PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
17266627-0	2007	3D-QSAR CoMFA study on oxindole derivatives as cyclin dependent kinase 1 (CDK1) and cyclin dependent kinase 2 (CDK2) inhibitors.	2-oxindole	23-31	cyclin dependent kinase 2	Homo sapiens	84-109	
17266627-0	2007	3D-QSAR CoMFA study on oxindole derivatives as cyclin dependent kinase 1 (CDK1) and cyclin dependent kinase 2 (CDK2) inhibitors.	2-oxindole	23-31	cyclin dependent kinase 2	Homo sapiens	111-115	
17266627-2	2007	With the purpose of designing new chemical entities with enhanced inhibitory potencies against cyclin dependent kinase 2 (CDK2) and cyclin dependent kinase 1 (CDK1), the 3D-QSAR CoMFA study carried out on oxindole derivatives as inhibitors of these kinases is presented here.	2-oxindole	205-213	cyclin dependent kinase 2	Homo sapiens	95-120	
17266627-2	2007	With the purpose of designing new chemical entities with enhanced inhibitory potencies against cyclin dependent kinase 2 (CDK2) and cyclin dependent kinase 1 (CDK1), the 3D-QSAR CoMFA study carried out on oxindole derivatives as inhibitors of these kinases is presented here.	2-oxindole	205-213	cyclin dependent kinase 2	Homo sapiens	122-126