IndraLab

Statements



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"Interestingly, 10 μM ICA (3-nitro-N-[4-phenoxyphenyl]-benzamide) activated hERG1 and modulated tails, while inhibited hEAG at 3 μM. Both channels in the presence of ICA show a similar inactivation."

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"The hERG activator ICA‐105574 shows structural similarities with LUF7244 and has been analysed in anaesthetized dogs at 1 and 10 mg·"

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"The same concatenation strategy used to characterize PD was used to study ICA, a compound which enhances hERG1 current by strongly inhibiting channel inactivation."

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"ICA strongly inhibits inactivation and thereby increases the magnitude of hERG1 channel currents, especially at positive potentials."

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"We took advantage of our previous finding that L646E and F557L mutations nearly abolish the ability of PD and ICA, respectively, to enhance hERG1 currents."

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"ICA increases the magnitude of outward hERG1 currents by profound attenuation of inactivation."