PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20487840-1	1981	Esters of dimethylcarbamic acid are known to be poor substrates of acetylcholinesterase.	N,N-dimethylcarbamate	10-31	acetylcholinesterase (Cartwright blood group)	Homo sapiens	67-87	
26869193-1	2016	We have previously shown the improved acetylcholinesterase inhibitory activity of a model hydroxypyridinone compound transforming the hydroxyl group on the main ring into an N,N-dimethylcarbamate group; in the course of that study we developed a computational model to screen compounds for enzymatic activity.	N,N-dimethylcarbamate	174-195	acetylcholinesterase (Cartwright blood group)	Homo sapiens	38-58	
27594053-0	2016	New N,N-dimethylcarbamate inhibitors of acetylcholinesterase: design synthesis and biological evaluation.	N,N-dimethylcarbamate	4-25	acetylcholinesterase (Cartwright blood group)	Homo sapiens	40-60	
27594053-1	2016	A series of N,N-dimethylcarbamates containing a N,N-dibenzylamino moiety was synthesized and tested to evaluate their ability to inhibit Acetylcholinesterase (AChE).	N,N-dimethylcarbamate	12-34	acetylcholinesterase (Cartwright blood group)	Homo sapiens	137-157	
27594053-1	2016	A series of N,N-dimethylcarbamates containing a N,N-dibenzylamino moiety was synthesized and tested to evaluate their ability to inhibit Acetylcholinesterase (AChE).	N,N-dimethylcarbamate	12-34	acetylcholinesterase (Cartwright blood group)	Homo sapiens	159-163