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KML-010

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
KML-010
Identifiers
  • 8-[4-(4-fluorophenyl)-4-oxobutyl]-1-methyl-1,3,8-triazaspiro[4.5]decan-4-one
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H24FN3O2
Molar mass333.407 g·mol−1
3D model (JSmol)
  • O=C1NCN(C)C1(CC2)CCN2CCCC(=O)c(cc3)ccc3F
  • InChI=1S/C18H24FN3O2/c1-21-13-20-17(24)18(21)8-11-22(12-9-18)10-2-3-16(23)14-4-6-15(19)7-5-14/h4-7H,2-3,8-13H2,1H3,(H,20,24)
  • Key:GRADLHIYNHRBCW-UHFFFAOYSA-N
  (verify)

KML-010 is adrug derived fromspiperone. It functions as a highly selective5-HT2A receptorantagonist, with negligible affinity for the5-HT1A or5-HT2C receptors, and over 400-fold lower affinity for theD2 receptor in comparison tospiperone.[1]

See also

[edit]

References

[edit]
  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.
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7


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