Bexlosteride
Clinical data | |
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Routes of administration | Oral |
ATC code | none |
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Identifiers | |
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Synonyms | LY 300502 |
CAS Number | 148905-78-6 |
PubChem (CID) | 166562 |
ChemSpider | 145762 |
UNII | 36X732P4P0 |
ChEMBL | CHEMBL24955 |
Chemical and physical data | |
Formula | C14H16ClNO |
Molar mass | 249.73594 g/mol |
3D model (Jmol) | Interactive image |
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Bexlosteride 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 advanced to Phase III clinical trials, but development was halted at that stage, and it was never marketed.[3][4]
See also
References
- 1 2 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.
- ↑ "Drug Profile: Bexlosteride". Adis Insight.
- ↑ Reaxys entry for bexlosteride: Reaxys Registry Number: 6635310
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