PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 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 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 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 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