PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
29759885-4	2018	Among the four CYP2J2 inhibitors tested, terfenadone was strongest inhibitor of CYP2J2-mediated metabolism of albendazole, astemizole, and terfenadine with IC50 values of 0.31, 0.15, and 2.11 muM, respectively, in human liver microsomes (HLMs).	Terfenadine	139-150	latexin	Homo sapiens	192-195	
24120820-5	2013	Terfenadine also showed a limited solubility (measured concentrations ranging from 0.597 muM to 0.833 muM instead of 1 muM) and a loss of substance through the superfusion tubing from -30.2% to -39.2% with dimethylsulfoxide, ethanol or methanol.	Terfenadine	0-11	latexin	Homo sapiens	89-92	
24120820-5	2013	Terfenadine also showed a limited solubility (measured concentrations ranging from 0.597 muM to 0.833 muM instead of 1 muM) and a loss of substance through the superfusion tubing from -30.2% to -39.2% with dimethylsulfoxide, ethanol or methanol.	Terfenadine	0-11	latexin	Homo sapiens	102-105	
24120820-5	2013	Terfenadine also showed a limited solubility (measured concentrations ranging from 0.597 muM to 0.833 muM instead of 1 muM) and a loss of substance through the superfusion tubing from -30.2% to -39.2% with dimethylsulfoxide, ethanol or methanol.	Terfenadine	0-11	latexin	Homo sapiens	102-105	
24296992-7	2013	Infusion of 1 muM Dofetilide and 10 muM Terfenadine prolonged field potentials 10 fold and 2 fold, respectively.	Terfenadine	40-51	latexin	Homo sapiens	36-39