PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
7956723-6	1994	Diallyl sulfide, a selective, mechanism-based inhibitor of cytochrome P450 2E1, inhibited the metabolism of HCFC-123, as indicated by a decreased uptake of HCFC-123 and by a lowered urinary excretion of trifluoroacetic acid in diallyl sulfide-treated rats.	Trifluoroacetic Acid	203-223	cytochrome P450, family 2, subfamily e, polypeptide 1	Rattus norvegicus	59-78	
12803597-8	2003	RESULTS: CYP2E1 induction increased both TFA and TFA-protein formation compared with uninduced halothane-treated rats.	Trifluoroacetic Acid	41-44	cytochrome P450, family 2, subfamily e, polypeptide 1	Rattus norvegicus	9-15	
12803597-8	2003	RESULTS: CYP2E1 induction increased both TFA and TFA-protein formation compared with uninduced halothane-treated rats.	Trifluoroacetic Acid	49-52	cytochrome P450, family 2, subfamily e, polypeptide 1	Rattus norvegicus	9-15	
12919728-8	2003	The increase in CYP2E1 apoprotein and p-NPH activity observed in testis and liver microsomes suggests that halothane induces its own biotransformation both hepatically and extrahepatically and in addition, that the nature of the TFA adducts will depend on the proteins present in each tissue.	Trifluoroacetic Acid	229-232	cytochrome P450, family 2, subfamily e, polypeptide 1	Rattus norvegicus	16-22