Literature DB >> 27423478

New P2X3 receptor antagonists. Part 1: Discovery and optimization of tricyclic compounds.

Gábor Szántó1, Attila Makó1, Imre Bata1, Bence Farkas1, Sándor Kolok1, Mónika Vastag1, Attila Cselenyák1.   

Abstract

Purinergic P2X3 receptors are trimeric ligand-gated ion channels whose antagonism is an appealing yet challenging and not fully validated drug development idea. With the aim of identification of an orally active, potent human P2X3 receptor antagonist compound that can penetrate the central nervous system, the compound collection of Gedeon Richter was screened. A hit series of tricyclic compounds was subjected to a rapid, two-step optimization process focusing on increasing potency, improving metabolic stability and CNS penetrability. Attempts resulted in compound 65, a potential tool compound for testing P2X3 inhibitory effects in vivo.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  ATP; Airway hyperractivity; Chirality; HTS campaign; Ion channel; New binding site; P2X3 antagonist; Purinergic receptor

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Year:  2016        PMID: 27423478     DOI: 10.1016/j.bmcl.2016.07.009

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Druggable negative allosteric site of P2X3 receptors.

Authors:  Jin Wang; Yao Wang; Wen-Wen Cui; Yichen Huang; Yang Yang; Yan Liu; Wen-Shan Zhao; Xiao-Yang Cheng; Wang-Sheng Sun; Peng Cao; Michael X Zhu; Rui Wang; Motoyuki Hattori; Ye Yu
Journal:  Proc Natl Acad Sci U S A       Date:  2018-04-19       Impact factor: 11.205

  1 in total

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