PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
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.	bambuterol	368-378	acetylcholinesterase (Cartwright blood group)	Homo sapiens	91-95	
2906603-5	1988	Because butyrylthiocholine is the preferred substrate for cholinesterase (EC 3.1.1.8) and acetylthiocholine for acetylcholinesterase (EC 3.1.1.7), these results indicate that bambuterol is a remarkably selective and potent inhibitor of cholinesterase.	bambuterol	175-185	acetylcholinesterase (Cartwright blood group)	Homo sapiens	112-132	
18582854-2	2008	In order to relate bambuterol selectivity and stereoselectivity of BChE and acetylcholinesterase (AChE, EC 3.1.1.7) of different species, we studied the inhibition of human, mouse, and horse BChE, as well as AChE of human and mouse by (R)- and (S)-bambuterol.	bambuterol	19-29	acetylcholinesterase (Cartwright blood group)	Homo sapiens	98-102	
18582854-3	2008	AChE and BChE of all studied species were progressively inhibited by both bambuterol enantiomers, with a preference for the (R)-bambuterol whose inhibition rate constants were about five times higher than that of (S)-bambuterol.	bambuterol	213-227	acetylcholinesterase (Cartwright blood group)	Homo sapiens	0-4