PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26032855-3	2015	We designed the target compounds as dual binding site acetylcholinesterase inhibitors, where the N-benzylamine pharmacophore is responsible for interactions with the catalytic anionic site of the enzyme.	benzylamine	97-110	acetylcholinesterase (Cartwright blood group)	Homo sapiens	54-74	
25707322-4	2015	We designed the target compounds as dual binding site acetylcholinesterase inhibitors with N-benzylamine moiety interacting with the catalytic site of the enzyme and an isoindoline-1,3-dione fragment interacting with the peripheral anionic site of the enzyme.	benzylamine	91-104	acetylcholinesterase (Cartwright blood group)	Homo sapiens	54-74