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Bioorg Med Chem ; 41: 116216, 2021 07 01.
Artigo em Inglês | MEDLINE | ID: mdl-34023664

RESUMO

Inhibition of soluble epoxide hydrolase (sEH) has recently emerged as a new approach to treat cardiovascular disease and respiratory disease. Inhibitors based on 1,3,5-triazine chemotype were discovered through affinity selection against two triazine-based DNA-encoded libraries. The structure and activity relationship study led to the expansion of the original 1,4-cycloalkyl series to related aniline, piperidine, quinoline, aryl-ether and benzylic series. The 1,3-cycloalkyl chemotype led to the discovery of a clinical candidate (GSK2256294) for COPD.


Assuntos
Cicloexilaminas/farmacologia , Epóxido Hidrolases/antagonistas & inibidores , Triazinas/farmacologia , Cicloexilaminas/química , Descoberta de Drogas , Humanos , Estrutura Molecular , Doença Pulmonar Obstrutiva Crônica/tratamento farmacológico , Bibliotecas de Moléculas Pequenas , Triazinas/química
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