PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27940419-0	2017	Novel CLK1 inhibitors based on N-aryloxazol-2-amine skeleton - A possible way to dual VEGFR2 TK/CLK ligands.	n-aryloxazol-2-amine	31-51	kinase insert domain receptor	Homo sapiens	86-92	
27940419-8	2017	We proposed that our inhibitors have similar binding places and interactions in CLK1, 3 and VEGFR2 TK mostly due to the joint N-aryloxazol-2-amine pharmacophoric fragment.	n-aryloxazol-2-amine	126-146	kinase insert domain receptor	Homo sapiens	92-98