Biology-oriented synthesis of a withanolide-inspired compound collection reveals novel modulators of hedgehog signaling

Angew Chem Int Ed Engl. 2015 May 4;54(19):5596-602. doi: 10.1002/anie.201500112. Epub 2015 Mar 3.

Abstract

Biology-oriented synthesis employs the structural information encoded in complex natural products to guide the synthesis of compound collections enriched in bioactivity. The trans-hydrindane dehydro-δ-lactone motif defines the characteristic scaffold of the steroid-like withanolides, a plant-derived natural product class with a diverse pattern of bioactivity. A withanolide-inspired compound collection was synthesized by making use of three key intermediates that contain this characteristic framework derivatized with different reactive functional groups. Biological evaluation of the compound collection in cell-based assays that monitored biological signal-transduction processes revealed a novel class of Hedgehog signaling inhibitors that target the protein Smoothened.

Keywords: biology-oriented synthesis; chemical biology; hedgehog pathway; natural products; total synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Products / chemical synthesis
  • Biological Products / chemistry
  • Biological Products / pharmacology*
  • Dose-Response Relationship, Drug
  • Hedgehogs / metabolism*
  • Molecular Conformation
  • Signal Transduction / drug effects*
  • Structure-Activity Relationship
  • Withanolides / chemical synthesis
  • Withanolides / chemistry
  • Withanolides / pharmacology*

Substances

  • Biological Products
  • Withanolides