PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
6492073-5	1984	With imidazolium compound in excess over inhibited enzyme, the kinetics of reactivation are well behaved for EPMP-inhibited AChE and depend on the nature of the alkyl ether group R. For GD-inhibited AChE, maximal reactivation was used to compare compounds because rapid phosphonyl enzyme dealkylation and enzyme reinhibition complicate interpretation of kinetic constants.	Ethyl 4-nitrophenyl methylphosphonate	109-113	acetylcholinesterase (Cartwright blood group)	Homo sapiens	124-128	
6492073-5	1984	With imidazolium compound in excess over inhibited enzyme, the kinetics of reactivation are well behaved for EPMP-inhibited AChE and depend on the nature of the alkyl ether group R. For GD-inhibited AChE, maximal reactivation was used to compare compounds because rapid phosphonyl enzyme dealkylation and enzyme reinhibition complicate interpretation of kinetic constants.	Ethyl 4-nitrophenyl methylphosphonate	109-113	acetylcholinesterase (Cartwright blood group)	Homo sapiens	199-203	
2913311-5	1989	The alkynyloxy-substituted compounds were also evaluated in vitro with respect to reversible inhibition of human erythrocyte (RBC) acetylcholinesterase (AChE) and kinetics of reactivation of human AChE inhibited by ethyl p-nitrophenyl methylphosphonate (EPMP).	Ethyl 4-nitrophenyl methylphosphonate	254-258	acetylcholinesterase (Cartwright blood group)	Homo sapiens	197-201