Thioperamide

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Thioperamide
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Clinical data
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  • none
Identifiers
  • N-Cyclohexyl-4-(1H-imidazol-4-yl)piperidine-1-carbothioamide
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Chemical and physical data
FormulaC15H24N4S
Molar mass292.45 g·mol−1
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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.

See also

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content."Thioperamide". IUPHAR/BPS Guide to Pharmacology.
  2. ^ Page Module:Citation/CS1/styles.css has no content.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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