PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15572279-5	2005	Thioridazine (Ki=15 microM) was the most potent inhibitor of the rat CYP2D among the drugs studied, whose effect was more pronounced than that of the other neuroleptics tested: phenothiazines (Ki=18-23 microM), haloperidol (Ki=32 microM), sertindole (Ki=51 microM) or risperidone (Ki=165 microM).	Phenothiazines	177-191	cytochrome P450 family 2 subfamily D member 6	Homo sapiens	69-74	
15572279-8	2005	After chronic treatment with the investigated neuroleptics, the decreased CYP2D activity produced by the phenothiazines was still maintained, while that caused by haloperidol diminished.	Phenothiazines	105-119	cytochrome P450 family 2 subfamily D member 6	Homo sapiens	74-79