PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26032855-5	2015	Based on the results of the pharmacological evaluation, we identified compound 8b with a saccharine moiety as the most potent and selective human acetylcholinesterase inhibitor (IC50  = 33 nM) and beta amyloid aggregation inhibitor.	Saccharin	89-99	acetylcholinesterase (Cartwright blood group)	Homo sapiens	146-166	
27721153-3	2017	In vitro studies showed that the majority of saccharin derivatives with piperazine moiety and one phthalimide derivative with 3-aminopiperidine fragment exhibited inhibitory potency toward acetylcholinesterase (AChE) with EeAChE IC50 values ranging from 0.83 muM to 19.18 muM.	Saccharin	45-54	acetylcholinesterase (Cartwright blood group)	Homo sapiens	189-209	
27721153-3	2017	In vitro studies showed that the majority of saccharin derivatives with piperazine moiety and one phthalimide derivative with 3-aminopiperidine fragment exhibited inhibitory potency toward acetylcholinesterase (AChE) with EeAChE IC50 values ranging from 0.83 muM to 19.18 muM.	Saccharin	45-54	acetylcholinesterase (Cartwright blood group)	Homo sapiens	211-215