PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31255972-3	2019	Based on our previous studies, four pyrimidine-fused heterocycles (PFH) were selected as they revealed satisfactory inhibitory action against mammalian alpha-glucosidase.	pyrimidine	36-46	sucrase-isomaltase	Homo sapiens	152-169	
23978663-0	2013	Synthesis of new pyrimidine-fused derivatives as potent and selective antidiabetic alpha-glucosidase inhibitors.	pyrimidine	17-27	sucrase-isomaltase	Homo sapiens	83-100	
23978663-1	2013	The synthesis of a set of pyrimidine-fused derivatives (L1-L8), resulting from the incorporation of different fragments on the pyrimidine-fused heterocycle (PFH) of the earlier reported alpha-glucosidase (alpha-Gls) inhibitor (C1-C5), allowed the discovery of new ligands with modest and selective inhibitory activity.	pyrimidine	26-36	sucrase-isomaltase	Homo sapiens	186-203	
23978663-1	2013	The synthesis of a set of pyrimidine-fused derivatives (L1-L8), resulting from the incorporation of different fragments on the pyrimidine-fused heterocycle (PFH) of the earlier reported alpha-glucosidase (alpha-Gls) inhibitor (C1-C5), allowed the discovery of new ligands with modest and selective inhibitory activity.	pyrimidine	26-36	sucrase-isomaltase	Homo sapiens	205-214	
24028850-3	2013	Recently, pyrimidine fused heterocycles (PFHs) revealed inhibitory properties against alpha-glucosidase (alpha-Gls) which is an important target enzyme for those drugs playing significant role in treatment of type-II diabetes and HIV/AIDS infection.	pyrimidine	10-20	sucrase-isomaltase	Homo sapiens	86-103	
24028850-3	2013	Recently, pyrimidine fused heterocycles (PFHs) revealed inhibitory properties against alpha-glucosidase (alpha-Gls) which is an important target enzyme for those drugs playing significant role in treatment of type-II diabetes and HIV/AIDS infection.	pyrimidine	10-20	sucrase-isomaltase	Homo sapiens	105-114