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Design, Synthesis, and Characterization of BK Channel Openers Based on Oximation of Abietane Diterpene Derivatives

Overview
Journal Bioorg Med Chem
Specialties Biochemistry
Chemistry
Date 2010 Nov 12
PMID 21067932
Citations 7
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Abstract

Oxime ether derivatives at the benzylic position of unsubstituted, dichloro, trichloro, and monobromo derivatives of the aromatic C-ring of dehydroabietic acid and podocarpic acid were synthesized and evaluated as BK channel openers in an assay system of CHO-K1 cells expressing hBKα channels. Detailed SAR analysis showed that the oximation was particularly effective in the cases of dehydroabietic acid derivatives, and some of these oxime derivatives showed more potent BK channel activities than the standard compound, NS1619. The present studies provide a new structural basis for development of efficient BK channel openers.

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