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Zalospirone

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Zalospirone
File:Zalospirone.svg
Systematic (IUPAC) name
(3aα,4α,4aβ,6aβ,7α,7aα)-hexahydro-2-(4-(4-(2-pyrimidinyl)-1-piperazinyl)butyl)-4,7-etheno-1H-cyclobut(f)isoindole-1,3(2H)-dione
Clinical data
  • Uncontrolled
Oral
Pharmacokinetic data
Half-life 1-4 hours
Identifiers
114298-18-9
None
PubChem CID 163925
IUPHAR ligand 58
ChemSpider 143768
UNII 0449O95Z1J 7pxY
Chemical data
Formula C24H29N5O2
419.519 g/mol
 14pxY (what is this?)  (verify)

Zalospirone (WY-47,846) is a selective 5-HT1A partial agonist of the azapirone chemical class.[1][2] It was found to be effective in the treatment of anxiety and depression in clinical trials, but a high proportion of subjects dropped out due to side effects and development was subsequently never completed.[3]

See also

References

  1. ^ Gleeson, S; Barrett, JE (1990). "5-HT1A agonist effects on punished responding of squirrel monkeys". Pharmacology, Biochemistry, and Behavior 37 (2): 335–7. PMID 1981937. doi:10.1016/0091-3057(90)90344-H. 
  2. ^ Singh, A; Lucki, I (1993). "Antidepressant-like activity of compounds with varying efficacy at 5-HT1A receptors". Neuropharmacology 32 (4): 331–40. PMID 8497336. doi:10.1016/0028-3908(93)90153-T. 
  3. ^ Rickels, K; Derivan, A; Kunz, N; Pallay, A; Schweizer, E (1996). "Zalospirone in major depression: a placebo-controlled multicenter study". Journal of Clinical Psychopharmacology 16 (3): 212–7. PMID 8784652. doi:10.1097/00004714-199606000-00004. 


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