PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27088891-6	2016	Among them, luteolin (2), eriodictyol (5), ethyl rosmarinate (13), and clinopodic acids B (14) were proved to be potent alpha-glucosidase inhibitors with IC50 value ranging from 0.6 to 2.0 mum.	Luteolin	12-20	sucrase-isomaltase	Homo sapiens	120-137	
35215317-0	2022	Magnolol and Luteolin Inhibition of alpha-Glucosidase Activity: Kinetics and Type of Interaction Detected by In Vitro and In Silico Studies.	Luteolin	13-21	sucrase-isomaltase	Homo sapiens	36-53	
35215317-2	2022	This research aimed to determine the inhibitory activity of magnolol and luteolin on alpha-glucosidase activity.	Luteolin	73-81	sucrase-isomaltase	Homo sapiens	85-102	
28875706-2	2017	The IC50 values for baicalein, (+)-catechin, quercetin, and luteolin were 74.1 +- 5.6, 175.1 +- 9.1, 281.2 +- 19.2, and 339.4 +- 16.3 muM, respectively, against alpha-glucosidase.	Luteolin	60-68	sucrase-isomaltase	Homo sapiens	161-178	
34641514-3	2021	The alpha-glucosidase inhibitory assay screening resulted in the isolation of eight known compounds of quercetin, quercitrin, luteolin, 5-deoxyluteolin, 4-methyl ether isoliquiritigenin, 3,2",4"-trihydroxy-4-methoxychalcone, stigmasterol and beta-sitosterol.	Luteolin	126-134	sucrase-isomaltase	Homo sapiens	4-21