Indiplon

From Wikipedia, the free encyclopedia

ATC code
  • none
Elimination half-life1.5–1.8 hours
Indiplon
Clinical data
Routes of
administration
Oral
ATC code
  • none
Pharmacokinetic data
Elimination half-life1.5–1.8 hours
Identifiers
  • N-methyl-N-[3-[3-(thiophene-2-carbonyl)
    pyrazolo[5,1-b]pyrimidin-7-yl]phenyl]acetamide
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.133.676 Edit this at Wikidata
Chemical and physical data
FormulaC20H16N4O2S
Molar mass376.43 g·mol−1
3D model (JSmol)
  • O=C(C1=CC=CS1)C2=C3N=CC=C(C4=CC(N(C)C(C)=O)=CC=C4)N3N=C2
  • InChI=1S/C20H16N4O2S/c1-13(25)23(2)15-6-3-5-14(11-15)17-8-9-21-20-16(12-22-24(17)20)19(26)18-7-4-10-27-18/h3-12H,1-2H3 checkY
  • Key:CBIAWPMZSFFRGN-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Indiplon (INN and USAN) is an unmarketed nonbenzodiazepine, hypnotic sedative that was developed in two formulations—an immediate-release formulation for sleep onset, and a modified-release (also called controlled-release or extended-release) version for sleep maintenance.

Pharmacodynamics

Indiplon works by enhancing the action of the inhibitory neurotransmitter GABA, like most other nonbenzodiazepine sedatives. It primarily binds to benzodiazepine sites on α1 subunit-containing GABAA receptors in the brain.[1]

Pharmacokinetics

Indiplon has a short elimination half-life of 1.5 to 1.8 hours in young and elderly subjects, respectively.[2]

Chemistry

Indiplon is a pyrazolopyrimidine related to the nonbenzodiazepine hypnotic zaleplon.[3]

History

References

Related Articles

Wikiwand AI