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1 he presence of the pharmacological chaperone astemizole.
2 Treatment of hindlimb-suspended mice with astemizole, a known Merg1a channel blocker, inhibits atr
4 imilar findings were obtained with the drugs astemizole and cisapride, as well as with high concentra
5 tro ATPase assays confirmed three (ebastine, astemizole and clotrimazole) out of seven tested candida
6 drugs approved for human use and identified astemizole and tacrolimus, which reduced cell-surface Pr
8 ethylastemizole, the principal metabolite of astemizole, blocks delayed rectifier potassium (K+) chan
10 Cytochrome P450 3A4 metabolizes terfenadine, astemizole, carbamazepine, alprazolam, triazolam, and ot
11 phenotype cells and was inactive in a [(3)H]astemizole competitive binding assay for hERG liability
12 exposure of NRVMs to LUF7244 or LUF7244 plus astemizole did not affect their viability, excitability,
13 mperature for R752W or with the hERG blocker astemizole for G601S dissociates channel-chaperone compl
14 ts and the favorable drug characteristics of astemizole, including its ability to cross the blood-bra
15 n and torsade de pointes are associated with astemizole intake and have been ascribed to block the re
16 olongation and torsade de pointes found with astemizole intake may principally be caused by the proar
18 nt with undetectable serum concentrations of astemizole (< 0.5 ng/ml) and "therapeutic" concentration
20 t ventricular myocyte (NRVM) monolayers with astemizole or sertindole caused heterogeneous prolongati
21 e, exposure to the pharmacological chaperone astemizole, or specific mutations in the selectivity fil
22 inities of typical blockers (ie, dofetilide, astemizole, sertindole, and cisapride) were significantl
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