PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 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 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 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 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 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 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 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 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