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53-00-9

Weight	304.43 g/mol
Formula	C₁₉H₂₈O₃
Hydrogen Acceptors	3
Hydrogen Donors	2
Aromatic Rings	0
Rotatable Bonds	0

53-00-9 (53-00-9)

Score: #193 in Environmental science , #4118 in Biology , #5188 in Chemistry

Alcohol · Antiestrogen · Antiglucocorticoid · Drugs acting on the genito-urinary system · Estrogen · Hormonal agent · Ketone · Organic compound · Sex hormone · Systemic hormonal preparation

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Most-cited Publications

Book reviewManaged grassland. Analytical studies: by R.W. Snaydon (Editor). Volume 17B, Ecosystems of the World, Elsevier, Amsterdam, 1987, xiv + 286 pp., 53 tables, 93 figures, hardcover, Dfl. 300.00, ISBN: 0-444-42565-9 (Agriculture, Ecosystems & Environment, 1988)
Transformation or organometallics into common and exotic materials: Design and activation. R M Laine, Martinus Nijhof, Dordrecht, Boston, Lancaster, 1988, 306 pp. Price $96.00 (US); 53 (UK); 175.00 Dfl ISBN 9 024 73661 7 (Applied Organometallic Chemistry, 1989)
Collared Urns of the Bronze Age in Great Britain and Ireland . By Ian H. Longworth. (Gulbenkian Archaeological Series.) 30.5 23 cm. Pp. xiv + 338, 53 figs.+ 246 pls. Cambridge: Cambridge University Press, 1984. ISBN 0-521-08596-9. 85.00. (The Antiquaries Journal, 1985)
U. Frstner & G. T. W. Wittmann 1979. Metal Pollution in the Aquatic Environment. xiv + 486 pp., 102 figs, 94 tables. Berlin, Heidelberg, New York: Springer-Verlag. Price DM 98.00; U.S. $53.90. ISBN 3 540 09307 9. (Geological Magazine, 1980)
St Magnus Cathedral and Orkney's Twelfth-Century Renaissance . Edited by Barbara E. Crawford. 255 185mm. Pp. xviii + 283, 28 figs., 53 pls. incl. 11 col. Aberdeen: Aberdeen University Press, 1988. ISBN 0-08-036580-9. 2500. (The Antiquaries Journal, 1989)
The Archaeology of York. Vol. 17, fasc. 5. Textiles, Cordage and Raw Fibre from 1622 Coppergate. By Penelope Walton. 241 184mm. Pp. 172, 53 figs. 34 pls., 1 microfiche. London: Council for British Archaeology for the York Archaeological Trust, 1989. ISBN 0-906780-79-9. 1800 (p/b). (The Antiquaries Journal, 1989)

Areas of Application

Safety

Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more.

Alternate Names

SMILES

CC12CCC3C(C1CCC2=O)C(C=C4C3(CCC(C4)O)C)O
InChIKey

OLPSAOWBSPXZEA-UHFFFAOYSA-N

External Links

Pubchem - 53-00-9
Wikipedia - 7-hydroxydehydroepiandrosterone
7-Hydroxydehydroepiandrosterone (7-hydroxy-DHEA; 7-OH-DHEA), also known as 3,7-dihydroxyandrost-4-ene-17-one, is an endogenous, naturally occurring steroid and a major metabolite of dehydroepiandrosterone (DHEA) that is formed by CYP7B1 (steroid 7-hydroxylase) in tissues such as the prostate gland and by CYP3A4 in the liver. The major metabolic pathway of DHEA outside the liver is via 7-hydroxylation into 7-OH-DHEA and 7-OH-DHEA. 7-OH-DHEA has weak estrogenic activity, selectively activating the estrogen receptor ER.