PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
30652318-5	2019	In contrast, atorvastatin, bosentan, etoposide, fexofenadine, fluvastatin, glibenclamide and simeprevir were broadly transported by recombinant monkey OATP1B1, OATP1B3 and OATP2B1.	fexofenadine	48-60	solute carrier organic anion transporter family member 1B3	Homo sapiens	160-167	
29635947-9	2018	Rifampicin significantly increases plasma concentrations of both enantiomers through inhibition of OATP1B3, whereas enantioselectivity of fexofenadine uptake by OATP1B3-expressing cells has not been observed.	fexofenadine	138-150	solute carrier organic anion transporter family member 1B3	Homo sapiens	161-168	
16455804-6	2006	Inhibition potency of probenecid for the uptake of fexofenadine was compared between hOAT3 and organic anion-transporting peptide 1B3 (hOATP1B3), a transporter responsible for the hepatic uptake of fexofenadine (Drug Metab Dispos 33:1477-1481, 2005).	fexofenadine	198-210	solute carrier organic anion transporter family member 1B3	Homo sapiens	135-143	
23115085-5	2013	Rifampicin inhibited the uptake of fexofenadine enantiomers by human hepatocytes via organic anion transporter (OAT) OATP1B3 and its basal-to-apical transport in Caco-2 cells, but not OAT3-mediated or multidrug and toxic compound extrusion 1 (MATE1)-mediated transport.	fexofenadine	35-47	solute carrier organic anion transporter family member 1B3	Homo sapiens	117-124	
18180276-6	2008	Vectorial basal-to-apical transport of FEX was observed in double transfectants expressing OATP1B1/multidrug resistance-associated protein 2 (MRP2) and OATP1B3/MRP2, suggesting that OATP1B1 as well as OATP1B3 is involved in the hepatic uptake of FEX and that MRP2 can recognize FEX as a substrate.	fexofenadine	39-42	solute carrier organic anion transporter family member 1B3	Homo sapiens	152-159	
18180276-6	2008	Vectorial basal-to-apical transport of FEX was observed in double transfectants expressing OATP1B1/multidrug resistance-associated protein 2 (MRP2) and OATP1B3/MRP2, suggesting that OATP1B1 as well as OATP1B3 is involved in the hepatic uptake of FEX and that MRP2 can recognize FEX as a substrate.	fexofenadine	39-42	solute carrier organic anion transporter family member 1B3	Homo sapiens	201-208	
18180276-7	2008	The inhibitory effects of compounds on FEX uptake in OATP1B3-expressing HEK293 cells were investigated, and the maximal degree of increase in plasma AUC of FEX by drug interaction in clinical situations was estimated.	fexofenadine	39-42	solute carrier organic anion transporter family member 1B3	Homo sapiens	53-60	
16014768-12	2005	In conclusion, this is, to our knowledge, the first demonstration that OATP1B3 is thought to be a major transporter involved in hepatic uptake of FEX in humans.	fexofenadine	146-149	solute carrier organic anion transporter family member 1B3	Homo sapiens	71-78