PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10030456-4	1998	The specificity of the induction by 4-methylpyrazole and of the inhibition by diallyl sulfide for CYP2E1 was determined using the [14C]caffeine (CYP1A2), [14C]aminopyrine (CYP2C11), and [14C]erythromycin (CYP3A2) breath tests.	Aminopyrine	159-170	cytochrome P450, family 2, subfamily e, polypeptide 1	Rattus norvegicus	98-104	
1538706-11	1992	The metabolism of this compound was strongly inhibited by the CYP2E1 substrates or inhibitors dimethylsulfoxide (1-100 mM), p-nitrophenol (100 microM), and diethyldithiocarbamate (100 microM), which did not affect aminopyrine N-demethylation.	Aminopyrine	214-225	cytochrome P450, family 2, subfamily e, polypeptide 1	Rattus norvegicus	62-68	
1445245-4	1992	In a reconstituted system, ha P-450j showed relatively low catalytic activities towards 7-ethoxycoumarin, 7-ethoxyresorufin, aminopyrine, ethylmorphine and benzphetamine, whereas it catalysed the oxidation of aniline, acetone and thiobenzamide with a high catalytic-centre activity.	Aminopyrine	125-136	cytochrome P450, family 2, subfamily e, polypeptide 1	Rattus norvegicus	30-36	
18710030-4	2008	A high-fat diet enhanced reactions of biotransformation of amidopyrine, acetanilide, toluene, sulfadimezine, were catalyzed with CYP2E1, CYP3A and enzymes of conjugation, simultaneously it increased the hepatotoxicity of paracetamol.	Aminopyrine	59-70	cytochrome P450, family 2, subfamily e, polypeptide 1	Rattus norvegicus	129-135