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Bioorg Med Chem Lett ; 24(5): 1269-73, 2014 Mar 01.
Article in English | MEDLINE | ID: mdl-24513046

ABSTRACT

A series of lactam sulfonamides has been discovered and optimized as inhibitors of the Kv1.5 potassium ion channel for treatment of atrial fibrillation. In vitro structure-activity relationships from lead structure C to optimized structure 3y are described. Compound 3y was evaluated in a rabbit PD-model and was found to selectively prolong the atrial effective refractory period at submicromolar concentrations.


Subject(s)
Kv1.5 Potassium Channel/antagonists & inhibitors , Lactams/chemistry , Potassium Channel Blockers/chemistry , Pyrrolidinones/chemistry , Sulfonamides/chemistry , Animals , Dogs , Half-Life , Humans , Kv1.5 Potassium Channel/metabolism , Potassium Channel Blockers/chemical synthesis , Potassium Channel Blockers/pharmacokinetics , Pyrrolidinones/chemical synthesis , Pyrrolidinones/pharmacokinetics , Rabbits , Rats , Structure-Activity Relationship , Sulfonamides/chemical synthesis , Sulfonamides/pharmacokinetics
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