PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
10444235-6	1999	In fact, other molecules such as cetirizine, loratadine, acrivastine, and fexofenadine seem to lack both cardiotoxic potential and HERG-blocking ability at therapeutically relevant concentrations.	fexofenadine	74-86	potassium voltage-gated channel subfamily H member 2	Homo sapiens	131-135	
19204737-8	2009	Coculture with fexofenadine(1 microM), an MDR1 substrate known to rescue misfolding in other membrane proteins, restored cell surface expression of MDR1 G2677T/C3435T and restored resistance to block HERG by ibutilide 200 nM (98.5+/-0.98% vs 42.3+/-2.2%, P<0.001).	fexofenadine	15-27	potassium voltage-gated channel subfamily H member 2	Homo sapiens	200-204	
12411421-5	2002	In the present study the ability of fexofenadine to block the K897T HERG channel variant was investigated.	fexofenadine	36-48	potassium voltage-gated channel subfamily H member 2	Homo sapiens	68-72	
12070109-5	2002	We tested terfenadine carboxylate (fexofenadine) and terfenadine, structurally similar drugs with markedly different affinities for HERG block, for rescue of trafficking-defective LQT2 mutations.	fexofenadine	10-33	potassium voltage-gated channel subfamily H member 2	Homo sapiens	180-184