Ipsapirone

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Ipsapirone
File:Ipsapirone.svg
Systematic (IUPAC) name
9,9-dioxo-8-[4-(4-pyrimidin-2-ylpiperazin-1-yl)butyl]-
9λ6-thia-8-azabicyclo[4.3.0]nona-1,3,5-trien-7-one
Clinical data
Routes of
administration		 Oral
Legal status
Legal status
  • Uncontrolled
Pharmacokinetic data
Biological half-life 1.3-2.7 hours
Identifiers
CAS Number 95847-70-4
ATC code none
PubChem CID 56971
IUPHAR/BPS 42
Chemical data
Formula C19H23N5O3S
Molar mass 401.484 g/mol[[Script error: No such module "String".]]
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Ipsapirone is a selective 5-HT1A receptor partial agonist of the piperazine and azapirone chemical classes.[1] It has antidepressant and anxiolytic effects.[1]

See also

References

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GABAA PAMs
Others
α2δ VDCC Blockers
5-HT1A Agonists
Azapirones: Buspirone • Gepirone • Tandospirone; Others: Flesinoxan • Oxaflozane
H1 Antagonists
Diphenylmethanes: Captodiame • Hydroxyzine; Others: Brompheniramine • Chlorpheniramine • Pheniramine
CRH1 Antagonists
NK2 Antagonists
MCH1 antagonists
mGluR2/3 Agonists
mGluR5 NAMs
TSPO agonists
σ1 agonists
Others

M: PSO/PSI

dsrd (o, p, m, p, a, d, s), sysi/epon, spvo

proc, drug(N5A/5B/5C/6A/6B/6D)


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  1. ↑ 1.0 1.1 Fanelli RJ, Schuurman T, Glaser T, Traber J (1990). "Ipsapirone: a novel anxiolytic and selective 5-HT1A receptor ligand". Progress in clinical and biological research. 361: 461–7. PMID 1981264. 
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