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Bioorg Med Chem ; 41: 116216, 2021 07 01.
Article in English | MEDLINE | ID: mdl-34023664

ABSTRACT

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.


Subject(s)
Cyclohexylamines/pharmacology , Epoxide Hydrolases/antagonists & inhibitors , Triazines/pharmacology , Cyclohexylamines/chemistry , Drug Discovery , Humans , Molecular Structure , Pulmonary Disease, Chronic Obstructive/drug therapy , Small Molecule Libraries , Triazines/chemistry
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