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Bioorg Med Chem Lett ; 30(6): 126966, 2020 03 15.
Article in English | MEDLINE | ID: mdl-32001136

ABSTRACT

Herein, we report the discovery of a series of thieno[2,3-d]pyrimidin-4(3H)-one derivatives as a new class of ROCK inhibitors. Structure-activity relationship studies of these compounds led to the identification of the most potent compound, 3-(3-methoxybenzyl)-6-(1H-pyrrolo[2,3-b]pyridin-4-yl)thieno[2,3-d]pyrimidin-4(3H)-one (8k), which showed IC50 values of 0.004 µM and 0.001 µM against ROCK Ⅰ and ROCK Ⅱ, respectively. In vitro, 8k significantly reduced the phosphorylation level of ROCK downstream signaling protein and induce changes in cell morphology and migration. Overall, this study provides a promising lead compound for drug discovery targeting ROCKs.


Subject(s)
Protein Kinase Inhibitors/chemistry , Pyrimidinones/chemistry , rho-Associated Kinases/antagonists & inhibitors , Cell Movement/drug effects , Drug Discovery , Humans , Phosphorylation , Protein Kinase Inhibitors/metabolism , Pyrimidinones/metabolism , Structure-Activity Relationship
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