Bavisant dihydrochloride hydrate


CAS No. : 1103522-80-0

Bavisant dihydrochloride hydrate,1103522-80-0
Product Details
For research use only. Not Intended for Therapeutic Use!
Cat No:I000426
Synonyms:(4-cyclopropylpiperazin-1-yl)-[4-(morpholin-4-ylmethyl)phenyl]methanone;hydrate;dihydrochloride
Molecular Formula:C19H31Cl2N3O3
Molecular Weight:420.37
Target:Histamine Receptor
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Cat No:I000426
Cas No:1103522-80-0
Product-Name:Bavisant dihydrochloride hydrate

Bavisant Hcl hydrate(JNJ-31001074) is a highly selective, orally active antagonist of the human H3 receptor with a novel mechanism of action, involving wakefulness and cognition, with potential as a treatment for ADHD.
IC50 Value:
Target: H3 receptor
in vitro: Bavisant completed a phase II ADHD trial, but no results have been reported [1].
in vivo: Mean change from baseline in the total ADHD-RS-IV score at day 42 (primary efficacy endpoint) was -8.8 in the placebo group versus -9.3, -11.2 and -12.2 in the bavisant 1mg/day, 3mg/day and 10mg/day groups, respectively; the change in the 10mg/day group was not statistically superior to placebo (p=0.161), and hence statistical comparisons of the 1mg/day and 3mg/day groups with placebo based on a step-down closed testing procedure were not performed [2].
Clinical trial: A Study to Characterize the Pharmacokinetics and Effect of Food on JNJ-31001074 in Healthy Volunteers. Phase 2


[1]. Robert L. Hudkins, Rita Raddatz, Ming Tao, Discovery and Characterization of 6-{4-[3-(R)-2-Methylpyrrolidin-1-yl)propoxy]phenyl}-2H-pyridazin-3-one (CEP-26401, Irdabisant): A Potent, Selective Histamine H3 Receptor Inverse Agonist. J. Med. Chem. 2011, 54, 4781-4792
[2]. Weisler RH, Pandina GJ, Daly EJ, Randomized clinical study of a histamine H3 receptor antagonist for the treatment of adults with attention-deficit hyperactivity disorder. CNS Drugs. 2012 May 1;26(5):421-34.

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