PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
2355308-6	1990	These results suggest that danazol is a highly potent inhibitor for several cytochrome P-450-mediated metabolisms of testosterone and xenobiotics in mouse hepatic microsomes.	Danazol	27-34	cytochrome P450, family 21, subfamily a, polypeptide 1	Mus musculus	76-92	
2355308-0	1990	[Inhibition of cytochrome P-450-dependent monoxygenase activities by a synthetic androgen danazol in mouse hepatic microsomes].	Danazol	90-97	cytochrome P450, family 21, subfamily a, polypeptide 1	Mus musculus	15-31	
2355308-4	1990	Addition of danazol to microsomal preparation resulted in a reverse type I difference spectrum and the spectrophotometric analysis revealed that danazol had a high affinity for cytochrome P-450 with dissociation constants (Ks) of 0.9 and 4.2 microM, which were 2 orders of magnitude lower than those of cimetidine.	Danazol	12-19	cytochrome P450, family 21, subfamily a, polypeptide 1	Mus musculus	177-193	
2355308-4	1990	Addition of danazol to microsomal preparation resulted in a reverse type I difference spectrum and the spectrophotometric analysis revealed that danazol had a high affinity for cytochrome P-450 with dissociation constants (Ks) of 0.9 and 4.2 microM, which were 2 orders of magnitude lower than those of cimetidine.	Danazol	145-152	cytochrome P450, family 21, subfamily a, polypeptide 1	Mus musculus	177-193