Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1377433 | Bioorganic & Medicinal Chemistry Letters | 2007 | 8 Pages |
Abstract
The design, synthesis, and SAR of a novel series of heterobiaryl phenethanolamine β3 adrenergic receptor agonists are described. The furan analogue 49 was shown to elicit a significant dose-dependent lowering of plasma glucose in a rodent model of type 2 diabetes.
Graphical abstractThe design, synthesis, and SAR of a novel series of heterobiaryl phenethanolamine β3 adrenergic receptor agonists are described. The furan analogue 49 was shown to elicit a significant dose-dependent lowering of plasma glucose in a rodent model of type 2 diabetes.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
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Authors
Barry G. Shearer, Esther Y. Chao, David E. Uehling, David N. Deaton, Conrad Cowan, Bryan W. Sherman, Tula Milliken, Walter Faison, Kathleen Brown, Kimberly K. Adkison, Frank Lee,