PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
32736114-3	2020	For phenotypic analysis of CES1 and CES2 activity, we used the hydrolysis metabolism of 2-(2-benzoyl3-methoxyphenyl) benzothiazole (BMBT) and fluorescein diacetate (FD) catalyzed by human liver microsomes (HLMs) as the probe reactions.	diacetylfluorescein	142-163	carboxylesterase 2	Homo sapiens	36-40	
26164127-7	2015	Recombinant AADAC catalyzed the hydrolysis of fluorescein diacetate, N-monoacetyldapsone, and propanil, which possess notably small acyl moieties, and these substrates were also hydrolyzed by CES2.	diacetylfluorescein	46-67	carboxylesterase 2	Homo sapiens	192-196	
30486721-6	2019	In vitro human liver microsomes (HLMs)-catalyzed hydrolysis of 2-(2-Benzoyl-3-methoxyphenyl) benzothiazole (BMBT) and fluorescein diacetate (FD) was employed as the probe reaction for CES1 and CES2, respectively.	diacetylfluorescein	118-139	carboxylesterase 2	Homo sapiens	193-197	
29468758-3	2018	In this study, the inhibitory effects of shikonin on the activity of hCE2 in human liver microsomes are investigated by using fluorescein diacetate (FD), N-(2-butyl-1,3-dioxo-2,3-dihydro-1H-phenalen-6-yl)-2-chloroacetamide (NCEN), and CPT-11 as substrates of hCE2.	diacetylfluorescein	126-147	carboxylesterase 2	Homo sapiens	69-73	
21540359-0	2011	Characterization of recombinant human carboxylesterases: fluorescein diacetate as a probe substrate for human carboxylesterase 2.	diacetylfluorescein	57-78	carboxylesterase 2	Homo sapiens	110-128