PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31675511-0	2020	6-Methyluracil derivatives as peripheral site ligand-hydroxamic acid conjugates: Reactivation for paraoxon-inhibited acetylcholinesterase.	6-methyluracil	0-14	acetylcholinesterase (Cartwright blood group)	Homo sapiens	117-137	
17929660-0	2007	Effect of a tetraalkylammonium derivative of 6-methyluracil from a new class of acetylcholinesterase inhibitors on the endplate potential amplitude in muscles of different function types under high-frequency nerve stimulation.	6-methyluracil	45-59	acetylcholinesterase (Cartwright blood group)	Homo sapiens	80-100	
31675511-2	2020	Using paraoxon (POX) as a model organophosphate, it was shown that 6-methyluracil derivatives linked with hydroxamic acid are able to reactivate POX-inhibited human acetylcholinesterase (AChE) in vitro.	6-methyluracil	67-81	acetylcholinesterase (Cartwright blood group)	Homo sapiens	165-185	
31675511-2	2020	Using paraoxon (POX) as a model organophosphate, it was shown that 6-methyluracil derivatives linked with hydroxamic acid are able to reactivate POX-inhibited human acetylcholinesterase (AChE) in vitro.	6-methyluracil	67-81	acetylcholinesterase (Cartwright blood group)	Homo sapiens	187-191	
26639720-14	2015	In the present study, taking acyclic derivatives of 6-methyluracil as a model AChE inhibitor, we attempted to develop AChE inhibitors that specifically bind to the PAS with weak binding to the active site of AChE.	6-methyluracil	52-66	acetylcholinesterase (Cartwright blood group)	Homo sapiens	78-82	
26639720-0	2015	Macrocyclic derivatives of 6-methyluracil: New ligands of the peripheral anionic site of acetylcholinesterase.	6-methyluracil	27-41	acetylcholinesterase (Cartwright blood group)	Homo sapiens	89-109	
26639720-13	2015	RESULTS: We described previously a new class of selective mammalian AChE vs. butyrylcholinesterase (BChE) inhibitors based on alkylammonium derivatives of 6-methyluracil of acyclic topology [7].	6-methyluracil	155-169	acetylcholinesterase (Cartwright blood group)	Homo sapiens	68-72	
26929400-0	2016	Slow-binding inhibition of acetylcholinesterase by an alkylammonium derivative of 6-methyluracil: mechanism and possible advantages for myasthenia gravis treatment.	6-methyluracil	82-96	acetylcholinesterase (Cartwright blood group)	Homo sapiens	27-47	
26929400-1	2016	Inhibition of human AChE (acetylcholinesterase) and BChE (butyrylcholinesterase) by an alkylammonium derivative of 6-methyluracil, C-547, a potential drug for the treatment of MG (myasthenia gravis) was studied.	6-methyluracil	115-129	acetylcholinesterase (Cartwright blood group)	Homo sapiens	20-24	
26929400-1	2016	Inhibition of human AChE (acetylcholinesterase) and BChE (butyrylcholinesterase) by an alkylammonium derivative of 6-methyluracil, C-547, a potential drug for the treatment of MG (myasthenia gravis) was studied.	6-methyluracil	115-129	acetylcholinesterase (Cartwright blood group)	Homo sapiens	26-46	
26639720-14	2015	In the present study, taking acyclic derivatives of 6-methyluracil as a model AChE inhibitor, we attempted to develop AChE inhibitors that specifically bind to the PAS with weak binding to the active site of AChE.	6-methyluracil	52-66	acetylcholinesterase (Cartwright blood group)	Homo sapiens	118-122	
26639720-14	2015	In the present study, taking acyclic derivatives of 6-methyluracil as a model AChE inhibitor, we attempted to develop AChE inhibitors that specifically bind to the PAS with weak binding to the active site of AChE.	6-methyluracil	52-66	acetylcholinesterase (Cartwright blood group)	Homo sapiens	118-122