PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
12665390-6	2003	Atypical antipsychotics are metabolised predominantly by cytochrome p450 (CYP) isoenzymes, particularly CYP1A2 (clozapine and olanzapine), CYP3A4 (clozapine, quetiapine and ziprasidone) and CYP2D6 (olanzapine and risperidone).	ziprasidone	173-184	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	57-72	
12665390-6	2003	Atypical antipsychotics are metabolised predominantly by cytochrome p450 (CYP) isoenzymes, particularly CYP1A2 (clozapine and olanzapine), CYP3A4 (clozapine, quetiapine and ziprasidone) and CYP2D6 (olanzapine and risperidone).	ziprasidone	173-184	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	74-77	
10771452-13	2000	CONCLUSIONS: Ziprasidone is predominantly metabolized by CYP3A4 in human liver microsomes and is not expected to mediate drug interactions with coadministered CYP substrates, at clinically effective doses.	ziprasidone	13-24	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	57-60	
10771452-0	2000	Identification of the major human liver cytochrome P450 isoform(s) responsible for the formation of the primary metabolites of ziprasidone and prediction of possible drug interactions.	ziprasidone	127-138	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	40-55	
10771452-1	2000	AIMS: To identify the cytochrome P450 (CYP) isoform(s) responsible for the formation of the primary metabolite of ziprasidone (ziprasidone sulphoxide), to determine the kinetics of its formation and to predict possible drug interactions by investigating CYP isoform inhibition in an in vitro study.	ziprasidone	114-125	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	22-37	
10771452-1	2000	AIMS: To identify the cytochrome P450 (CYP) isoform(s) responsible for the formation of the primary metabolite of ziprasidone (ziprasidone sulphoxide), to determine the kinetics of its formation and to predict possible drug interactions by investigating CYP isoform inhibition in an in vitro study.	ziprasidone	114-125	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	39-42	
10771452-1	2000	AIMS: To identify the cytochrome P450 (CYP) isoform(s) responsible for the formation of the primary metabolite of ziprasidone (ziprasidone sulphoxide), to determine the kinetics of its formation and to predict possible drug interactions by investigating CYP isoform inhibition in an in vitro study.	ziprasidone	114-125	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	254-257