PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
2495173-3	1989	For several samples of urinary bladder epithelium, prostatic epithelium, colonic mucosa, and peripheral lung tissue, an arachidonic acid-dependent, microsomal-catalyzed activation of benzidine was observed; and the activity could be inhibited appreciably by indomethacin, a known inhibitor of PHS.	benzidine	183-192	pterin-4 alpha-carbinolamine dehydratase 1	Homo sapiens	293-296	
2495173-6	1989	Purified PHS catalyzed the activation of benzidine much greater than 2-naphthylamine, 2-amino-6-methyldipyrido[1,2-alpha:3",2"-d]imidazole greater than 4-aminobiphenyl greater than 2-amino-3-methylimidazo[4,5-f]quinoline greater than 3-amino-1-methyl-5H-pyrido[4,3-b] indole.	benzidine	41-50	pterin-4 alpha-carbinolamine dehydratase 1	Homo sapiens	9-12	
6418878-0	1983	Prostaglandin H synthase-catalyzed activation of benzidine: a model to assess pharmacologic intervention of the initiation of chemical carcinogenesis.	benzidine	49-58	pterin-4 alpha-carbinolamine dehydratase 1	Homo sapiens	0-24	
6418878-3	1983	The procarcinogen benzidine was used to identify sites at which microsomal PHS-catalyzed binding might be inhibited by pharmacologic agents.	benzidine	18-27	pterin-4 alpha-carbinolamine dehydratase 1	Homo sapiens	75-78	
6418878-6	1983	This study provides the first demonstration of inhibition of PHS-activated benzidine binding by propylthiouracil, methimazole, MK447, vitamin C and phenidone.	benzidine	75-84	pterin-4 alpha-carbinolamine dehydratase 1	Homo sapiens	61-64	
6418878-7	1983	The agents tested identified the following sites at which PHS-catalyzed binding of benzidine can be prevented: 1) inhibition of generation of the peroxide cosubstrate for benzidine oxidation; 2) inhibition of prostaglandin hydroperoxidase; 3) reduction of oxidized intermediate(s) to the parent compound; and 4) conjugation of the activated intermediate(s).	benzidine	83-92	pterin-4 alpha-carbinolamine dehydratase 1	Homo sapiens	58-61	
6418878-7	1983	The agents tested identified the following sites at which PHS-catalyzed binding of benzidine can be prevented: 1) inhibition of generation of the peroxide cosubstrate for benzidine oxidation; 2) inhibition of prostaglandin hydroperoxidase; 3) reduction of oxidized intermediate(s) to the parent compound; and 4) conjugation of the activated intermediate(s).	benzidine	171-180	pterin-4 alpha-carbinolamine dehydratase 1	Homo sapiens	58-61