PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20501911-3	2010	The kinetics of metabolite formation from phenacetin, tolbutamide, and alprazolam and midazolam, selected as substrates probes for CYP1A2, CYP2C9, and CYP3A4, respectively, were characterized in this in vitro system.	Alprazolam	71-81	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	131-137	
20080160-9	2010	In conclusion, Alprazolam, Bromazepam, Chlordiazepoxide, Clonazepam, Diazepam, Lorazepam, Nitrazepam, Oxazepam, Tetrazepam and Triazolam can be considered as safe drugs in term of their inability to induce PXR- and AhR-dependent cytochrome P450 enzymes CYP1A2 and CYP3A4.	Alprazolam	15-25	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	253-259	
9435993-20	1997	CYP2C19 and CYP1A2, the metabolism of several benzodiazepines, including alprazolam, bromazepam and diazepam.	Alprazolam	73-83	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	12-18	
10634135-0	1999	Simultaneous assessment of CYP3A4 and CYP1A2 activity in vivo with alprazolam and caffeine.	Alprazolam	67-77	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	38-44	
10634135-1	1999	Alprazolam (ALP) and caffeine (CAF) were suggested as probe drugs for the activities of CYP3A4 and CYP1A2, respectively.	Alprazolam	0-10	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	99-105	
10634135-1	1999	Alprazolam (ALP) and caffeine (CAF) were suggested as probe drugs for the activities of CYP3A4 and CYP1A2, respectively.	Alprazolam	12-15	cytochrome P450 family 1 subfamily A member 2	Homo sapiens	99-105