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Basic Information

ID: ALA3400068

Journal: Bioorg Med Chem

Title: Novel arylazopyrazole inhibitors of cyclin-dependent kinases.

Authors: Jorda R, Schütznerová E, Cankař P, Brychtová V, Navrátilová J, Kryštof V.

Abstract: Here, we describe new 4-arylazo-3,5-diamino-1H-pyrazole derivatives developed from CAN508, one of the first inhibitors to show preference for transcriptional regulator cyclin-dependent kinase 9. By substituting nitrogen in the pyrazole ring and employing a heteroatom in the 4-aryl ring, we obtained more potent derivatives differing in their CDK-selectivity profiles. The antiproliferative and anti-CDK kinase activities of the novel arylazopyrazoles were examined. The cellular effect of compound IVc was studied on MCF-7 cells synchronized by various methods and compared with other selective CDK inhibitors. The results demonstrated that IVc shows a preference for CDK4 and CDK1. In contrast to cytostatic effects induced by IVc in MCF-7 and K562 cells, we observed apoptotic activities in the RPMI-8226 cell line, which were confirmed by detecting active caspases by different biochemical assays.

CiteXplore: 25835357

DOI: 10.1016/j.bmc.2015.03.025