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• W2076271650 abstract "Research into Ca2+-activated Cl- channels is hampered by the inability to decipher their molecular identity and the fact that all extant Cl- channel blockers have effects on other ion channels. Most notably, Cl- channel blockers such as the fenamates (e.g. niflumic acid and flufenamic acid) activate Ca2+-dependent K+ channels, although other pharmacological overlaps have been discovered. In this article, we highlight the complex pharmacology of Ca2+-activated Cl- channels and the caveats associated with using these blockers--a necessary requirement because many researchers use Cl- channel blockers as probes for Cl- channel activity. Moreover, we discuss the argument for a common structural motif between Ca2+-activated Cl- channels and Ca2+-dependent K+ channels, which has led to the possibility that the molecular identity of Cl- channels will be revealed by research in this new direction, in addition to the use of existing candidates such as the CLCA, Bestrophin and tweety genes." @default.
• W2076271650 created "2016-06-24" @default.
• W2076271650 creator A5018843667 @default.
• W2076271650 creator A5078907845 @default.
• W2076271650 date "2007-01-01" @default.
• W2076271650 modified "2023-10-18" @default.
• W2076271650 title "Overlapping pharmacology of Ca2+-activated Cl− and K+ channels" @default.
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• W2076271650 doi "https://doi.org/10.1016/j.tips.2006.11.004" @default.
• W2076271650 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17150263" @default.
• W2076271650 hasPublicationYear "2007" @default.
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