0.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9360    2.0389   -2.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8705    0.9252   -2.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5496    2.4160   -1.3020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5400    1.3035    0.7855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3533   -1.2015   -0.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2573   -2.2237    1.6153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5536   -0.6651    2.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0688   -2.6982    1.2041 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8407   -1.6249   -1.3944 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9029   -2.4681    0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2534   -0.9659    1.0792 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2035    1.0614    1.4631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6952    0.4346    2.0002 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7833    1.4998    1.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2754    1.9325    0.9148 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2600    2.0586   -0.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2925    0.1829   -2.0295 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0625    1.4107   -2.3071 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6501   -0.3963   -2.4785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5878    0.7869    1.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6060   -1.1153    2.1349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7000   -1.9760    0.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4671    0.1201    1.7253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7445   -0.9264    0.2952 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  2  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  6
  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  1
  6 34  1  6
  7 35  1  0
  7 36  1  0
  8 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  1
 16 41  1  0
 17 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 20 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  1
 22 50  1  0
 22 51  1  0
 23 52  1  0
 23 53  1  0
M  END


  Mrv1652306191804272D          

 28 31  0  0  0  0            999 V2000
10000.004110000.1945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.144510001.4432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.1445 9998.9596    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.8632 9998.1238    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.1483 9998.5377    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
 9996.7344 9999.2527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5600 9999.2527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.4291 9998.1218    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.430310000.1945    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
10000.7162 9998.9596    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9999.2912 9999.7786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5767 9999.3661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5767 9998.5410    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.2912 9998.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.430810001.0246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.716310000.6121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.7163 9999.7870    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10001.4308 9999.3746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10002.1453 9999.7870    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10002.145310000.6121    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.0029 9999.3661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.0029 9998.5410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.7174 9998.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.4319 9998.5410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.9299 9999.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.414810000.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.930010000.8669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.185010001.6515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  2  0  0  0  0
  5  8  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 16  1  0  0  0  0
 15 20  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 13  4  1  1  0  0  0
 11 21  1  0  0  0  0
 14 22  1  0  0  0  0
 21  1  1  1  0  0  0
 20  2  1  1  0  0  0
 19  3  1  6  0  0  0
 17 21  1  0  0  0  0
 24 18  1  0  0  0  0
 18  9  1  1  0  0  0
 17 10  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 27  1  0  0  0  0
 19 25  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000561

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@H](CC[C@]12C)OS(O)(=O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H28O5S/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/h3,13-16H,4-11H2,1-2H3,(H,21,22,23)/t13-,14-,15-,16-,18-,19-/m0/s1

> <INCHI_KEY>
CZWCKYRVOZZJNM-USOAJAOKSA-N

> <FORMULA>
C19H28O5S

> <MOLECULAR_WEIGHT>
368.488

> <EXACT_MASS>
368.165744696

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
39.8474725985752

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
0.49

> <JCHEM_LOGP>
3.416690823333334

> <ALOGPS_LOGS>
-4.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
19.957705855662745

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.3632754765266997

> <JCHEM_PKA_STRONGEST_BASIC>
-7.4756492107864165

> <JCHEM_POLAR_SURFACE_AREA>
80.67

> <JCHEM_REFRACTIVITY>
94.6507

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.06e-03 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0001032
     RDKit          3D
Dehydroepiandrosterone sulfate
 53 56  0  0  0  0  0  0  0  0999 V2000
   -3.5475   -0.4532   -1.7712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3419    0.5452   -0.6798 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5573    1.7536   -1.1250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0913    1.4550   -1.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5110    0.6524   -0.1252 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3561   -0.5598    0.2015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7083   -1.3071    1.3140 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6389   -1.7385    0.8808 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3720   -0.9883    0.0921 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7180   -1.4544   -0.3169 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6883   -0.4351    0.2590 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6290    0.0046   -0.6572 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1489   -0.4515   -0.1262 S   0  0  0  0  0  6  0  0  0  0  0  0
    6.0877   -1.6994    0.7291 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0591   -0.7949   -1.2914 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8670    0.7986    0.7673 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9977    0.7122    0.9477 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8863    1.3450    0.1855 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177    0.3267   -0.4126 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2052    0.3632   -1.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7072   -0.0302    0.5520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7110   -0.9905    1.0328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0269   -0.2602    0.7745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6835    0.8942   -0.1370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3948    1.8394   -0.3213 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1700   -1.2757   -1.3643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1478    0.0429   -2.5699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6253   -0.8153   -2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7580    2.6114   -0.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9360    2.0389   -2.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8705    0.9252   -2.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5496    2.4160   -1.3020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5400    1.3035    0.7855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3533   -1.2015   -0.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2573   -2.2237    1.6153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5536   -0.6651    2.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0688   -2.6982    1.2041 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8407   -1.6249   -1.3944 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9029   -2.4681    0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2534   -0.9659    1.0792 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2035    1.0614    1.4631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6952    0.4346    2.0002 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7833    1.4998    1.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2754    1.9325    0.9148 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2600    2.0586   -0.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2925    0.1829   -2.0295 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0625    1.4107   -2.3071 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6501   -0.3963   -2.4785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5878    0.7869    1.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6060   -1.1153    2.1349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7000   -1.9760    0.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4671    0.1201    1.7253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7445   -0.9264    0.2952 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  2  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  6
  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  1
  6 34  1  6
  7 35  1  0
  7 36  1  0
  8 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  1
 16 41  1  0
 17 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 20 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  1
 22 50  1  0
 22 51  1  0
 23 52  1  0
 23 53  1  0
M  END

HEADER    PROTEIN                                 19-JUN-18   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-18         0                                  
HETATM    1  C   UNK     0    8666.6748667.030   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8670.6708669.361   0.000  0.00  0.00           C+0
HETATM    3  H   UNK     0    8670.6708664.725   0.000  0.00  0.00           H+0
HETATM    4  O   UNK     0    8662.6788663.164   0.000  0.00  0.00           O+0
HETATM    5  S   UNK     0    8661.3438663.937   0.000  0.00  0.00           S+0
HETATM    6  O   UNK     0    8660.5718665.272   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0    8662.1128665.272   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0    8660.0018663.161   0.000  0.00  0.00           O+0
HETATM    9  H   UNK     0    8669.3378667.030   0.000  0.00  0.00           H+0
HETATM   10  H   UNK     0    8668.0048664.725   0.000  0.00  0.00           H+0
HETATM   11  C   UNK     0    8665.3448666.253   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8664.0108665.483   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8664.0108663.943   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8665.3448663.173   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8669.3378668.579   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8668.0048667.809   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8668.0048666.269   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8669.3378665.499   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8670.6718666.269   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8670.6718667.809   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8666.6728665.483   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8666.6728663.943   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0    8668.0068663.173   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0    8669.3408663.943   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0    8672.1368665.793   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0    8673.0418667.039   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0    8672.1368668.285   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0    8672.6128669.749   0.000  0.00  0.00           O+0
CONECT    1   21                                                            
CONECT    2   20                                                            
CONECT    3   19                                                            
CONECT    4    5   13                                                       
CONECT    5    4    6    7    8                                             
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    5                                                            
CONECT    9   18                                                            
CONECT   10   17                                                            
CONECT   11   12   21                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14    4                                                  
CONECT   14   13   22                                                       
CONECT   15   16   20                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   21   10                                             
CONECT   18   17   19   24    9                                             
CONECT   19   18   20    3   25                                             
CONECT   20   15   19    2   27                                             
CONECT   21   22   11    1   17                                             
CONECT   22   21   23   14                                                  
CONECT   23   22   24                                                       
CONECT   24   23   18                                                       
CONECT   25   26   19                                                       
CONECT   26   25   27                                                       
CONECT   27   26   20   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

COMPND    HMDB0001032
HETATM    1  C1  UNL     1      -3.548  -0.453  -1.771  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.342   0.545  -0.680  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.557   1.754  -1.125  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.091   1.455  -1.264  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.511   0.652  -0.125  1.00  0.00           C  
HETATM    6  C6  UNL     1      -1.356  -0.560   0.202  1.00  0.00           C  
HETATM    7  C7  UNL     1      -0.708  -1.307   1.314  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.639  -1.738   0.881  1.00  0.00           C  
HETATM    9  C9  UNL     1       1.372  -0.988   0.092  1.00  0.00           C  
HETATM   10  C10 UNL     1       2.718  -1.454  -0.317  1.00  0.00           C  
HETATM   11  C11 UNL     1       3.688  -0.435   0.259  1.00  0.00           C  
HETATM   12  O1  UNL     1       4.629   0.005  -0.657  1.00  0.00           O  
HETATM   13  S1  UNL     1       6.149  -0.452  -0.126  1.00  0.00           S  
HETATM   14  O2  UNL     1       6.088  -1.699   0.729  1.00  0.00           O  
HETATM   15  O3  UNL     1       7.059  -0.795  -1.291  1.00  0.00           O  
HETATM   16  O4  UNL     1       6.867   0.799   0.767  1.00  0.00           O  
HETATM   17  C12 UNL     1       2.998   0.712   0.948  1.00  0.00           C  
HETATM   18  C13 UNL     1       1.886   1.345   0.186  1.00  0.00           C  
HETATM   19  C14 UNL     1       0.918   0.327  -0.413  1.00  0.00           C  
HETATM   20  C15 UNL     1       1.205   0.363  -1.919  1.00  0.00           C  
HETATM   21  C16 UNL     1      -2.707  -0.030   0.552  1.00  0.00           C  
HETATM   22  C17 UNL     1      -3.711  -0.990   1.033  1.00  0.00           C  
HETATM   23  C18 UNL     1      -5.027  -0.260   0.774  1.00  0.00           C  
HETATM   24  C19 UNL     1      -4.684   0.894  -0.137  1.00  0.00           C  
HETATM   25  O5  UNL     1      -5.395   1.839  -0.321  1.00  0.00           O  
HETATM   26  H1  UNL     1      -4.170  -1.276  -1.364  1.00  0.00           H  
HETATM   27  H2  UNL     1      -4.148   0.043  -2.570  1.00  0.00           H  
HETATM   28  H3  UNL     1      -2.625  -0.815  -2.246  1.00  0.00           H  
HETATM   29  H4  UNL     1      -2.758   2.611  -0.455  1.00  0.00           H  
HETATM   30  H5  UNL     1      -2.936   2.039  -2.128  1.00  0.00           H  
HETATM   31  H6  UNL     1      -0.871   0.925  -2.224  1.00  0.00           H  
HETATM   32  H7  UNL     1      -0.550   2.416  -1.302  1.00  0.00           H  
HETATM   33  H8  UNL     1      -0.540   1.303   0.785  1.00  0.00           H  
HETATM   34  H9  UNL     1      -1.353  -1.202  -0.696  1.00  0.00           H  
HETATM   35  H10 UNL     1      -1.257  -2.224   1.615  1.00  0.00           H  
HETATM   36  H11 UNL     1      -0.554  -0.665   2.226  1.00  0.00           H  
HETATM   37  H12 UNL     1       1.069  -2.698   1.204  1.00  0.00           H  
HETATM   38  H13 UNL     1       2.841  -1.625  -1.394  1.00  0.00           H  
HETATM   39  H14 UNL     1       2.903  -2.468   0.148  1.00  0.00           H  
HETATM   40  H15 UNL     1       4.253  -0.966   1.079  1.00  0.00           H  
HETATM   41  H16 UNL     1       6.203   1.061   1.463  1.00  0.00           H  
HETATM   42  H17 UNL     1       2.695   0.435   2.000  1.00  0.00           H  
HETATM   43  H18 UNL     1       3.783   1.500   1.095  1.00  0.00           H  
HETATM   44  H19 UNL     1       1.275   1.933   0.915  1.00  0.00           H  
HETATM   45  H20 UNL     1       2.260   2.059  -0.553  1.00  0.00           H  
HETATM   46  H21 UNL     1       2.292   0.183  -2.029  1.00  0.00           H  
HETATM   47  H22 UNL     1       1.062   1.411  -2.307  1.00  0.00           H  
HETATM   48  H23 UNL     1       0.650  -0.396  -2.478  1.00  0.00           H  
HETATM   49  H24 UNL     1      -2.588   0.787   1.283  1.00  0.00           H  
HETATM   50  H25 UNL     1      -3.606  -1.115   2.135  1.00  0.00           H  
HETATM   51  H26 UNL     1      -3.700  -1.976   0.525  1.00  0.00           H  
HETATM   52  H27 UNL     1      -5.467   0.120   1.725  1.00  0.00           H  
HETATM   53  H28 UNL     1      -5.745  -0.926   0.295  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    9   37
CONECT    9   10   19
CONECT   10   11   38   39
CONECT   11   12   17   40
CONECT   12   13
CONECT   13   14   14   15   15
CONECT   13   16
CONECT   16   41
CONECT   17   18   42   43
CONECT   18   19   44   45
CONECT   19   20
CONECT   20   46   47   48
CONECT   21   22   49
CONECT   22   23   50   51
CONECT   23   24   52   53
CONECT   24   25   25
END

HMDB0001032
     RDKit          3D
Dehydroepiandrosterone sulfate
 53 56  0  0  0  0  0  0  0  0999 V2000
   -3.5475   -0.4532   -1.7712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3419    0.5452   -0.6798 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5573    1.7536   -1.1250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0913    1.4550   -1.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5110    0.6524   -0.1252 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3561   -0.5598    0.2015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7083   -1.3071    1.3140 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6389   -1.7385    0.8808 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3720   -0.9883    0.0921 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7180   -1.4544   -0.3169 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6883   -0.4351    0.2590 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6290    0.0046   -0.6572 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1489   -0.4515   -0.1262 S   0  0  0  0  0  6  0  0  0  0  0  0
    6.0877   -1.6994    0.7291 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0591   -0.7949   -1.2914 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8670    0.7986    0.7673 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9977    0.7122    0.9477 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8863    1.3450    0.1855 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177    0.3267   -0.4126 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2052    0.3632   -1.9190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7072   -0.0302    0.5520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7110   -0.9905    1.0328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0269   -0.2602    0.7745 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6835    0.8942   -0.1370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3948    1.8394   -0.3213 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1700   -1.2757   -1.3643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1478    0.0429   -2.5699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6253   -0.8153   -2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7580    2.6114   -0.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9360    2.0389   -2.1276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8705    0.9252   -2.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5496    2.4160   -1.3020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5400    1.3035    0.7855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3533   -1.2015   -0.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2573   -2.2237    1.6153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5536   -0.6651    2.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0688   -2.6982    1.2041 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8407   -1.6249   -1.3944 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9029   -2.4681    0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2534   -0.9659    1.0792 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2035    1.0614    1.4631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6952    0.4346    2.0002 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7833    1.4998    1.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2754    1.9325    0.9148 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2600    2.0586   -0.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2925    0.1829   -2.0295 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0625    1.4107   -2.3071 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6501   -0.3963   -2.4785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5878    0.7869    1.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6060   -1.1153    2.1349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7000   -1.9760    0.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4671    0.1201    1.7253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7445   -0.9264    0.2952 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  2  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  6
  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  1
  6 34  1  6
  7 35  1  0
  7 36  1  0
  8 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  1
 16 41  1  0
 17 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 20 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  1
 22 50  1  0
 22 51  1  0
 23 52  1  0
 23 53  1  0
M  END

Synonyms

Value	Source
(3-beta)-3-(Sulfooxy)androst-5-en-17-one	ChEBI
17-Ketoandrost-5-en-3beta-yl sulfate	ChEBI
17-Oxoandrost-5-en-3beta-yl hydrogen sulphate	ChEBI
3-O-Sulfodehydroepiandrosterone	ChEBI
3beta-Hydroxyandrost-5-en-17-one 3-sulfate	ChEBI
Androst-5-en-17-on-3beta-yl sulfuric acid	ChEBI
Dehydroepiandrosterone 3-sulfate	ChEBI
Dehydroepiandrosterone monosulfate	ChEBI
Dehydroepiandrosterone sulphate	ChEBI
Dehydroisoandrosterone sulfate	ChEBI
Dehydroisoandrosterone-3-sulfate	ChEBI
DHEA sulfate	ChEBI
DHEA-S	ChEBI
DHEAS	ChEBI
Prasterone sulfate	ChEBI
(3-b)-3-(Sulfooxy)androst-5-en-17-one	Generator
(3-b)-3-(Sulphooxy)androst-5-en-17-one	Generator
(3-beta)-3-(Sulphooxy)androst-5-en-17-one	Generator
(3-Β)-3-(sulfooxy)androst-5-en-17-one	Generator
(3-Β)-3-(sulphooxy)androst-5-en-17-one	Generator
17-Ketoandrost-5-en-3b-yl sulfate	Generator
17-Ketoandrost-5-en-3b-yl sulfuric acid	Generator
17-Ketoandrost-5-en-3b-yl sulphate	Generator
17-Ketoandrost-5-en-3b-yl sulphuric acid	Generator
17-Ketoandrost-5-en-3beta-yl sulfuric acid	Generator
17-Ketoandrost-5-en-3beta-yl sulphate	Generator
17-Ketoandrost-5-en-3beta-yl sulphuric acid	Generator
17-Ketoandrost-5-en-3β-yl sulfate	Generator
17-Ketoandrost-5-en-3β-yl sulfuric acid	Generator
17-Ketoandrost-5-en-3β-yl sulphate	Generator
17-Ketoandrost-5-en-3β-yl sulphuric acid	Generator
17-Oxoandrost-5-en-3b-yl hydrogen sulfate	Generator
17-Oxoandrost-5-en-3b-yl hydrogen sulfuric acid	Generator
17-Oxoandrost-5-en-3b-yl hydrogen sulphate	Generator
17-Oxoandrost-5-en-3b-yl hydrogen sulphuric acid	Generator
17-Oxoandrost-5-en-3beta-yl hydrogen sulfate	Generator
17-Oxoandrost-5-en-3beta-yl hydrogen sulfuric acid	Generator
17-Oxoandrost-5-en-3beta-yl hydrogen sulphuric acid	Generator
17-Oxoandrost-5-en-3β-yl hydrogen sulfate	Generator
17-Oxoandrost-5-en-3β-yl hydrogen sulfuric acid	Generator
17-Oxoandrost-5-en-3β-yl hydrogen sulphate	Generator
17-Oxoandrost-5-en-3β-yl hydrogen sulphuric acid	Generator
3-O-Sulphodehydroepiandrosterone	Generator
3b-Hydroxyandrost-5-en-17-one 3-sulfate	Generator
3b-Hydroxyandrost-5-en-17-one 3-sulfuric acid	Generator
3b-Hydroxyandrost-5-en-17-one 3-sulphate	Generator
3b-Hydroxyandrost-5-en-17-one 3-sulphuric acid	Generator
3beta-Hydroxyandrost-5-en-17-one 3-sulfuric acid	Generator
3beta-Hydroxyandrost-5-en-17-one 3-sulphate	Generator
3beta-Hydroxyandrost-5-en-17-one 3-sulphuric acid	Generator
3Β-hydroxyandrost-5-en-17-one 3-sulfate	Generator
3Β-hydroxyandrost-5-en-17-one 3-sulfuric acid	Generator
3Β-hydroxyandrost-5-en-17-one 3-sulphate	Generator
3Β-hydroxyandrost-5-en-17-one 3-sulphuric acid	Generator
Androst-5-en-17-on-3b-yl sulfate	Generator
Androst-5-en-17-on-3b-yl sulfuric acid	Generator
Androst-5-en-17-on-3b-yl sulphate	Generator
Androst-5-en-17-on-3b-yl sulphuric acid	Generator
Androst-5-en-17-on-3beta-yl sulfate	Generator
Androst-5-en-17-on-3beta-yl sulphate	Generator
Androst-5-en-17-on-3beta-yl sulphuric acid	Generator
Androst-5-en-17-on-3β-yl sulfate	Generator
Androst-5-en-17-on-3β-yl sulfuric acid	Generator
Androst-5-en-17-on-3β-yl sulphate	Generator
Androst-5-en-17-on-3β-yl sulphuric acid	Generator
Dehydroepiandrosterone 3-sulfuric acid	Generator
Dehydroepiandrosterone 3-sulphate	Generator
Dehydroepiandrosterone 3-sulphuric acid	Generator
Dehydroepiandrosterone monosulfuric acid	Generator
Dehydroepiandrosterone monosulphate	Generator
Dehydroepiandrosterone monosulphuric acid	Generator
Dehydroepiandrosterone sulfuric acid	Generator
Dehydroepiandrosterone sulphuric acid	Generator
Dehydroisoandrosterone sulfuric acid	Generator
Dehydroisoandrosterone sulphate	Generator
Dehydroisoandrosterone sulphuric acid	Generator
Dehydroisoandrosterone-3-sulfuric acid	Generator
Dehydroisoandrosterone-3-sulphate	Generator
Dehydroisoandrosterone-3-sulphuric acid	Generator
DHEA sulfuric acid	Generator
DHEA sulphate	Generator
DHEA sulphuric acid	Generator
Prasterone sulfuric acid	Generator
Prasterone sulphate	Generator
Prasterone sulphuric acid	Generator
(3beta)-3-(Sulfooxy)-androst-5-en-17-one	HMDB
17-Oxoandrost-5-en-3-yl hydrogen sulfate	HMDB
17-Oxoandrost-5-en-3-yl hydrogen sulphate	HMDB
3-b-Hydroxyandrost-5-en-17-one 3-sulfate	HMDB
3-b-Hydroxyandrost-5-en-17-one 3-sulphate	HMDB
3-beta-Hydroxyandrost-5-en-17-one 3-sulfate	HMDB
3-beta-Hydroxyandrost-5-en-17-one 3-sulphate	HMDB
3b-Hydroxy-androst-5-en-17-one hydrogen sulfate	HMDB
3b-Hydroxy-androst-5-en-17-one hydrogen sulphate	HMDB
3beta-Hydroxy-androst-5-en-17-one hydrogen sulfate	HMDB
3beta-Hydroxy-androst-5-en-17-one hydrogen sulphate	HMDB
Dehydroepiandrosterone-3-sulfate	HMDB
Dehydroepiandrosterone-3-sulphate	HMDB
Formylisoglutamic acid	HMDB
Prasterone-3-sulfate	HMDB
Prasterone-3-sulphate	HMDB
DHA sulfate	HMDB
Sulfate, dehydroisoandrosterone	HMDB
Sulfate, prasterone	HMDB
Sulfate, dhea	HMDB
Sulfate, dehydroepiandrosterone	HMDB
Sulfate, dha	HMDB

Molecular Formula

C₁₉H₂₈O₅S

Average Mass

368.488

Monoisotopic Mass

368.165744696

IUPAC Name

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

Traditional Name

[(1S,2R,5S,10R,11S,15S)-2,15-dimethyl-14-oxotetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-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=C2C[C@H](CC[C@]12C)OS(O)(=O)=O

InChI Identifier

InChI=1S/C19H28O5S/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/h3,13-16H,4-11H2,1-2H3,(H,21,22,23)/t13-,14-,15-,16-,18-,19-/m0/s1

InChI Key

CZWCKYRVOZZJNM-USOAJAOKSA-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
Delta-5-steroid
Sulfuric acid ester
Alkyl sulfate
Sulfuric acid monoester
Sulfate-ester
Organic sulfuric acid or derivatives
Ketone
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Carbonyl group
Organic oxide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

steroid sulfate (CHEBI:16814 )
17-oxo steroid (CHEBI:16814 )
sulfates (C04555 )
C19 steroids (androgens) and derivatives (C04555 )
Androgens (C04555 )
Sulfates (LMST05020010 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0081 g/L	ALOGPS
logP	0.49	ALOGPS
logP	3.42	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	-1.4	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	94.65 m³·mol⁻¹	ChemAxon
Polarizability	39.85 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

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-002f-0097000000-e6d4f60e9803940d2f55	2017-09-01	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 10V, Negative	splash10-014i-0009000000-d49a8b7164a230745f20	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 20V, Negative	splash10-014i-3009000000-bd7e895ed74eba8a0f23	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 40V, Negative	splash10-0002-9000000000-8d7ea5bd8a8a0d5219c7	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 30V, Negative	splash10-0002-9001000000-5d89a4081c0f6b0c3324	2021-09-20	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-014i-0049000000-f9a938b029283c157bdf	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00di-0091000000-c2b83d86ae8174524e1d	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0udi-5792000000-20638b1484fe342eb3c9	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-014i-0029000000-79344bc1ba3ea2c26db7	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-00kr-1092000000-3b129a6c30b2629e1661	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-008i-6090000000-35cc2726715438281170	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-014i-0009000000-c58c9c29bacda1fca240	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-014i-1009000000-d5f9b663138c7975150b	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0002-9105000000-a5c4a9d21c991c730dab	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-014i-0019000000-e7315ac14210f0dc3930	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0uk9-0292000000-06a461930592bd575f19	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0a4m-4920000000-e6055497e2f92515f76a	2021-09-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Extracellular
Membrane

Biospecimen Locations

Blood
Feces
Kidney
Liver
Placenta
Prostate
Urine

Tissue Locations

Kidney
Liver
Placenta
Prostate

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species
MMDBp0192023	Sulfotransferase family cytosolic 2B member 1	Enzyme	O00204	Homo sapiens
MMDBp0192150	Steryl-sulfatase	Unknown	P08842	Homo sapiens

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference
MMDBr0000674	Dehydroepiandrosterone sulfate	Dehydroepiandrosterone sulfate	Solute carrier organic anion transporter family, member 1a2	Dehydroepiandrosterone Sulfate Transport via Bicarbonate Antiport	VMH	12507753 9007731 9334206
MMDBr0000675	Dehydroepiandrosterone sulfate	Dehydroepiandrosterone sulfate	Not Available	Dheas Intracellular Transport	VMH	30371894
MMDBr0000676	Dehydroepiandrosterone	Dehydroepiandrosterone sulfate	Sulfotransferase family, cytosolic, 1a, phenol-preferring, member 3	Dehydroepiandrosterone Sulfotransferase	VMH	11535246 1588921
MMDBr0002177	Dehydroepiandrosterone sulfate	Dehydroepiandrosterone	Not Available	Steryl-Sulfatase	VMH	30371894
MMDBr0002178	Dehydroepiandrosterone sulfate	Dehydroepiandrosterone	Steroid sulfatase (microsomal), isozyme s	Steryl-Sulfatase	VMH	30371894
MMDBr0003618	Dehydroepiandrosterone sulfate	Dehydroepiandrosterone sulfate	Solute carrier organic anion transporter family, member 1b1	Resistance-Nodulation-Cell Division (Rnd) Tcdb:2.A.60.1.5	VMH	11076396 14579113
MMDBr0003619	Dehydroepiandrosterone sulfate	Dehydroepiandrosterone sulfate	Solute carrier organic anion transporter family, member 1b1	Resistance-Nodulation-Cell Division (Rnd) Tcdb:2.A.60.1.5	VMH	11076396 14579113
MMDBr0003703	Dehydroepiandrosterone sulfate	Dehydroepiandrosterone sulfate	Solute carrier family 22, member 10	Organic Anion Transporter 5 Utilized Transport	VMH	11023036 12739169 12856180 12883891 1554704 18021224 4553030 793184 8725559 8781017
MMDBr0005642	Adenosine triphosphate	ADP	Atp-binding cassette, sub-family c (cftr/mrp), member 11	Dhea Transport by ABCa11	VMH	30371894
MMDBr0010728	Oxoglutaric acid	Oxoglutaric acid	Solute carrier family 22 (organic anion/urate transporter), member 11	HMR_9623	VMH	30371894

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference
11-beta-hydroxylase deficiency		Association	Human Blood	HMDB	8933406
Alzheimer's disease	Slight Increase	Association	Human Blood	HMDB	8478958
Hirsutism	Increased	Association	Human Blood	HMDB	8187312
Polycystic ovary syndrome		Association	Human Blood	HMDB	15531511
Rheumatoid arthritis	Decreased	Association	Human Urine	HMDB	15249323

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Firmicutes	34	Human ; Human feces; Human stool; Human urine	Indirect association between microbiota composition and metabolites measured in host biospecimen; Metabolic reconstruction
Bacteria	Proteobacteria	45	Human feces; Human sputum; Human unknown; Human	Metabolic reconstruction
Bacteria	Bacteroidetes	24	Human feces; Human appendix biopsy; Human ; Human stool	Metabolic reconstruction
Bacteria	Actinobacteria	10	Human feces	Metabolic reconstruction
Bacteria	Fusobacteria	2	Human feces	Metabolic reconstruction
Archaea	Euryarchaeota	1		Metabolic reconstruction
Bacteria	Planctomycetes	1	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified									HMDB
Human Blood	Detected and Quantified	20				uM	Newborn (0-30 days old)	Female	11-beta-hydroxylase deficiency	HMDB	8933406
Human Blood	Detected and Quantified			2.000	10.400	uM	Children (1-13 years old)	Both	11-beta-hydroxylase deficiency	HMDB	8933406
Human Blood	Detected and Quantified	5.493				uM	Adult (>18 years old)	Female	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency	HMDB	7951484
Human Blood	Detected and Quantified			42.0638	105.0238	uM	Newborn (0-30 days old)	Male	Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency	HMDB	27476613
Human Blood	Detected and Quantified	6.54	2.55			uM	Adult (>18 years old)	Female	Alzheimer's disease	HMDB	8478958
Human Blood	Detected and Quantified	<0.810				uM	Children (1-13 years old)	Female	Aromatase deficiency	HMDB	9177373
Human Blood	Detected and Quantified	0.0621				uM	Adult (>18 years old)	Female	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency	HMDB	26161337
Human Blood	Detected and Quantified	0.104				uM	Adolescent (13-18 years old)	Female	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency	HMDB	26161337
Human Blood	Detected and Quantified	9.8	1.3			uM	Adult (>18 years old)	Female	Hirsutism	HMDB	8187312
Human Blood	Detected and Quantified	<0.02				uM	Adult (>18 years old)	Female	Lipoid Adrenal Hyperplasia	HMDB	9077535
Human Blood	Detected and Quantified	<0.02				uM	Adolescent (13-18 years old)	Female	Lipoid Adrenal Hyperplasia	HMDB	9077535
Human Blood	Detected and Quantified	3.63	2.14			uM	Adult (>18 years old)	Female	Polycystic ovary syndrome (PCOS)	HMDB	15531511
Human Urine	Detected and Quantified	0.28	0.082			umol/mmol creatinine	Adult (>18 years old)	Both	Rheumatoid arthritis	HMDB	15249323
Human Urine	Detected and Quantified	0.84	0.51			umol/mmol creatinine	Adult (>18 years old)	Both	Rheumatoid arthritis	HMDB	15249323
Human Blood	Detected and Quantified			3.400	15	uM	Adult (>18 years old)	Male	X-linked ichthyosis	HMDB	3864567
Human Blood	Detected and Quantified	<0.500				uM	Not Specified	Both	Normal	HMDB	8933406
Human Blood	Detected and Quantified			0.950	11.669	uM	Adult (>18 years old)	Female	Normal	HMDB	26161337
Human Urine	Detected and Quantified	1.25		0.0026	2.52	umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	18501914
Human Urine	Detected and Quantified	1.34	0.23			umol/mmol creatinine	Adult (>18 years old)	Both	Normal	HMDB	15249323
Human Blood	Detected and Quantified	3.47	1.20			uM	Adult (>18 years old)	Female	Normal	HMDB	15531511
Human Blood	Detected and Quantified	4.5		1.4	8.2	uM	Adult (>18 years old)	Female	Normal	HMDB	8187312
Human Blood	Detected and Quantified			0	3.26	uM	Children (1 - <6 years old)	Both	Normal	HMDB	CALIPER Paediatric Reference Intervals
Human Blood	Detected and Quantified			0.27	4.34	uM	Children (6 - <9 years old)	Both	Normal	HMDB	CALIPER Paediatric Reference Intervals
Human Blood	Detected and Quantified			0.27	4.89	uM	Infant (6 months - <1 year old)	Both	Normal	HMDB	CALIPER Paediatric Reference Intervals
Human Blood	Detected and Quantified			0.81	16.28	uM	Infant (2 - <6 months old)	Both	Normal	HMDB	CALIPER Paediatric Reference Intervals
Human Blood	Detected and Quantified			0.81	7.60	uM	Children (9 - <13 years old)	Both	Normal	HMDB	CALIPER Paediatric Reference Intervals
Human Blood	Detected and Quantified			1.63	13.03	uM	Adolescent (13 - <16 years old)	Both	Normal	HMDB	CALIPER Paediatric Reference Intervals
Human Blood	Detected and Quantified			28.9	40.7	uM	Newborn (0-30 days old)	Both	Normal	HMDB	CALIPER Paediatric Reference Intervals
Human Blood	Detected and Quantified			3.53	16.01	uM	Adolescent (16 - <19 years old)	Male	Normal	HMDB	CALIPER Paediatric Reference Intervals
Human Blood	Detected and Quantified			4.07	16.01	uM	Adolescent (16 - <19 years old)	Female	Normal	HMDB	CALIPER Paediatric Reference Intervals
Human Blood	Detected and Quantified			0.950	1.167	uM	Adult (>18 years old)	Both	Normal	HMDB	Vancouver Coastal Health Lab (http://www.vch.ca/Locations-Services/result?res_id=601)
Human Kidney	Detected but not Quantified						Not Specified	Not Specified	Normal	HMDB	34986597
Human Liver	Detected but not Quantified						Not Specified	Not Specified	Normal	HMDB	34986597
Human Placenta	Detected but not Quantified						Not Specified	Not Specified	Normal	HMDB	34986597
Human Prostate	Detected but not Quantified						Not Specified	Not Specified	Normal	HMDB	34986597
Human Blood	Detected but not Quantified						Adult (>18 years old)	Female	Normal	HMDB	22944140
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
Human Urine	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	32966057
Human Blood	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	32966057

External Links

HMDB ID

HMDB0001032

DrugBank ID

DB05804

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022381

KNApSAcK ID

Not Available

Chemspider ID

12074

KEGG Compound ID

C04555

BioCyc ID

DEHYDRO-EPIANDROSTERONE-SULFATE

BiGG ID

44038

Wikipedia Link

Dehydroepiandrosterone_sulfate

METLIN ID

4095

PubChem Compound

12594

PDB ID

Not Available

ChEBI ID

16814

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Gordon GB, Bush TL, Helzlsouer KJ, Miller SR, Comstock GW: Relationship of serum levels of dehydroepiandrosterone and dehydroepiandrosterone sulfate to the risk of developing postmenopausal breast cancer. Cancer Res. 1990 Jul 1;50(13):3859-62. [PubMed:2141293 ]
Milewich L, Sontheimer RD, Herndon JH Jr: Steroid sulfatase activity in epidermis of acne-prone and non-acne-prone skin of patients with acne vulgaris. Arch Dermatol. 1990 Oct;126(10):1312-4. [PubMed:2145810 ]
Zappulla F, Ventura D, Capelli M, Cassio A, Balsamo A, Frejaville E, Bolelli G, Cacciari E: Gonadal and adrenal secretion of dehydroepiandrosterone sulfate in prepubertal and pubertal subjects. J Endocrinol Invest. 1981 Apr-Jun;4(2):197-202. doi: 10.1007/BF03350452. [PubMed:6268694 ]
Gu H, Li Y, Rong L: [The effect of sodium prasterone sulfate on lactation]. Zhonghua Fu Chan Ke Za Zhi. 1995 Apr;30(4):197-9. [PubMed:7664601 ]
Jaquish CE, Blangero J, Haffner SM, Stern MP, Maccluer JW: Quantitative genetics of dehydroepiandrosterone sulfate and its relation to possible cardiovascular disease risk factors in Mexican Americans. Hum Hered. 1996 Nov-Dec;46(6):301-9. doi: 10.1159/000154368. [PubMed:8956025 ]
De Pergola G, Zamboni M, Sciaraffia M, Turcato E, Pannacciulli N, Armellini F, Giorgino F, Perrini S, Bosello O, Giorgino R: Body fat accumulation is possibly responsible for lower dehydroepiandrosterone circulating levels in premenopausal obese women. Int J Obes Relat Metab Disord. 1996 Dec;20(12):1105-10. [PubMed:8968856 ]
Coulter CL, Jaffe RB: Functional maturation of the primate fetal adrenal in vivo: 3. Specific zonal localization and developmental regulation of CYP21A2 (P450c21) and CYP11B1/CYP11B2 (P450c11/aldosterone synthase) lead to integrated concept of zonal and temporal steroid biosynthesis. Endocrinology. 1998 Dec;139(12):5144-50. doi: 10.1210/endo.139.12.6333. [PubMed:9832454 ]
Roberts E: The importance of being dehydroepiandrosterone sulfate (in the blood of primates): a longer and healthier life? Biochem Pharmacol. 1999 Feb 15;57(4):329-46. doi: 10.1016/s0006-2952(98)00246-9. [PubMed:9933021 ]
Ankarberg C, Norjavaara E: Diurnal rhythm of testosterone secretion before and throughout puberty in healthy girls: correlation with 17beta-estradiol and dehydroepiandrosterone sulfate. J Clin Endocrinol Metab. 1999 Mar;84(3):975-84. doi: 10.1210/jcem.84.3.5524. [PubMed:10084582 ]
Benvenga S, Smedile G, Lo Giudice F, Trimarchi F: Testicular adrenal rests: evidence for luteinizing hormone receptors and for distinct types of testicular nodules differing for their autonomization. Eur J Endocrinol. 1999 Sep;141(3):231-7. doi: 10.1530/eje.0.1410231. [PubMed:10474120 ]
Wang HS, Wang TH, Soong YK: Low dose flutamide in the treatment of acne vulgaris in women with or without oligomenorrhea or amenorrhea. Changgeng Yi Xue Za Zhi. 1999 Sep;22(3):423-32. [PubMed:10584414 ]
Ibanez L, Potau N, Marcos MV, de Zegher F: Exaggerated adrenarche and hyperinsulinism in adolescent girls born small for gestational age. J Clin Endocrinol Metab. 1999 Dec;84(12):4739-41. doi: 10.1210/jcem.84.12.6341. [PubMed:10599744 ]
Chang HJ, Shi R, Rehse P, Lin SX: Identifying androsterone (ADT) as a cognate substrate for human dehydroepiandrosterone sulfotransferase (DHEA-ST) important for steroid homeostasis: structure of the enzyme-ADT complex. J Biol Chem. 2004 Jan 23;279(4):2689-96. doi: 10.1074/jbc.M310446200. Epub 2003 Oct 21. [PubMed:14573603 ]
Zouboulis CC, Degitz K: Androgen action on human skin -- from basic research to clinical significance. Exp Dermatol. 2004;13 Suppl 4:5-10. doi: 10.1111/j.1600-0625.2004.00255.x. [PubMed:15507105 ]
Rainey WE, Rehman KS, Carr BR: The human fetal adrenal: making adrenal androgens for placental estrogens. Semin Reprod Med. 2004 Nov;22(4):327-36. doi: 10.1055/s-2004-861549. [PubMed:15635500 ]
Clauss SB, Holmes KW, Hopkins P, Stein E, Cho M, Tate A, Johnson-Levonas AO, Kwiterovich PO: Efficacy and safety of lovastatin therapy in adolescent girls with heterozygous familial hypercholesterolemia. Pediatrics. 2005 Sep;116(3):682-8. doi: 10.1542/peds.2004-2090. [PubMed:16140708 ]
Sipila S, Heikkinen E, Cheng S, Suominen H, Saari P, Kovanen V, Alen M, Rantanen T: Endogenous hormones, muscle strength, and risk of fall-related fractures in older women. J Gerontol A Biol Sci Med Sci. 2006 Jan;61(1):92-6. doi: 10.1093/gerona/61.1.92. [PubMed:16456199 ]
Dalla Valle L, Toffolo V, Nardi A, Fiore C, Bernante P, Di Liddo R, Parnigotto PP, Colombo L: Tissue-specific transcriptional initiation and activity of steroid sulfatase complementing dehydroepiandrosterone sulfate uptake and intracrine steroid activations in human adipose tissue. J Endocrinol. 2006 Jul;190(1):129-39. doi: 10.1677/joe.1.06811. [PubMed:16837617 ]
Cutolo M, Sulli A, Capellino S, Villaggio B, Montagna P, Pizzorni C, Paolino S, Seriolo B, Felli L, Straub RH: Anti-TNF and sex hormones. Ann N Y Acad Sci. 2006 Jun;1069:391-400. doi: 10.1196/annals.1351.037. [PubMed:16855166 ]
Cappola AR, Xue QL, Walston JD, Leng SX, Ferrucci L, Guralnik J, Fried LP: DHEAS levels and mortality in disabled older women: the Women's Health and Aging Study I. J Gerontol A Biol Sci Med Sci. 2006 Sep;61(9):957-62. doi: 10.1093/gerona/61.9.957. [PubMed:16960027 ]
Sreekumar A, Poisson LM, Rajendiran TM, Khan AP, Cao Q, Yu J, Laxman B, Mehra R, Lonigro RJ, Li Y, Nyati MK, Ahsan A, Kalyana-Sundaram S, Han B, Cao X, Byun J, Omenn GS, Ghosh D, Pennathur S, Alexander DC, Berger A, Shuster JR, Wei JT, Varambally S, Beecher C, Chinnaiyan AM: Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression. Nature. 2009 Feb 12;457(7231):910-4. doi: 10.1038/nature07762. [PubMed:19212411 ]
Elshenawy S, Pinney SE, Stuart T, Doulias PT, Zura G, Parry S, Elovitz MA, Bennett MJ, Bansal A, Strauss JF 3rd, Ischiropoulos H, Simmons RA: The Metabolomic Signature of the Placenta in Spontaneous Preterm Birth. Int J Mol Sci. 2020 Feb 4;21(3). pii: ijms21031043. doi: 10.3390/ijms21031043. [PubMed:32033212 ]

Showing metabocard for Dehydroepiandrosterone sulfate (MMDBc0000561)

MOL for #<Metabolite:0x000055c79c481c50>

3D MOL for #<Metabolite:0x000055c79c481c50>

3D SDF for #<Metabolite:0x000055c79c481c50>

3D-SDF for #<Metabolite:0x000055c79c481c50>

PDB for #<Metabolite:0x000055c79c481c50>

3D PDB for #<Metabolite:0x000055c79c481c50>

SMILES for #<Metabolite:0x000055c79c481c50>

INCHI for #<Metabolite:0x000055c79c481c50>

Structure for #<Metabolite:0x000055c79c481c50>

3D Structure for #<Metabolite:0x000055c79c481c50>