Lapisteride
Systematic (IUPAC) name | |
---|---|
N-[1-(4-methoxyphenyl)-1-methylethyl]-3-oxo-4-aza-5α-androst-1-ene-17β-carboxamide | |
Clinical data | |
| |
Oral[1] | |
Identifiers | |
142139-60-4 | |
None | |
PubChem | CID 9847295 |
ChemSpider | 8023009 |
UNII | T50SJ23G82 |
Chemical data | |
Formula | C29H40N2O3 |
464.6395 g/mol | |
SMILES
| |
| |
(what is this?) (verify) |
Lapisteride (INN; CS-891) is a dual inhibitor of both isoforms of the enzyme 5α-reductase.[2] It was under investigation for the treatment of benign prostatic hyperplasia (BPH) and androgenic alopecia,[2][3] but was never marketed.
See also
- 5α-reductase inhibitor
References
- ↑ Yada S, Ohya M, Ohuchi Y et al. (April 2003). "Solid phase transition of CS-891 enantiotropes during grinding". International Journal of Pharmaceutics 255 (1-2): 69–79. doi:10.1016/S0378-5173(03)00084-X. PMID 12672603.
- ↑ 2.0 2.1 Niiyama S, Kojima K, Hamada T, Happle R, Hoffmann R (December 2000). "The novel drug CS-891 inhibits 5alpha-reductase activity in freshly isolated dermal papilla of human hair follicles". European Journal of Dermatology 10 (8): 593–5. PMID 11125319.
- ↑ Bernan; British Pharmacopoeia Commission (February 2002). British Approved Names 2002. The Stationery Office. p. 157. ISBN 978-0-11-322558-3. Retrieved 17 November 2011.
|
|