PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8894097-2	1996	The results of this study revealed that (a) inhibitory activity is dependent on the nature and pKa of the leaving group, and (b) the synthesized saccharin derivatives exhibit selective inhibition toward HLE and PR 3, with low or no activity toward cathepsin G.	Saccharin	145-154	proteinase 3	Homo sapiens	211-215	
8806743-0	1996	Amino acid-derived phthalimide and saccharin derivatives as inhibitors of human leukocyte elastase, cathepsin G, and proteinase 3.	Saccharin	35-44	proteinase 3	Homo sapiens	117-129	
7796053-1	1995	The results of a structure-activity relationship study focusing on the interaction of a series of phthalimide and saccharin derivatives with leukocyte elastase, cathepsin G and proteinase 3 are described.	Saccharin	114-123	proteinase 3	Homo sapiens	177-189