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New progesterone receptor antagonists: 3,3-disubstituted-5-aryloxindoles
Andrew Fensome1, Reinhold Bender, Jeffrey Cohen
1Chemical Sciences, Wyeth Research, Collegeville, PA 19426, USA. fensoma@wyeth.com
Bioorganic & Medicinal Chemistry Letters
|November 7, 2002
Abstract:
A new series of 3,3-disubstituted-5-aryloxindoles has been synthesized and evaluated for progesterone receptor antagonist (PR) activity in a T47D cell alkaline phosphatase assay and for their ability to bind PR in competition binding studies. In this communication, the synthesis and structure-activity relationships (SARs) of various 3,3-substituents are discussed where it is clear that small alkyl and spiroalkyl groups are required to achieve better PR antagonist activity.