ZM-182345
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Revision as of 02:30, 3 December 2020 by Monkbot (talk | contribs) (Task 18 (cosmetic): eval 2 templates: del empty params (1×);)
Pharmaceutical compound
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PubChem CID | |
CompTox Dashboard (EPA) | |
Chemical and physical data | |
Formula | C19H16F6N2O4 |
Molar mass | 450.337 g·mol−1 |
3D model (JSmol) | |
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ZM-182345 is a nonsteroidal progestin that was never marketed.[1][2] It was derived from structural modification of the nonsteroidal antiandrogen hydroxyflutamide.[1][2] ZM-182345 was found to be at least as potent as progesterone as a progestogen in animals but to also possess androgenic activity.[1]
References
- ^ a b c Dukes M, Furr BJ, Hughes LR, Tucker H, Woodburn JR (2000). "Nonsteroidal progestins and antiprogestins related to flutamide". Steroids. 65 (10–11): 725–31. doi:10.1016/s0039-128x(00)00179-3. PMID 11108883. S2CID 9749394.
- ^ a b Eckhard Ottow; Hilmar Weinmann (8 September 2008). Nuclear Receptors as Drug Targets. John Wiley & Sons. pp. 209–. ISBN 978-3-527-62330-3.
PRTooltip Progesterone receptor |
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mPRTooltip Membrane progesterone receptor (PAQRTooltip Progestin and adipoQ receptor) |
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