PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
21782880-12	2011	In Jurkat cells incubated with amiloride (30 muM), the ACO-induced inhibition of I(K(DR)) remained unaltered.	Amiloride	31-40	latexin	Homo sapiens	45-48	
29214230-6	2017	Amiloride (500 muM), ethanol (up to 0.1% v/v), and DMSO (up to 0.1% v/v) did not reduce cell viability nor induce cytotoxicity.	Amiloride	0-9	latexin	Homo sapiens	15-18	
25268680-7	2015	Pharmacological analysis showed that the mechanosensitive channels were potently blocked by amiloride (1mM) and Gd3+ (10 muM) in a voltage-dependent manner.	Amiloride	92-101	latexin	Homo sapiens	121-124	
24553299-10	2014	Importantly, HO-1 induction enhanced migration (43 +- 5% of control, P < 0.05), but the enhanced migratory response was entirely blocked by ENaC inhibition with amiloride (10 muM).	Amiloride	164-173	latexin	Homo sapiens	178-181	
22421400-9	2012	Amiloride (0.3 muM) reduced the acid-evoked ATP release by approximately 70%, while capsazepine (10 muM) reduced acid-evoked ATP release at pH 6.0 and pH 5.6 (by 68% and 61%, respectively).	Amiloride	0-9	latexin	Homo sapiens	15-18	
23085555-3	2012	This current was completely suppressed when 1 muM amiloride was applied before adding the bactridines.	Amiloride	50-59	latexin	Homo sapiens	46-49	
23085555-4	2012	Since the amiloride sensitive current is able to distort the aim of our study, i.e. the effect of bactridines on sodium channels, all experiments were done in the presence of 1 muM amiloride.	Amiloride	10-19	latexin	Homo sapiens	177-180	
22767612-4	2012	By performing whole-cell patch-clamp recordings of human embryonic kidney 293 cells stably expressing human Ca(V)3 channels, we found that amiloride blocked the human Ca(V)3 channels in a concentration-response manner; the IC50 for Ca(V)3.2 channels (62 muM) was 13-fold lower than that for Ca(V)3.1 and Ca(V)3.3.	Amiloride	139-148	latexin	Homo sapiens	254-257	
21978672-1	2011	A known side-activity of the oral potassium-sparing diuretic drug amiloride is inhibition of the enzyme urokinase-type plasminogen activator (uPA, K(i)=7 muM), a promising anticancer target.	Amiloride	66-75	latexin	Homo sapiens	154-157	
19282337-6	2009	In these 3 subjects, an inhibitor of the epithelial sodium channel, amiloride (10 muM), blocked the ability to distinguish salt concentrations and affected the LSP.	Amiloride	68-77	latexin	Homo sapiens	82-85