Revospirone

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Revospirone
File:Revospirone.png
Systematic (IUPAC) name
1,1-dioxo-2-[3-(4-pyrimidin-2-ylpiperazin-1-yl)propyl]-1,2-benzothiazol-3-one
Clinical data
Routes of
administration		 Oral
Legal status
Legal status
  • Uncontrolled
Identifiers
CAS Number 95847-87-3
ATC code none
PubChem CID 72024
ChemSpider 65018
Chemical data
Formula C18H21N5O3S
Molar mass 387.46[[Script error: No such module "String".]]
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Revospirone (BAY-VQ-7,813) is a selective 5-HT1A receptor partial agonist of the azapirone class.[1] As with buspirone, gepirone, ipsapirone, and tandospirone, 1-PP is an active metabolite of revospirone; hence, it also has some α2-adrenergic receptor antagonist properties.[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 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
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