PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
229216-7	1979	frequency but ambenonium, with a high specificity for acetylcholinesterase, was markedly less effective in this respect.	Ambenonium Chloride	14-24	acetylcholinesterase (Cartwright blood group)	Homo sapiens	54-74	
1588924-0	1992	Ambenonium is a rapidly reversible noncovalent inhibitor of acetylcholinesterase, with one of the highest known affinities.	Ambenonium Chloride	0-10	acetylcholinesterase (Cartwright blood group)	Homo sapiens	60-80	
1926583-2	1991	Such reversible inhibitors as tacrine (of non-competition action), ambenonium (mixed action) and galanthamine (competitive type of action) decelerate the decarbamylation rate of acetylcholinesterase.	Ambenonium Chloride	67-77	acetylcholinesterase (Cartwright blood group)	Homo sapiens	178-198	
15982786-1	2006	Using the in vivo enzyme protection-enzyme inhibition method, we visualized the distribution of the intraventricularly and cisternally (cisterna magna) injected ambenonium chloride (Am) bound reversibly to the extracellular acetylcholinesterase enzyme (AChE) in the rabbit brain in order to describe the extracellular flow pathways from the cerebrospinal fluid (CSF).	Ambenonium Chloride	161-180	acetylcholinesterase (Cartwright blood group)	Homo sapiens	253-257	
13679187-0	2003	Design, synthesis and biological evaluation of ambenonium derivatives as AChE inhibitors.	Ambenonium Chloride	47-57	acetylcholinesterase (Cartwright blood group)	Homo sapiens	73-77	
5833399-0	1965	Affinity of benzoquinonium and ambenonium derivatives for the acetylcholine receptor, tested on the electroplax, and for acetylcholinesterase in solution.	Ambenonium Chloride	31-41	acetylcholinesterase (Cartwright blood group)	Homo sapiens	121-141