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	
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	
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