PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24036158-4	2013	Our results show that at a clinically relevant concentration of 10 muM, mycophenolic acid inhibited both OAT1- and OAT3-mediated [(3)H]-MTX uptake.	Mycophenolic Acid	72-89	solute carrier family 22 member 8	Homo sapiens	115-119	
17526543-11	2007	Human OAT3, but not hOAT1, was additionally inhibited by both glucuronide metabolites of MPA in a concentration-dependent manner (IC50 15.2 microM for MPAG and 2.88 microM for AcMPAG), consistent with a preference of hOAT3 for more bulky substrates compared with hOAT1.	Mycophenolic Acid	89-92	solute carrier family 22 member 8	Homo sapiens	6-10	
17526543-11	2007	Human OAT3, but not hOAT1, was additionally inhibited by both glucuronide metabolites of MPA in a concentration-dependent manner (IC50 15.2 microM for MPAG and 2.88 microM for AcMPAG), consistent with a preference of hOAT3 for more bulky substrates compared with hOAT1.	Mycophenolic Acid	89-92	solute carrier family 22 member 8	Homo sapiens	217-222	
17462604-0	2007	Interaction and transport characteristics of mycophenolic acid and its glucuronide via human organic anion transporters hOAT1 and hOAT3.	Mycophenolic Acid	45-62	solute carrier family 22 member 8	Homo sapiens	130-135