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Cerlapirdine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Cerlapirdine
Clinical data
ATC code
  • none
Legal status
Legal status
  • Investigational
Identifiers
  • N,N-dimethyl-3-[(3-naphthalen-1-ylsulfonyl-2H-indazol-5-yl)oxy]propan-1-amine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC22H23N3O3S
Molar mass409.50 g·mol−1
3D model (JSmol)
  • CN(C)CCCOc4ccc3[nH]nc(S(=O)(=O)c1cccc2ccccc12)c3c4
  • InChI=1S/C22H23N3O3S/c1-25(2)13-6-14-28-17-11-12-20-19(15-17)22(24-23-20)29(26,27)21-10-5-8-16-7-3-4-9-18(16)21/h3-5,7-12,15H,6,13-14H2,1-2H3,(H,23,24)
  • Key:NXQGEDVQXVTCDA-UHFFFAOYSA-N

Cerlapirdine (USAN;SAM-531,WAY-262,531,PF-05212365) is adrug which was under development byWyeth/Pfizer for the treatment ofcognitive disorders associated withAlzheimer's disease andschizophrenia.[1] In aphase IIclinical trial it demonstrated a trend toward efficacy along with a goodside effect profile and no incidence of serious adverse events,[2] but no furtherdevelopment has occurred since 2011.[3]

It exerts its effects by acting as aselective5-HT6 receptorantagonist.[1]

See also

[edit]

References

[edit]
  1. ^abCodony X, Vela JM, Ramírez MJ (February 2011). "5-HT(6) receptor and cognition".Current Opinion in Pharmacology.11 (1):94–100.doi:10.1016/j.coph.2011.01.004.hdl:10171/18451.PMID 21330210.
  2. ^Franco Borsini (2011).International review of neurobiology: Pharmacology of 5-HT6 receptors. Part 2. Academic Press. p. 5.ISBN 978-0-12-385902-0. Retrieved25 October 2011.
  3. ^Drug Profile: Cerlapirdine
Psychoanaleptics: Anti-dementia agents (ATC codeN06D and others)
AChE inhibitor medications
Other medications
ExperimentalBACE inhibitors
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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