Bexlosteride
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Revision as of 07:45, 18 April 2010 by حسن علي البط (Talk) (Adding category Category:Benzoquinolines (using HotCat))
File:Bexlosteride pic.png | |
Systematic (IUPAC) name | |
---|---|
(4aS,10bR)-8-chloro-4-methyl-1,2,4a,5,6,10b-hexahydrobenzo[f]quinolin-
3-one | |
Clinical data | |
Routes of administration | Oral |
Legal status | |
Legal status |
|
Identifiers | |
CAS Number | 202189-78-4 |
ATC code | none |
PubChem | CID 166562 |
Chemical data | |
Formula | C14H16ClNO |
Molar mass | 249.73594 g/mol[[Script error: No such module "String".]] |
Script error: No such module "collapsible list". |
Bexlosteride (LY-191,704) is a potent and noncompetitive inhibitor of the enzyme 5α-reductase related to finasteride and dutasteride.[1][2] It is selective for the type I isoform of the enzyme.[1] It was never marketed.
See also
References
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- ↑ 1.0 1.1 Chang, Chawnshang (2002). Androgens and androgen receptor : mechanisms, functions, and clinical application. Boston: Kluwer Academic Publishers. ISBN 1-4020-7188-4.
- ↑ Lednicer, Daniel (2008). Strategies for Organic Drug Synthesis and Design. New York: Wiley-Interscience. ISBN 0-470-19039-6.
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- 5-alpha-reductase inhibitors
- Lactams
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