Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1378039 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
Mifepristone is a non-selective antagonist of 3-oxosteroid receptors with both abortifacient and anti-diabetic activities. For glucocorticoid receptor (GR) program, we sought an unexplored, synthetically accessible phosphorus-containing steroidal mimetic of mifepristone, suitable for parallel synthesis of analogues. One compound 4a, with high oral bioavailability (59%) in rat, exhibited functional antagonism of GR in oral glucose tolerance test (OGTT). Thus this series of compounds might be potentially useful for the treatment of type II diabetes.
Graphical abstractThe synthesis and biological activities of the glucocorticoid receptor antagonists 4 and 5 are reported.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Weiqin Jiang, James J. Fiordeliso, George Allan, Olivia Linton, Pamela Tannenbaum, Jun Xu, Peifang Zhu, Joseph Gunnet, Keith Demarest, Scott Lundeen, Zhihua Sui,