PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
35442162-3	2022	In addition, enzyme inhibitory properties of the newly synthesized Schiff bases were determined against acetylcholinesterase (AChE).	Schiff Bases	67-79	acetylcholinesterase (Cartwright blood group)	Homo sapiens	104-124	
34743300-10	2021	The Schiff base ligand was discovered to be the best inhibitor for the AChE and BChE with the values of 7.13 +- 0.84 microM and 5.75 +- 1.03 microM Ki, respectively.	Schiff Bases	4-15	acetylcholinesterase (Cartwright blood group)	Homo sapiens	71-75	
34743300-13	2021	The metal complexes demonstrated better binding affinities with the AChE, BChE, and GST enzymes than the Schiff base ligand.	Schiff Bases	105-116	acetylcholinesterase (Cartwright blood group)	Homo sapiens	68-72	
34743300-14	2021	This study identified a potential Schiff base molecule against both AChE and BChE targets to further investigate for in vivo and safety evaluation.	Schiff Bases	34-45	acetylcholinesterase (Cartwright blood group)	Homo sapiens	68-72	
35442162-3	2022	In addition, enzyme inhibitory properties of the newly synthesized Schiff bases were determined against acetylcholinesterase (AChE).	Schiff Bases	67-79	acetylcholinesterase (Cartwright blood group)	Homo sapiens	126-130	
31193469-0	2019	Synthesis, crystal structures, Hirshfeld surface analysis and spectroscopic studies of two Schiff bases of anisaldehyde and their urease and acetylcholinesterase inhibitory and antioxidant properties.	Schiff Bases	91-103	acetylcholinesterase (Cartwright blood group)	Homo sapiens	141-161	
22391555-2	2013	The AChE-ICERs were prepared by using the homobifunctional linker glutaraldehyde through Schiff base linkage.	Schiff Bases	89-100	acetylcholinesterase (Cartwright blood group)	Homo sapiens	4-8	
25462993-1	2014	Novel aromatic embedded Schiff bases have been synthesized in ionic liquid [bmim]Br and evaluated in vitro for their acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes inhibitory activities.	Schiff Bases	24-36	acetylcholinesterase (Cartwright blood group)	Homo sapiens	117-137	
25462993-1	2014	Novel aromatic embedded Schiff bases have been synthesized in ionic liquid [bmim]Br and evaluated in vitro for their acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes inhibitory activities.	Schiff Bases	24-36	acetylcholinesterase (Cartwright blood group)	Homo sapiens	139-143	
30033646-0	2018	Schiff bases and their amines: Synthesis and discovery of carbonic anhydrase and acetylcholinesterase enzymes inhibitors.	Schiff Bases	0-12	acetylcholinesterase (Cartwright blood group)	Homo sapiens	81-101	
27441832-0	2016	Synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory potential of hydrazide based Schiff bases.	Schiff Bases	110-122	acetylcholinesterase (Cartwright blood group)	Homo sapiens	23-43	
22064271-0	2011	Synthesis, characterization, acetylcholinesterase inhibition, molecular modeling and antioxidant activities of some novel Schiff bases derived from 1-(2-ketoiminoethyl)piperazines.	Schiff Bases	122-134	acetylcholinesterase (Cartwright blood group)	Homo sapiens	29-49