Abstract
The voltage-gated potassium channel, Kv1.3, is present in human T-lymphocytes. Blockade of Kv1.3 results in T-cell depolarization, inhibition of T-cell activation, and attenuation of immune responses in vivo. A class of benzamide Kv1.3 channel inhibitors has been identified. The structure-activity relationship within this class of compounds in two functional assays, Rb_Kv and T-cell proliferation, is presented. In in vitro assays, trans isomers display moderate selectivity for binding to Kv1.3 over other Kv1.x channels present in human brain.
MeSH terms
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Benzamides / chemical synthesis*
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Benzamides / pharmacology*
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Brain Chemistry / drug effects
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Cell Division / drug effects
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Humans
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In Vitro Techniques
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Kv1.3 Potassium Channel
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Potassium Channel Blockers / chemical synthesis*
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Potassium Channel Blockers / pharmacology*
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Potassium Channels / drug effects*
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Potassium Channels, Voltage-Gated*
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Rubidium Radioisotopes
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Stereoisomerism
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Structure-Activity Relationship
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T-Lymphocytes / drug effects
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T-Lymphocytes / metabolism
Substances
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Benzamides
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KCNA3 protein, human
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Kv1.3 Potassium Channel
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Potassium Channel Blockers
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Potassium Channels
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Potassium Channels, Voltage-Gated
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Rubidium Radioisotopes