The Wayback Machine - https://web.archive.org/web/20120130074428/http://en.wikipedia.org/wiki/KML-010

KML-010

From Wikipedia, the free encyclopedia
Jump to: navigation, search
KML-010
Systematic (IUPAC) name
8-[4-(4-fluorophenyl)-4-oxobutyl]-1-methyl-1,3,8-triazaspiro[4.5]decan-4-one
Clinical data
Pregnancy cat.  ?
Legal status  ?
Identifiers
ATC code  ?
PubChem CID 10404584
Chemical data
Formula C18H24FN3O2 
Mol. mass 333.400 g/mol
SMILES eMolecules & PubChem
 YesY(what is this?)  (verify)

KML-010 is a drug derived from spiperone. It functions as a highly selective 5-HT2A receptor antagonist, with negligible affinity for the 5-HT1A or 5-HT2C receptors, and over 400-fold lower affinity for the D2 receptor in comparison to spiperone.[1]

[edit] See also

[edit] References

  1. ^ Glennon RA, Metwally K, Dukat M, Ismaiel AM, De los Angeles J, Herndon J, Teitler M, Khorana N (June 2002). "Ketanserin and spiperone as templates for novel serotonin 5-HT(2A) antagonists". Current Topics in Medicinal Chemistry 2 (6): 539–58. doi:10.2174/1568026023393787. PMID 12052193. 


Personal tools
Namespaces
Variants
Actions
Navigation
Interaction
Toolbox
Print/export
Morty Proxy This is a proxified and sanitized view of the page, visit original site.