PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
4033629-3	1985	Of eight major cytochrome P-450 isozymes which could be monitored in this fashion, three were inhibited by more than 50% by a dose of chloramphenicol of 300 mg/kg, whereas no evidence of inhibition of the remaining isozymes was obtained.	Chloramphenicol	134-149	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	15-31	
4033629-4	1985	P-450PB-C, an isozyme which is present in significant amounts in untreated rats and which is induced approximately 2-fold by phenobarbital, was the most susceptible cytochrome P-450 to inhibition by chloramphenicol both in vivo and in vitro.	Phenobarbital	125-138	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	165-181	
4033629-4	1985	P-450PB-C, an isozyme which is present in significant amounts in untreated rats and which is induced approximately 2-fold by phenobarbital, was the most susceptible cytochrome P-450 to inhibition by chloramphenicol both in vivo and in vitro.	Chloramphenicol	199-214	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	165-181	
4033629-5	1985	P-450PB-B, the major phenobarbital-inducible isozyme, and P-450UT-A, a male-specific testosterone 2 alpha- and 16 alpha-hydroxylase, were intermediate in their susceptibility to chloramphenicol.	Chloramphenicol	178-193	cytochrome P450, subfamily 2, polypeptide 11	Rattus norvegicus	58-67