PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23886696-1	2013	Two series of novel acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitors containing benzimidazole core structure were synthesized by a four-step reaction pathway starting from 4-fluoro-3-nitrobenzoic acid as the basic compound.	benzimidazole	103-116	acetylcholinesterase (Cartwright blood group)	Homo sapiens	20-40	
23886696-1	2013	Two series of novel acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitors containing benzimidazole core structure were synthesized by a four-step reaction pathway starting from 4-fluoro-3-nitrobenzoic acid as the basic compound.	benzimidazole	103-116	acetylcholinesterase (Cartwright blood group)	Homo sapiens	42-46	
34931332-0	2022	Design, synthesis, biological activity, molecular docking, and molecular dynamics of novel benzimidazole derivatives as potential AChE/MAO-B dual inhibitors.	benzimidazole	91-104	acetylcholinesterase (Cartwright blood group)	Homo sapiens	130-134	
34931332-1	2022	To develop new acetylcholinesterase (AChE)-monoamine oxidase-B (MAO-B) dual inhibitors against Alzheimer"s disease, the benzimidazole ring, which has a propargyl side chain with previously proven selective MAO-B inhibitory activity, was used as the main structure.	benzimidazole	120-133	acetylcholinesterase (Cartwright blood group)	Homo sapiens	15-35	
34931332-1	2022	To develop new acetylcholinesterase (AChE)-monoamine oxidase-B (MAO-B) dual inhibitors against Alzheimer"s disease, the benzimidazole ring, which has a propargyl side chain with previously proven selective MAO-B inhibitory activity, was used as the main structure.	benzimidazole	120-133	acetylcholinesterase (Cartwright blood group)	Homo sapiens	37-41	
30823470-0	2019	Synthesis and AChE-Inhibitory Activity of New Benzimidazole Derivatives.	benzimidazole	46-59	acetylcholinesterase (Cartwright blood group)	Homo sapiens	14-18	
30823470-5	2019	Among them, compounds 3d and 3h, which featured 3,4-dihydroxy substitution at the phenyl ring and 5(6)-chloro substitution at the benzimidazole ring were found to be potent inhibitors of AChE.	benzimidazole	130-143	acetylcholinesterase (Cartwright blood group)	Homo sapiens	187-191	
23891231-0	2013	Synthesis, biological activity and molecular modeling studies on 1H-benzimidazole derivatives as acetylcholinesterase inhibitors.	benzimidazole	65-81	acetylcholinesterase (Cartwright blood group)	Homo sapiens	97-117	
31135232-0	2021	Investigation of the toxicological and inhibitory effects of some benzimidazole agents on acetylcholinesterase and butyrylcholinesterase enzymes.	benzimidazole	66-79	acetylcholinesterase (Cartwright blood group)	Homo sapiens	90-110