Discovery of a Potent and Orally Active Hedgehog Pathway Antagonist (IPI-926)

Martin Tremblay(Infinity Pharmaceuticals (United States)), André Lescarbeau(Infinity Pharmaceuticals (United States)), Michael J. Grogan(Infinity Pharmaceuticals (United States)), Eddy Tan(Infinity Pharmaceuticals (United States)), Grace Lin(Infinity Pharmaceuticals (United States)), Brian C. Austad(Infinity Pharmaceuticals (United States)), Lin-Chen Yu(Infinity Pharmaceuticals (United States)), Mark L. Behnke(Infinity Pharmaceuticals (United States)), Somarajan Nair(Infinity Pharmaceuticals (United States)), Margit Hagel(Infinity Pharmaceuticals (United States)), Kerry White(Infinity Pharmaceuticals (United States)), James Conley(Infinity Pharmaceuticals (United States)), Joseph Manna(Infinity Pharmaceuticals (United States)), Teresa M. Alvarez-Diez(Infinity Pharmaceuticals (United States)), Jennifer Hoyt(Infinity Pharmaceuticals (United States)), Caroline Woodward(Infinity Pharmaceuticals (United States)), Jens Sydor(Infinity Pharmaceuticals (United States)), Melissa Pink(Infinity Pharmaceuticals (United States)), John R. MacDougall(Infinity Pharmaceuticals (United States)), Matthew Campbell(Infinity Pharmaceuticals (United States)), Jill Cushing(Infinity Pharmaceuticals (United States)), Jeanne A. Ferguson(Infinity Pharmaceuticals (United States)), Michael S. Curtis(Infinity Pharmaceuticals (United States)), Karen McGovern(Infinity Pharmaceuticals (United States)), Margaret Read(Infinity Pharmaceuticals (United States)), Vito J. Palombella(Infinity Pharmaceuticals (United States)), Julian Adams(Infinity Pharmaceuticals (United States)), Alfredo Castro(Infinity Pharmaceuticals (United States))
Journal of Medicinal Chemistry
June 12, 2009
Cited by 251Open Access
Full Text

Abstract

Recent evidence suggests that blocking aberrant hedgehog pathway signaling may be a promising therapeutic strategy for the treatment of several types of cancer. Cyclopamine, a plant Veratrum alkaloid, is a natural product antagonist of the hedgehog pathway. In a previous report, a seven-membered D-ring semisynthetic analogue of cyclopamine, IPI-269609 (2), was shown to have greater acid stability and better aqueous solubility compared to cyclopamine. Further modifications of the A-ring system generated three series of analogues with improved potency and/or solubility. Lead compounds from each series were characterized in vitro and evaluated in vivo for biological activity and pharmacokinetic properties. These studies led to the discovery of IPI-926 (compound 28), a novel semisynthetic cyclopamine analogue with substantially improved pharmaceutical properties and potency and a favorable pharmacokinetic profile relative to cyclopamine and compound 2. As a result, complete tumor regression was observed in a Hh-dependent medulloblastoma allograft model after daily oral administration of 40 mg/kg of compound 28.


Related Papers