PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15900017-11	2005	These results suggest that rOat2 accounts partly for the hepatic uptake of ketoprofen and, presumably, indomethacin as a high-affinity site and that other transporters, such as rOatps, but not rOatp2, and rOat3, are also involved.	Ketoprofen	75-85	solute carrier family 22 member 7	Rattus norvegicus	27-32	
15900017-0	2005	Functional involvement of rat organic anion transporter 2 (Slc22a7) in the hepatic uptake of the nonsteroidal anti-inflammatory drug ketoprofen.	Ketoprofen	133-143	solute carrier family 22 member 7	Rattus norvegicus	30-57	
15900017-0	2005	Functional involvement of rat organic anion transporter 2 (Slc22a7) in the hepatic uptake of the nonsteroidal anti-inflammatory drug ketoprofen.	Ketoprofen	133-143	solute carrier family 22 member 7	Rattus norvegicus	59-66	
15900017-3	2005	rOat2 substrates include nonsteroidal anti-inflammatory drugs, such as ketoprofen, indomethacin, and salicylate.	Ketoprofen	71-81	solute carrier family 22 member 7	Rattus norvegicus	0-5	
15900017-3	2005	rOat2 substrates include nonsteroidal anti-inflammatory drugs, such as ketoprofen, indomethacin, and salicylate.	Indomethacin	83-95	solute carrier family 22 member 7	Rattus norvegicus	0-5	
15900017-3	2005	rOat2 substrates include nonsteroidal anti-inflammatory drugs, such as ketoprofen, indomethacin, and salicylate.	Salicylates	101-111	solute carrier family 22 member 7	Rattus norvegicus	0-5	
15900017-8	2005	The K(m) values of the high-affinity component were similar to those for rOat2 (3.3 and 0.37 microM for ketoprofen and indomethacin, respectively).	Ketoprofen	104-114	solute carrier family 22 member 7	Rattus norvegicus	73-78	
15900017-8	2005	The K(m) values of the high-affinity component were similar to those for rOat2 (3.3 and 0.37 microM for ketoprofen and indomethacin, respectively).	Indomethacin	119-131	solute carrier family 22 member 7	Rattus norvegicus	73-78	
15900017-9	2005	The uptake of ketoprofen by hepatocytes was significantly inhibited by probenecid and rOat2 inhibitors (indocyanine green, indomethacin, glibenclamide, and salicylate).	Ketoprofen	14-24	solute carrier family 22 member 7	Rattus norvegicus	86-91	
15900017-9	2005	The uptake of ketoprofen by hepatocytes was significantly inhibited by probenecid and rOat2 inhibitors (indocyanine green, indomethacin, glibenclamide, and salicylate).	Indocyanine Green	104-121	solute carrier family 22 member 7	Rattus norvegicus	86-91	
15900017-9	2005	The uptake of ketoprofen by hepatocytes was significantly inhibited by probenecid and rOat2 inhibitors (indocyanine green, indomethacin, glibenclamide, and salicylate).	Indomethacin	123-135	solute carrier family 22 member 7	Rattus norvegicus	86-91	
15900017-9	2005	The uptake of ketoprofen by hepatocytes was significantly inhibited by probenecid and rOat2 inhibitors (indocyanine green, indomethacin, glibenclamide, and salicylate).	Glyburide	137-150	solute carrier family 22 member 7	Rattus norvegicus	86-91	
15900017-9	2005	The uptake of ketoprofen by hepatocytes was significantly inhibited by probenecid and rOat2 inhibitors (indocyanine green, indomethacin, glibenclamide, and salicylate).	Salicylates	156-166	solute carrier family 22 member 7	Rattus norvegicus	86-91	
15900017-10	2005	Other inhibitors of rOatps (taurocholate and pravastatin) and rOat3 (pravastatin and p-aminohippurate) had a slight effect, but digoxin had no effect.	Pravastatin	69-80	solute carrier family 22 member 8	Rattus norvegicus	62-67	
15900017-10	2005	Other inhibitors of rOatps (taurocholate and pravastatin) and rOat3 (pravastatin and p-aminohippurate) had a slight effect, but digoxin had no effect.	p-Aminohippuric Acid	85-101	solute carrier family 22 member 8	Rattus norvegicus	62-67	
15900017-11	2005	These results suggest that rOat2 accounts partly for the hepatic uptake of ketoprofen and, presumably, indomethacin as a high-affinity site and that other transporters, such as rOatps, but not rOatp2, and rOat3, are also involved.	Ketoprofen	75-85	solute carrier family 22 member 8	Rattus norvegicus	205-210	
15900017-11	2005	These results suggest that rOat2 accounts partly for the hepatic uptake of ketoprofen and, presumably, indomethacin as a high-affinity site and that other transporters, such as rOatps, but not rOatp2, and rOat3, are also involved.	Indomethacin	103-115	solute carrier family 22 member 7	Rattus norvegicus	27-32	
15900017-11	2005	These results suggest that rOat2 accounts partly for the hepatic uptake of ketoprofen and, presumably, indomethacin as a high-affinity site and that other transporters, such as rOatps, but not rOatp2, and rOat3, are also involved.	Indomethacin	103-115	solute carrier family 22 member 8	Rattus norvegicus	205-210	
15900017-11	2005	These results suggest that rOat2 accounts partly for the hepatic uptake of ketoprofen and, presumably, indomethacin as a high-affinity site and that other transporters, such as rOatps, but not rOatp2, and rOat3, are also involved.	roatps	177-183	solute carrier family 22 member 8	Rattus norvegicus	205-210