cis-4-(Piperazin-1-yl)-5,6,7a,8,9,10,11,11a-octahydrobenzofuro[2,3-h]quinazolin-2-amine (A-987306), A New Histamine H4R Antagonist that Blocks Pain Responses against Carrageenan-Induced Hyperalgesia

Journal of Medicinal Chemistry
2008.0

Abstract

cis-4-(Piperazin-1-yl)-5,6,7a,8,9,10,11,11a-octahydrobenzofuro[2,3-h]quinazolin-2-amine, 4 (A-987306) is a new histamine H(4) antagonist. The compound is potent in H(4) receptor binding assays (rat H(4), K(i) = 3.4 nM, human H(4) K(i) = 5.8 nM) and demonstrated potent functional antagonism in vitro at human, rat, and mouse H(4) receptors in cell-based FLIPR assays. Compound 4 also demonstrated H(4) antagonism in vivo in mice, blocking H(4)-agonist induced scratch responses, and showed anti-inflammatory activity in mice in a peritonitis model. Most interesting was the high potency and efficacy of this compound in blocking pain responses, where it showed an ED(50) of 42 mumol/kg (ip) in a rat post-carrageenan thermal hyperalgesia model of inflammatory pain.

Knowledge Graph

Similar Paper

cis-4-(Piperazin-1-yl)-5,6,7a,8,9,10,11,11a-octahydrobenzofuro[2,3-h]quinazolin-2-amine (A-987306), A New Histamine H<sub>4</sub>R Antagonist that Blocks Pain Responses against Carrageenan-Induced Hyperalgesia
Journal of Medicinal Chemistry 2008.0
Rotationally Constrained 2,4-Diamino-5,6-disubstituted Pyrimidines: A New Class of Histamine H<sub>4</sub>Receptor Antagonists with Improved Druglikeness and in Vivo Efficacy in Pain and Inflammation Models
Journal of Medicinal Chemistry 2008.0
Fragment Based Design of New H<sub>4</sub>Receptor−Ligands with Anti-inflammatory Properties in Vivo
Journal of Medicinal Chemistry 2008.0
Alkyl derivatives of 1,3,5-triazine as histamine H4 receptor ligands
Bioorganic &amp; Medicinal Chemistry 2019.0
Ligand based design of novel histamine H4 receptor antagonists; fragment optimization and analysis of binding kinetics
Bioorganic &amp; Medicinal Chemistry Letters 2012.0
Aryl-1,3,5-triazine derivatives as histamine H4 receptor ligands
European Journal of Medicinal Chemistry 2014.0
Discovery of Quinazolines as Histamine H<sub>4</sub>Receptor Inverse Agonists Using a Scaffold Hopping Approach
Journal of Medicinal Chemistry 2008.0
(2-Arylethenyl)-1,3,5-triazin-2-amines as a novel histamine H4 receptor ligands
European Journal of Medicinal Chemistry 2015.0
Synthesis and QSAR of Quinazoline Sulfonamides As Highly Potent Human Histamine H<sub>4</sub> Receptor Inverse Agonists
Journal of Medicinal Chemistry 2010.0
Synthesis and structure–activity relationships of indole and benzimidazole piperazines as histamine H4 receptor antagonists
Bioorganic &amp; Medicinal Chemistry Letters 2004.0