PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
22867529-5	2013	The docking results also showed that the formation of new H-bonds between the N-H of the ethylenediamine group linked to the 6-alkoxy site and Asp776/Cys773 in the binding pocket of EGFR makes compounds 19 (IC50=12.1+-1.6 nM) and 20 (IC50=13.6+-0.8 nM) the most potent EGFR inhibitors in this class and worthy of further modification to obtain more potent anticancer compounds.	ethylenediamine	89-104	epidermal growth factor receptor	Homo sapiens	182-186	
22867529-5	2013	The docking results also showed that the formation of new H-bonds between the N-H of the ethylenediamine group linked to the 6-alkoxy site and Asp776/Cys773 in the binding pocket of EGFR makes compounds 19 (IC50=12.1+-1.6 nM) and 20 (IC50=13.6+-0.8 nM) the most potent EGFR inhibitors in this class and worthy of further modification to obtain more potent anticancer compounds.	ethylenediamine	89-104	epidermal growth factor receptor	Homo sapiens	269-273