PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16140252-13	2005	Using the kinase inhibitors BMS-250595, purvalanol B, AG-12275, flavopiridol, and several other compounds, it is demonstrated that one can obtain excellent comparisons between the Kd values of binding to CDK2 obtained by TdCD and ITC.	purvalanol B	40-52	cyclin dependent kinase 2	Homo sapiens	204-208	
16733081-5	2006	This effect on RGS2 mRNA was blocked by the cyclin-dependent kinase-2 (cdk2) inhibitors roscovitine and purvalanol.	purvalanol B	104-114	cyclin dependent kinase 2	Homo sapiens	44-69	
16733081-5	2006	This effect on RGS2 mRNA was blocked by the cyclin-dependent kinase-2 (cdk2) inhibitors roscovitine and purvalanol.	purvalanol B	104-114	cyclin dependent kinase 2	Homo sapiens	71-75	
33048473-11	2020	Pharmacological analysis showed that the administration of two cell cycle inhibitors for inactivating CDC25A phosphatase (NSC95397) and the cyclin E2/cyclin-dependent kinase 2 (CDK2) complex (purvalanol A) increased the dome number independently of MTA.	purvalanol B	192-202	cyclin dependent kinase 2	Homo sapiens	177-181