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Progress toward the total synthesis of correolide: A potent and selective Kv1.3 potassium ion channel inhibitor

Posted on:2007-09-07Degree:Ph.DType:Thesis
University:University of California, IrvineCandidate:Roth, Joshua JohnFull Text:PDF
GTID:2448390005962274Subject:Biology
Abstract/Summary:
Correolide, a pentacylic nor-triterpenoid, isolated from Spachea correae is the most potent and selective small molecule inhibitor of the Kv1.3 channel. Selective blockage of the Kv1.3 ion channel results in a series of intracellular events that suppress T-cell proliferation and as a result the immune system. Suppression of T-cell proliferation is an attractive target for immunosuppresive therapies. Studies directed towards the total synthesis of correolide based on two diastereoselective Diels-Alder reactions and an intramolecular Heck reaction are described.
Keywords/Search Tags:Selective, Kv1, Channel
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