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Hydromadinone

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Hydromadinone
Clinical data
ATC code
  • None
Identifiers
  • 6α-Chloro-17α-hydroxypregn-4-ene-3,20-dione
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC21H29ClO3
Molar mass364.91 g·mol−1
3D model (JSmol)
  • CC(=O)[C@]1(CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C[C@@H](C4=CC(=O)CC[C@]34C)Cl)C)O
  • InChI=1S/C21H29ClO3/c1-12(23)21(25)9-6-16-14-11-18(22)17-10-13(24)4-7-19(17,2)15(14)5-8-20(16,21)3/h10,14-16,18,25H,4-9,11H2,1-3H3/t14-,15+,16+,18+,19-,20+,21+/m1/s1
  • Key:IMUIZZGKYILUHZ-SCUQKFFVSA-N

Hydromadinone (INN), also known as6α-chloro-17α-hydroxyprogesterone, is asteroidalprogestin of the17α-hydroxyprogesterone group which was patented in 1967 but was never marketed.[1] The C17αacetateester of hydromadinone,hydromadinone acetate, also exists, but similarly was never marketed.[1]

See also

[edit]

References

[edit]
  1. ^abGanellin CR, Triggle DJ (21 November 1996).Dictionary of Pharmacological Agents. CRC Press. p. 1037.ISBN 978-0-412-46630-4.
PRTooltip Progesterone receptor
Agonists
Mixed
(SPRMsTooltip Selective progesterone receptor modulators)
Antagonists
mPRTooltip Membrane progesterone receptor
(PAQRTooltip Progestin and adipoQ receptor)
Agonists
Antagonists

This article about apregnanes is astub. You can help Wikipedia byexpanding it.

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