PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18229607-5	2007	Furthermore, the metabolism of neferine in rat liver microsomes showed that the percentage inhibition of the major metabolism (liensinine) formation was 80.5% by quinidine (10 micromol x L(-1), selective CYP2D1 inhibitor) and 25.7% by ketoconazole (1 micromol x L(-1), selective CYP3A1 inhibitor).	liensinine	127-137	cytochrome P450, family 2, subfamily d, polypeptide 1	Rattus norvegicus	204-210	
18229607-6	2007	Neferine was mainly metabolized by CYP2D1 or CYP3A1 to liensinine, isoliensinine, desmethyl-liensinine and desmethyl-isoliensinine.	liensinine	55-65	cytochrome P450, family 2, subfamily d, polypeptide 1	Rattus norvegicus	35-41