16α-Hydroxy-DHEA sulfate - Misplaced Pages

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16α-Hydroxy-DHEA sulfate
Names

IUPAC name 16α-Hydroxy-17-oxoandrost-5-en-3β-yl hydrogen sulfate
Systematic IUPAC name (2R,3aS,3bR,7S,9aR,9bS,11aS)-2-Hydroxy-9a,11a-dimethyl-1-oxo-2,3,3a,3b,4,6,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-cyclopentaphenanthren-7-yl hydrogen sulfate
Other names 16α-Hydroxy-17-oxoandrost-5-en-3β-yl sulfate; 16α-OH-DHEA-S
Identifiers
CAS Number	4873-65-8
3D model (JSmol)	Interactive image
ChEBI	CHEBI:87538
ChemSpider	24850136
PubChem CID	20848950
CompTox Dashboard (EPA)	DTXSID901033144
InChI InChI=1S/C19H28O6S/c1-18-7-5-12(25-26(22,23)24)9-11(18)3-4-13-14(18)6-8-19(2)15(13)10-16(20)17(19)21/h3,12-16,20H,4-10H2,1-2H3,(H,22,23,24)/t12-,13+,14-,15-,16+,18-,19-/m0/s1Key: ALBNSVAJDFJRKQ-DNKQKWOHSA-N
SMILES C12CC(CC1=CC32CC4(3C(C4=O)O)C)OS(=O)(=O)O
Properties
Chemical formula	C₁₉H₂₈O₆S
Molar mass	384.49 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

16α-Hydroxydehydroepiandrosterone sulfate (16α-OH-DHEA-S), also known as 16α-hydroxy-17-oxoandrost-5-en-3β-yl sulfate, is an endogenous, naturally occurring steroid and a metabolic intermediate in the production of estriol from dehydroepiandrosterone (DHEA) during pregnancy. It is the C3β sulfate ester of 16α-hydroxy-DHEA.

References

Jerome F. Strauss, III; Robert L. Barbieri (13 September 2013). Yen and Jaffe's Reproductive Endocrinology. Elsevier Health Sciences. pp. 256–. ISBN 978-1-4557-2758-2.
Hiroshi Yamazaki (23 June 2014). Fifty Years of Cytochrome P450 Research. Springer. pp. 385–. ISBN 978-4-431-54992-5.
Mike S. Lee (8 May 2012). Mass Spectrometry Handbook. John Wiley & Sons. pp. 320–. ISBN 978-0-470-53673-5.
Shlomo Melmed; Kenneth S. Polonsky; P. Reed Larsen; Henry M. Kronenberg (30 November 2015). Williams Textbook of Endocrinology. Elsevier Health Sciences. pp. 839–. ISBN 978-0-323-29738-7.

Others

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