PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 35124201-5 2022 6-Benzylaminopurines showed comparable CDK2 inhibitory activity to 6-anilinopurines, however, the PDGFRalpha and FLT3-ITD inhibition was strongly suppressed. benzylaminopurine 0-20 cyclin dependent kinase 2 Homo sapiens 39-43 16386795-1 2006 The synthesis, characterization and biological activity of the first zinc(II) complexes with potent inhibitors of cyclin-dependent kinases (CDKs) derived from 6-benzylaminopurine are described. benzylaminopurine 159-178 cyclin dependent kinase 2 Homo sapiens 140-144 29101605-5 2018 At the same time, insulin and BaP also stimulated the expression of cell cycle proteins viz., Cyclin E and Cdk2, and thus induced more incorporation of Bromodeoxyuridine (BrdU) in cultured cells indicating increased DNA synthesis. benzylaminopurine 30-33 cyclin dependent kinase 2 Homo sapiens 107-111