PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
20135098-6	2010	On the other, the evoked release of ATP was greatly reduced by multidrug resistance protein (MRP) transporter inhibitors, MK-571, indomethacin, and benzbromarone.	Benzbromarone	148-161	ATP binding cassette subfamily C member 1	Homo sapiens	63-91	
20135098-6	2010	On the other, the evoked release of ATP was greatly reduced by multidrug resistance protein (MRP) transporter inhibitors, MK-571, indomethacin, and benzbromarone.	Benzbromarone	148-161	ATP binding cassette subfamily C member 1	Homo sapiens	93-96	
15041471-8	2004	Benzbromarone, a specific MRP1 inhibitor, decreased the initial efflux rate in 2008/MRP1 cells (4-fold) and in 2008wt cells (2-fold).	Benzbromarone	0-13	ATP binding cassette subfamily C member 1	Homo sapiens	26-30	
15041471-8	2004	Benzbromarone, a specific MRP1 inhibitor, decreased the initial efflux rate in 2008/MRP1 cells (4-fold) and in 2008wt cells (2-fold).	Benzbromarone	0-13	ATP binding cassette subfamily C member 1	Homo sapiens	84-88	
17710652-5	2007	The inhibition profiles of cyclosporin A, verapamil, benzbromarone, and probenecid in erythrocyte membrane vesicles were typical for MRP1-mediated transport.	Benzbromarone	53-66	ATP binding cassette subfamily C member 1	Homo sapiens	133-137	
11880368-5	2002	Organic anions (probenecid, benzbromarone, indomethacin), known to interfere with glutathione conjugate transport of human ABCC1 and ABCC2, inhibited the ABCC6-mediated NEM-GS transport in a specific manner, indicating that ABCC6 has a unique substrate specificity.	Benzbromarone	28-41	ATP binding cassette subfamily C member 1	Homo sapiens	123-128