Title : Synthesis of a new series of pyrazolo[1,5-a]pyrimidines as CDK2 inhibitors and anti-leukemia.

Pub. Date : 2021 Dec

PMID : 34688130






2 Functional Relationships(s)
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1 The 7-(4-Bromo-phenyl)-3-(3-chloro/2-chloro-phenylazo)-pyrazolo(1,5-a)pyrimidin-2-ylamines 5 h and 5i revealed the best CDK2 inhibitory activity with comparable potency (IC50 = 22 and 24 nM, respectively) to that of dinaciclib (IC50 = 18 nM). dinaciclib cyclin dependent kinase 2 Homo sapiens
2 The molecular docking simulations indicated, as expected, that the dinaciclib analogues can well-accommodate the CDK2 binding site, forming a variety of interactions. dinaciclib cyclin dependent kinase 2 Homo sapiens