PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
32887168-3	2020	Specifically, according to the subtle differences structural features and substrate preference between BChE and its sister enzyme AChE, CyClCP was constructed by introducing chlorine atom at the ortho-position of the phenolic hydroxyl in the previous reported probe (CyCP).	Chlorine	174-182	butyrylcholinesterase	Homo sapiens	103-107	
15092450-1	1989	A cheap and simple but very sensitive and specific detection tube has been developed for the detection of cholinesterase-inhibiting compounds in natural and waste water disinfected with chlorine-containing oxidants.	Chlorine	186-194	butyrylcholinesterase	Homo sapiens	106-120	
23679855-6	2013	There is no pocket in hBChE that is able to accommodate the chlorine substituent.	Chlorine	60-68	butyrylcholinesterase	Homo sapiens	22-27	
30680760-6	2019	Most of the compounds that contain para-substituted fluorine or chlorine exhibit potent activity against AChE and poor activity against BChE, while ortho-substituted analogs show the opposite effect.	Chlorine	64-72	butyrylcholinesterase	Homo sapiens	136-140	
30680760-0	2019	Structure-activity study of fluorine or chlorine-substituted cinnamic acid derivatives with tertiary amine side chain in acetylcholinesterase and butyrylcholinesterase inhibition.	Chlorine	40-48	butyrylcholinesterase	Homo sapiens	146-167	
18202915-4	2008	The water samples were treated with chlorine to enhance the ChE-inhibiting activity by conversion of thiophosphate pesticides to phosphate pesticides.	Chlorine	36-44	butyrylcholinesterase	Homo sapiens	60-63	
18202915-5	2008	The ChE-inhibiting activity increased in almost all the chlorine-treated samples, although organophosphorus pesticides were either not detected or detected in traces in the samples by gas chromatographic-mass spectrometric analysis.	Chlorine	56-64	butyrylcholinesterase	Homo sapiens	4-7	
22467030-2	2012	Chlorine was tested as an oxidizing reagent for conversion of various thiophosphorus pesticides (P=S compounds) into their P=O analogs, which have higher ChE-inhibiting activity.	Chlorine	0-8	butyrylcholinesterase	Homo sapiens	154-157	
22467030-4	2012	Greater ChE-inhibiting activities, leading to lower detection limits (ppb levels), were observed for the chlorine-treated solutions fortified azinphos methyl, diazinon, isoxathion and ronnel etc.	Chlorine	105-113	butyrylcholinesterase	Homo sapiens	8-11