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SK3 is an important component of K(+) channels mediating the afterhyperpolarization in cultured rat SCG neurones.

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Compounds that block both intermediate-conductance (IK(Ca)) and small-conductance (SK(Ca)) calcium-activated potassium channels.

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Journal of medicinal chemistry·2000

Differences in the actions of some blockers of the calcium-activated potassium permeability in mammalian red cells.

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On the concept of a bivalent pharmacophore for SKCa channel blockers: synthesis, pharmacological testing, and radioligand binding studies on mono-, bis-, and tris-quinolinium compounds.

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Fine-Grained Structural Classification of Biosynthetic Gene Cluster-Encoded Products.

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Classification and properties of peripheral adrenergic receptors

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Synthesis and structure-activity relationships of cetiedil analogues as blockers of the Ca(2+)-activated K+ permeability of erythrocytes.

SK3 is an important component of K(+) channels mediating the afterhyperpolarization in cultured rat SCG neurones.

Compounds that block both intermediate-conductance (IK(Ca)) and small-conductance (SK(Ca)) calcium-activated potassium channels.

Synthesis, molecular modeling, and pharmacological testing of bis-quinolinium cyclophanes: potent, non-peptidic blockers of the apamin-sensitive Ca(2+)-activated K(+) channel.

Differences in the actions of some blockers of the calcium-activated potassium permeability in mammalian red cells.

On the concept of a bivalent pharmacophore for SKCa channel blockers: synthesis, pharmacological testing, and radioligand binding studies on mono-, bis-, and tris-quinolinium compounds.

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