PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23962483-5	2013	It became evident that pralidoxime and obidoxime in therapeutic concentrations aggravate the inhibition of AChE by carbaryl and propoxur, with obidoxime being substantially more potent compared to 2-PAM.	Propoxur	128-136	acetylcholinesterase (Cartwright blood group)	Homo sapiens	107-111	
22817559-4	2012	The aim of our study was to investigate inhibition of human BChE and acetylcholinesterase (AChE) with metaproterenol, isoproterenol, and newly synthesized racemic bisdimethylcarbamate derivatives of metaproterenol (metacarb) and isoproterenol (isocarb) and their (R)-enantiomers to see if their bioconversion is affected by BChE inhibition in the same way as that for bambuterol.	Propoxur	244-251	acetylcholinesterase (Cartwright blood group)	Homo sapiens	91-95	
22817559-5	2012	Metacarb and isocarb proved to be selective BChE inhibitors, as they progressively inhibited AChE 960 to 80 times more slowly than BChE(UU).	Propoxur	13-20	acetylcholinesterase (Cartwright blood group)	Homo sapiens	93-97	
11129708-17	2000	The AChE inhibition coefficient (ki) with propoxur was 1.86+/-0.24 x 10(5) M(-)1 min(-1) for Cx.	Propoxur	42-50	acetylcholinesterase (Cartwright blood group)	Homo sapiens	4-8