Author/Authors :
Weiqin Jiang، نويسنده , , James J. Fiordeliso، نويسنده , , George Allan، نويسنده , , Olivia Linton، نويسنده , , Pamela Tannenbaum، نويسنده , , Jun Xu، نويسنده , , Peifang Zhu، نويسنده , , Joseph Gunnet، نويسنده , , Keith Demarest، نويسنده , , Scott Lundeen، نويسنده , , Zhihua Sui، نويسنده ,
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.