PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25820021-5	2015	Olmesartan uptake via OAT4 was concentration dependent with a Km of 20 muM, and was increased in the absence of chloride.	olmesartan	0-10	solute carrier family 22 member 11	Homo sapiens	22-26	
25820021-6	2015	[(3) H]Olmesartan efflux via OAT4 was also observed and was trans-stimulated by extracellular chloride and DHEAS.	olmesartan	7-17	solute carrier family 22 member 11	Homo sapiens	29-33	
25820021-8	2015	Efflux transport of olmesartan via OAT4 from syncytiotrophoblasts to the fetal circulation might be facilitated in the presence of an inwardly directed physiological chloride gradient and extracellular DHEAS.	olmesartan	20-30	solute carrier family 22 member 11	Homo sapiens	35-39	
33189558-1	2021	Organic anion transporter (OAT) 4, which is localized at the apical membrane of human renal proximal tubules, transports olmesartan, an angiotensin II receptor blocker (ARB).	olmesartan	121-131	solute carrier family 22 member 11	Homo sapiens	0-33	
33189558-2	2021	Many ARBs, including olmesartan, undergo partial tubular secretion as active forms, and inhibit OAT4-mediated uptake activity.	olmesartan	21-31	solute carrier family 22 member 11	Homo sapiens	96-100	
33189558-7	2021	Our results suggest that OAT4 may play a role in the excretion of azilsartan, candesartan, carboxylosartan, and valsartan, as well as olmesartan.	olmesartan	134-144	solute carrier family 22 member 11	Homo sapiens	25-29