PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
7728897-0	1995	Characterization of hepatic microsomal cytochrome P-450 from rats treated with methylsulphonyl metabolites of polychlorinated biphenyl congeners.	diphenyl	126-134	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	39-55	
7728897-4	1995	Major PB-inducible forms, CYP2B1, CYP2B2, CYP3A2 and CYP2C6 were induced with four PCBs (342 mumol/kg) and their 3-MeSO2 metabolites (0.5-10 mumol/kg), indicating that 3-MeSO2 metabolites were strong PB-type inducers of hepatic drug-metabolizing enzymes.	Polychlorinated Biphenyls	83-87	cytochrome P450, family 2, subfamily b, polypeptide 1	Rattus norvegicus	26-32	
7728897-4	1995	Major PB-inducible forms, CYP2B1, CYP2B2, CYP3A2 and CYP2C6 were induced with four PCBs (342 mumol/kg) and their 3-MeSO2 metabolites (0.5-10 mumol/kg), indicating that 3-MeSO2 metabolites were strong PB-type inducers of hepatic drug-metabolizing enzymes.	Polychlorinated Biphenyls	83-87	cytochrome P450, family 2, subfamily b, polypeptide 2	Rattus norvegicus	34-40	
7728897-4	1995	Major PB-inducible forms, CYP2B1, CYP2B2, CYP3A2 and CYP2C6 were induced with four PCBs (342 mumol/kg) and their 3-MeSO2 metabolites (0.5-10 mumol/kg), indicating that 3-MeSO2 metabolites were strong PB-type inducers of hepatic drug-metabolizing enzymes.	Polychlorinated Biphenyls	83-87	cytochrome P450, family 3, subfamily a, polypeptide 2	Rattus norvegicus	42-48	
7728897-4	1995	Major PB-inducible forms, CYP2B1, CYP2B2, CYP3A2 and CYP2C6 were induced with four PCBs (342 mumol/kg) and their 3-MeSO2 metabolites (0.5-10 mumol/kg), indicating that 3-MeSO2 metabolites were strong PB-type inducers of hepatic drug-metabolizing enzymes.	Polychlorinated Biphenyls	83-87	cytochrome P450, family 2, subfamily C, polypeptide 6, variant 1	Rattus norvegicus	53-59	
7728897-4	1995	Major PB-inducible forms, CYP2B1, CYP2B2, CYP3A2 and CYP2C6 were induced with four PCBs (342 mumol/kg) and their 3-MeSO2 metabolites (0.5-10 mumol/kg), indicating that 3-MeSO2 metabolites were strong PB-type inducers of hepatic drug-metabolizing enzymes.	3-meso2	113-120	cytochrome P450, family 2, subfamily b, polypeptide 2	Rattus norvegicus	34-40	
7728897-4	1995	Major PB-inducible forms, CYP2B1, CYP2B2, CYP3A2 and CYP2C6 were induced with four PCBs (342 mumol/kg) and their 3-MeSO2 metabolites (0.5-10 mumol/kg), indicating that 3-MeSO2 metabolites were strong PB-type inducers of hepatic drug-metabolizing enzymes.	3-meso2	113-120	cytochrome P450, family 3, subfamily a, polypeptide 2	Rattus norvegicus	42-48	
7728897-6	1995	On the other hand, four PB-inducible forms of cytochrome P-450 were not induced with the 4-MeSO2 isomers.	Phenobarbital	24-26	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	46-62	
7728897-7	1995	The relation between liver concentrations of the corresponding 3-MeSO2 derivatives and induction of four PB-inducible forms of cytochrome P-450 after administration of four PCBs and their 3-MeSO2 derivatives further confirmed that the 3-MeSO2 metabolites played an important role in the induction which parent PCB congeners caused on the hepatic drug-metabolizing enzyme system.	3-meso2	63-70	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	127-143	
7728897-7	1995	The relation between liver concentrations of the corresponding 3-MeSO2 derivatives and induction of four PB-inducible forms of cytochrome P-450 after administration of four PCBs and their 3-MeSO2 derivatives further confirmed that the 3-MeSO2 metabolites played an important role in the induction which parent PCB congeners caused on the hepatic drug-metabolizing enzyme system.	3-meso2	63-70	pyruvate carboxylase	Rattus norvegicus	173-176	
7728897-7	1995	The relation between liver concentrations of the corresponding 3-MeSO2 derivatives and induction of four PB-inducible forms of cytochrome P-450 after administration of four PCBs and their 3-MeSO2 derivatives further confirmed that the 3-MeSO2 metabolites played an important role in the induction which parent PCB congeners caused on the hepatic drug-metabolizing enzyme system.	Phenobarbital	105-107	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	127-143	
7728897-7	1995	The relation between liver concentrations of the corresponding 3-MeSO2 derivatives and induction of four PB-inducible forms of cytochrome P-450 after administration of four PCBs and their 3-MeSO2 derivatives further confirmed that the 3-MeSO2 metabolites played an important role in the induction which parent PCB congeners caused on the hepatic drug-metabolizing enzyme system.	Phenobarbital	105-107	pyruvate carboxylase	Rattus norvegicus	173-176	
7728897-7	1995	The relation between liver concentrations of the corresponding 3-MeSO2 derivatives and induction of four PB-inducible forms of cytochrome P-450 after administration of four PCBs and their 3-MeSO2 derivatives further confirmed that the 3-MeSO2 metabolites played an important role in the induction which parent PCB congeners caused on the hepatic drug-metabolizing enzyme system.	Polychlorinated Biphenyls	173-177	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	127-143	
7728897-7	1995	The relation between liver concentrations of the corresponding 3-MeSO2 derivatives and induction of four PB-inducible forms of cytochrome P-450 after administration of four PCBs and their 3-MeSO2 derivatives further confirmed that the 3-MeSO2 metabolites played an important role in the induction which parent PCB congeners caused on the hepatic drug-metabolizing enzyme system.	3-meso2	188-195	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	127-143	
7728897-7	1995	The relation between liver concentrations of the corresponding 3-MeSO2 derivatives and induction of four PB-inducible forms of cytochrome P-450 after administration of four PCBs and their 3-MeSO2 derivatives further confirmed that the 3-MeSO2 metabolites played an important role in the induction which parent PCB congeners caused on the hepatic drug-metabolizing enzyme system.	3-meso2	188-195	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	127-143