PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
23121773-6	2013	The oral antidiabetic drugs glibenclamide, glimepiride and nateglinide inhibited the transport of the model substrate bromosulfophthalein, particularly the OATP2B1-mediated uptake.	Glyburide	28-41	solute carrier organic anion transporter family member 2B1	Homo sapiens	156-163	
24839071-2	2014	Comprehensive in vitro studies suggested that glyburide is a highly permeable drug with substrate affinity to multiple efflux pumps and to organic anion transporting polypeptide (OATP)1B1 and OATP2B1.	Glyburide	46-55	solute carrier organic anion transporter family member 2B1	Homo sapiens	192-199	
23121773-8	2013	For glibenclamide, inhibitory constants (Ki values) of 13.6 muM, 8.1 muM and 0.5 muM for OATP1B1-, OATP1B3- and OATP2B1-mediated BSP uptake were determined.	Glyburide	4-17	solute carrier organic anion transporter family member 2B1	Homo sapiens	112-119	
32483763-8	2020	The OATP2B1 inhibitors, including atorvastatin, bromosulfophthalein, glibenclamide, sulfasalazine, talinolol, and estrone 3-sulfate, inhibited the DBF and the 5-CF transport.	Glyburide	69-82	solute carrier organic anion transporter family member 2B1	Homo sapiens	4-11	
15640378-8	2005	Glibenclamide, a hypoglycemic drug, was identified for the first time as a substrate for OATP-B with a K(t) value of 6.26 microM.	Glyburide	0-13	solute carrier organic anion transporter family member 2B1	Homo sapiens	89-95	
15640378-9	2005	GFJ and OJ inhibited the OATP-B-mediated uptake of glibenclamide.	Glyburide	51-64	solute carrier organic anion transporter family member 2B1	Homo sapiens	25-31	
15640378-10	2005	These results suggest that citrus juices may inhibit the intestinal absorption of anionic drugs, such as glibenclamide, via the inhibition of OATP-B.	Glyburide	105-118	solute carrier organic anion transporter family member 2B1	Homo sapiens	142-148	
17178262-8	2006	Furthermore, estrone-3-sulfate transport into OATP2B1-overexpressing Madin-Darby canine kidney II cells was inhibited by various drugs, including atorvastatin, simvastatin, cerivastatin, glyburide (INN, glibenclamide), and gemfibrozil, with the most pronounced effect being found for atorvastatin (inhibition constant, 0.7 +/- 0.4 micromol/L).	Glyburide	187-196	solute carrier organic anion transporter family member 2B1	Homo sapiens	46-53	
17178262-8	2006	Furthermore, estrone-3-sulfate transport into OATP2B1-overexpressing Madin-Darby canine kidney II cells was inhibited by various drugs, including atorvastatin, simvastatin, cerivastatin, glyburide (INN, glibenclamide), and gemfibrozil, with the most pronounced effect being found for atorvastatin (inhibition constant, 0.7 +/- 0.4 micromol/L).	Glyburide	203-216	solute carrier organic anion transporter family member 2B1	Homo sapiens	46-53	
30652318-5	2019	In contrast, atorvastatin, bosentan, etoposide, fexofenadine, fluvastatin, glibenclamide and simeprevir were broadly transported by recombinant monkey OATP1B1, OATP1B3 and OATP2B1.	Glyburide	75-88	solute carrier organic anion transporter family member 2B1	Homo sapiens	172-179