Chemistry:Lapisteride

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Short description: Chemical compound
Lapisteride
Lapisteride.png
Clinical data
Routes of
administration
Oral[1]
ATC code
  • None
Legal status
Legal status
  • In general: non-regulated
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
FormulaC29H40N2O3
Molar mass464.650 g·mol−1
3D model (JSmol)
  (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

References

  1. "Solid phase transition of CS-891 enantiotropes during grinding". International Journal of Pharmaceutics 255 (1–2): 69–79. April 2003. doi:10.1016/S0378-5173(03)00084-X. PMID 12672603. 
  2. 2.0 2.1 "The novel drug CS-891 inhibits 5alpha-reductase activity in freshly isolated dermal papilla of human hair follicles". European Journal of Dermatology 10 (8): 593–595. December 2000. PMID 11125319. http://www.jle.com/medline.md?issn=1167-1122&vol=10&iss=8&page=593. 
  3. Bernan; British Pharmacopoeia Commission (February 2002). British Approved Names 2002. The Stationery Office. pp. 157. ISBN 978-0-11-322558-3. https://books.google.com/books?id=zruxjioUFngC&pg=PA157. Retrieved 17 November 2011. 

{{Navbox

| name = Drugs used in benign prostatic hypertrophy
| title = Drugs used in [[Medicine:Benign prostatic hyperpbenign prostatic hyperplasia (G04C)
| state = collapsed
| listclass = hlist
| group1 = 5α-Reductase inhibitors
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| group2 = Alpha-1 blockers
| list2 =
| group3 = Steroidal antiandrogens
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| group4 = Herbal products
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| group5 = Others
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}}