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Pitolisant-d10

CAT:
804-HY-12199S
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  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Pitolisant-d10 - image 1

Pitolisant-d10

  • UNSPSC Description: Pitolisant-d10 (Tiprolisant-d10) is deuterium labeled Pitolisant. Pitolisant is a potent and selective nonimidazole inverse agonist at the recombinant human histamine H3 receptor (Ki=0.16 nM)[1].
  • Target Antigen: Histamine Receptor; Isotope-Labeled Compounds
  • Type: Isotope-Labeled Compounds
  • Related Pathways: GPCR/G Protein;Immunology/Inflammation;Neuronal Signaling;Others
  • Field of Research: Neurological Disease;Endocrinology
  • Smiles: [2H]C1([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])N1CCCOCCCC2=CC=C(Cl)C=C2
  • Molecular Weight: 305.91
  • References & Citations: [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.|[2]Uguen M, et al. Preclinical evaluation of the abuse potential of Pitolisant, a histamine H? receptor inverse agonist/antagonist compared with Modafinil. Br J Pharmacol. 2013 Jun;169(3):632-44.|[3]Dudek M, et al. H3 histamine receptor antagonist pitolisant reverses some subchronic disturbances induced by olanzapine in mice. Metab Brain Dis. 2016 Oct;31(5):1023-9.|[4]Ligneau X, et al. BF2.649 [1-{3-[3-(4-Chlorophenyl)propoxy]propyl}piperidine, hydrochloride], a nonimidazole inverse agonist/antagonist at the human histamine H3 receptor: Preclinical pharmacology. J Pharmacol Exp Ther. 2007 Jan;320(1):365-75.
  • Shipping Conditions: Room temperature
  • Clinical Information: No Development Reported