PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
3468911-2	1986	When the maximal effects of these solvents were tested at +37 degrees C, they diminished the AchE activity: benzene 75%, xylene 65%, styrene 80%, trichloroethylene 55%, tetrachloroethylene 60%, 1,1,1-trichloroethane 25%, and 1,1,2,2-tetrachloroethane 75%.	Benzene	108-115	acetylcholinesterase (Cartwright blood group)	Homo sapiens	93-97	
17994573-4	2007	Therefore, benzene-1,4-di-N-substituted carbamates (para compounds), with the angle of 180 degrees between two C(benzene)-O bonds, mimic the preferable anti C-O/C-N conformers of acetylcholine for the choline ethylene backbone in the acetylcholinesterase catalysis.	Benzene	11-18	acetylcholinesterase (Cartwright blood group)	Homo sapiens	234-254	
30934674-0	2019	Novel Benzene-Based Carbamates for AChE/BChE Inhibition: Synthesis and Ligand/Structure-Oriented SAR Study.	Benzene	6-13	acetylcholinesterase (Cartwright blood group)	Homo sapiens	35-39	
29447012-4	2018	Unsaturated bond and benzene ring in cinnamic acid scaffold seems important for the inhibitory activity against AChE.	Benzene	21-28	acetylcholinesterase (Cartwright blood group)	Homo sapiens	112-116	
25462245-1	2015	A new series of tacrine-based acetylcholinesterase (AChE) inhibitors 7a-l were designed by replacing the benzene ring of tacrine with aryl-dihydropyrano[2,3-c]pyrazole.	Benzene	105-112	acetylcholinesterase (Cartwright blood group)	Homo sapiens	52-56	
22972560-1	2012	A quantitative analysis of the interaction sites of the anti-Alzheimer drug galanthamine with molecular probes (water and benzene molecules) representative of its surroundings in the binding site of acetylcholinesterase (AChE) has been realized through pairwise potentials calculations and quantum chemistry.	Benzene	122-129	acetylcholinesterase (Cartwright blood group)	Homo sapiens	199-219	
22972560-1	2012	A quantitative analysis of the interaction sites of the anti-Alzheimer drug galanthamine with molecular probes (water and benzene molecules) representative of its surroundings in the binding site of acetylcholinesterase (AChE) has been realized through pairwise potentials calculations and quantum chemistry.	Benzene	122-129	acetylcholinesterase (Cartwright blood group)	Homo sapiens	221-225	
22425563-2	2012	Simple indoles with substitution of methoxy, carboxy or hydroxy at the benzene ring showed a low percent of inhibitory activity in eel-AChE.	Benzene	71-78	acetylcholinesterase (Cartwright blood group)	Homo sapiens	135-139