IndraLab

Statements



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"Notably, in vitro experiments showed that BZT potently inhibited acetylcholine (ACh)-induced responses mediated by α7 (IC =122 nM) and α4β2 (IC =49 nM) nicotinic ACh receptors (nAChRs), the M1 muscarinic ACh receptor (IC =40 nM; mAChR), as well as the human ether-a-go-go-related gene (hERG) channel (IC =17 nM)."

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"Use dependent inhibition of HERG channels by tetra-n-octylammonium bromide and benzethonium chloride."

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"The properties of HERG channel inhibition by tetra-n-octylammonium bromide and benzethonium chloride are highly similar to verapamil and cisapride (XREF_TABLE)."

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"In summary, our results demonstrate that tetra-n-octylammonium bromide and benzethonium chloride inhibit HERG channel currents in the voltage dependent and use dependent manners."

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"The study of mechanism of HERG channel inhibition by tetra-n-octylammonium bromide and benzethonium chloride can provide additional insight of structure activity relationship of HERG channel inhibition and the molecular determinants of the interaction between the compounds and HERG channel proteins."

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"In this study, we found that benzethonium chloride, domiphen bromide, and tetra-n-octylammonium bromide significantly inhibited hERG channel activity in both the thallium influx assay and the patch clamp experiment."

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"In the present study, the potential mechanisms for HERG channel inhibition by tetra-n-octylammonium bromide and benzethonium chloride, two most potent HERG channel inhibitors found among the QACs examined, were studied using whole-cell patch clamp experiments in a CHO cell line stably expressing HERG channels."

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"Our data indicated that tetra-n-octylammonium bromide blocks HERG channels in both open and inactivated states (XREF_FIG), whereas benzethonium chloride preferentially blocks HERG channels in the open states."

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"Concentration dependent inhibition of HERG channel by tetra-n-octylammonium bromide and benzethonium chloride."