PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25656918-3	2015	The results from single point time dependent inhibition and shift assays suggest that clorgyline, pargyline, phenelzine, and selegiline were metabolism based inhibitors of CYP2B6.	Phenelzine	109-119	cytochrome P450 family 2 subfamily B member 6	Homo sapiens	172-178	
25656918-4	2015	In IC50 shift assays, clorgyline, pargyline, phenelzine and selegiline are metabolism based inhibitors of CYP2B6 with fold shit of 3.0-, 3.7-, 2.9-, and 11.4-fold respectively.	Phenelzine	45-55	cytochrome P450 family 2 subfamily B member 6	Homo sapiens	106-112	
25656918-6	2015	Phenelzine inactivated CYP2B6 with KI and k(inact) values of 44.9 +- 6.9 muM and 0.085 +- 0.003 min(-1) respectively.	Phenelzine	0-10	cytochrome P450 family 2 subfamily B member 6	Homo sapiens	23-29	
25656918-13	2015	Caution is required while co-administering phenelzine with substrates that are exclusively metabolized by CYP2B6 enzyme and substrates that have narrow therapeutic index.	Phenelzine	43-53	cytochrome P450 family 2 subfamily B member 6	Homo sapiens	106-112