| Literature DB >> 27423478 |
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.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