ACS Medicinal Chemistry Letters · 2011 · 160 citations · 9 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryMolecular PharmacologyHedgehog SignalingHit-to-lead OptimizationLead Compound DesignLead DiscoveryPotency OptimizationCanonical Hedgehog SignalingDiscoveryHedgehog Pathway InhibitorsHedgehog Signaling InhibitionPharmacological Targeting Of Hedgehog SignalingStructure-based Lead DiscoveryStructure-based Lead IdentificationStructure-guided Lead Discovery
Inhibitors of the Hedgehog signaling pathway have generated a great deal of interest in the oncology area due to the mounting evidence of their potential to provide promising therapeutic options for patients. Herein, we describe the discovery strategy to overcome the issues inherent in lead structure 1 that resulted in the identification of Smoothened inhibitor 1-((2R,4R)-2-(1H-benzo[d]imidazol-2-yl)-1-methylpiperidin-4-yl)-3-(4-cyanophenyl)urea (PF-04449913, 26), which has been advanced to human clinical studies.
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Inhibition of Hedgehog signaling by direct binding of cyclopamine to Smoothened
James Chen, Jussi Taipale, Michael K. Cooper et al. · Genes & Development · 2002 · 1.5K citations · Full text
Effects of oncogenic mutations in Smoothened and Patched can be reversed by cyclopamine
Jussi Taipale, James Chen, Michael K. Cooper et al. · Nature · 2000 · 1.3K citations
R. Scott Obach · Drug Metabolism and Disposition · 1999 · 1.2K citations
Small molecule modulation of Smoothened activity
James Chen, Jussi Taipale, Keith E. Young et al. · Proceedings of the National Academy of Sciences · 2002 · 996 citations