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Thioperamide

From Wikipedia, the free encyclopedia

Thioperamide
Clinical data
ATC code
  • none
Identifiers
  • N-Cyclohexyl-4-(1H-imidazol-4-yl)piperidine-1-carbothioamide
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC15H24N4S
Molar mass292.45 g·mol−1
3D model (JSmol)
  • S=C(NC1CCCCC1)N3CCC(c2cnc[nH]2)CC3
  • InChI=1S/C15H24N4S/c20-15(18-13-4-2-1-3-5-13)19-8-6-12(7-9-19)14-10-16-11-17-14/h10-13H,1-9H2,(H,16,17)(H,18,20) checkY
  • Key:QKDDJDBFONZGBW-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Thioperamide is a potent HRH4 antagonist and selective HRH3 antagonist capable of crossing the blood–brain barrier.[1] It was used by Jean-Charles Schwartz in his early experiments regarding the H3 receptor.[2] Thioperamide was found to be an antagonist of histamine autoreceptors, which negatively regulate the release of histamine. The drug enhances the activity of histaminergic neurons by blocking autoreceptors, leading to greater release of histamine.

Its action on H3 receptors is thought to promote wakefulness and improve memory consolidation.

YouTube Encyclopedic

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  • Histamine antagonist

Transcription

See also

References

  1. ^ "Thioperamide". IUPHAR/BPS Guide to Pharmacology.
  2. ^ Schwartz JC (June 2011). "The histamine H3 receptor: from discovery to clinical trials with pitolisant". British Journal of Pharmacology. 163 (4): 713–21. doi:10.1111/j.1476-5381.2011.01286.x. PMC 3111674. PMID 21615387.


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This page was last edited on 3 October 2023, at 16:47
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