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Bavisant Sale

(Synonyms: JNJ-31001074) 目录号 : GC35471

Bavisant (JNJ-31001074)是口服活性人H3受体拮抗剂。

Bavisant Chemical Structure

Cas No.:929622-08-2

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2mg
¥1,294.00
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5mg
¥1,890.00
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10mg
¥2,970.00
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50mg
¥7,533.00
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100mg
¥11,718.00
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Sample solution is provided at 25 µL, 10mM.

Description

Bavisant (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 receptorin 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 1•mg/day, 3•mg/day and 10•mg/day groups, respectively; the change in the 10•mg/day group was not statistically superior to placebo (p=0.161), and hence statistical comparisons of the 1•mg/day and 3•mg/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, et al. 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.

化学性质

Cas No. 929622-08-2 SDF
别名 JNJ-31001074
Canonical SMILES O=C(N1CCN(C2CC2)CC1)C(C=C3)=CC=C3CN4CCOCC4
分子式 C19H27N3O2 分子量 329.44
溶解度 DMSO : 100 mg/mL (303.55 mM; Need ultrasonic) 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 3.0355 mL 15.1773 mL 30.3545 mL
5 mM 0.6071 mL 3.0355 mL 6.0709 mL
10 mM 0.3035 mL 1.5177 mL 3.0355 mL
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