Design, synthesis and biological evaluation of novel pyrimido[4,5-d]pyrimidine CDK2 inhibitors as anti-tumor agents

Abstract

A series of 2,5,7-trisubstituted pyrimido[4,5-d]pyrimidine cyclin-dependent kinase (CDK2) inhibitors is designed and synthesized. 6-Amino-2-thiouracil is reacted with an aldehyde and thiourea to prepare the pyrimido[4,5-d]-pyrimidines. Alkylation and amination of the latter ones give different amino derivatives. These compounds show potent and selective CDK inhibitory activities and inhibit in vitro cellular proliferation in cultured human tumor cells. © El-Moghazy et al.; licensee Österreichische Apotheker-Verlagsgesellschaft m. b. H., Vienna, Austria.