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Bioorg Med Chem Lett ; 28(8): 1392-1396, 2018 05 01.
Article in English | MEDLINE | ID: mdl-29548573

ABSTRACT

A second-generation small molecule P2X3 receptor antagonist has been developed. The lead optimization strategy to address shortcomings of the first-generation preclinical lead compound is described herein. These studies were directed towards the identification and amelioration of preclinical hepatobiliary findings, reducing potential for drug-drug interactions, and decreasing the projected human dose of the first-generation lead.


Subject(s)
Analgesics/therapeutic use , Benzamides/therapeutic use , Pain/drug therapy , Purinergic P2X Receptor Antagonists/therapeutic use , Pyridines/therapeutic use , Receptors, Purinergic P2X3/metabolism , Analgesics/chemical synthesis , Analgesics/chemistry , Analgesics/pharmacokinetics , Animals , Benzamides/chemical synthesis , Benzamides/chemistry , Benzamides/pharmacokinetics , Dogs , Drug Design , Drug Interactions , Glucuronosyltransferase/antagonists & inhibitors , Half-Life , Hyperbilirubinemia/prevention & control , Molecular Structure , Purinergic P2X Receptor Antagonists/chemical synthesis , Purinergic P2X Receptor Antagonists/chemistry , Purinergic P2X Receptor Antagonists/pharmacokinetics , Pyridines/chemical synthesis , Pyridines/chemistry , Pyridines/pharmacokinetics , Rats , Stereoisomerism , Structure-Activity Relationship
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