PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
28215170-2	2017	OBJECTIVES: The aim of the current study was to investigate the antiglycation activity of nitrobenzimidazole derivatives against fructose-mediated human serum albumin (HSA) glycation.	2-Nitro-1H-benzo[d]imidazole	90-108	albumin	Mus musculus	153-166
20163895-3	2010	Compounds 6c and 6h with nitrobenzimidazole and pyrimidyl heterocycles attached at 5th position via sulfur were the most potent of all with IC50 values approximately 17.6 muM.	2-Nitro-1H-benzo[d]imidazole	25-43	latexin	Homo sapiens	171-174
9343369-8	1997	That points out to partial determination of nitrobenzimidazole cytotoxicity by their reduction by DT-diaphorase.	2-Nitro-1H-benzo[d]imidazole	44-62	NAD(P)H quinone dehydrogenase 1	Homo sapiens	98-111