Discovery of Novel Cinchona-Alkaloid-Inspired Oxazatwistane Autophagy Inhibitors

Angew Chem Int Ed Engl. 2017 Feb 13;56(8):2145-2150. doi: 10.1002/anie.201611670. Epub 2017 Jan 18.

Abstract

The cinchona alkaloids are a privileged class of natural products and are endowed with diverse bioactivities. However, for compounds with the closely-related oxazatricyclo[4.4.0.0]decane ("oxazatwistane") scaffold, which are accessible from cinchonidine and quinidine by means of ring distortion and modification, biological activity has not been identified. We report the synthesis of an oxazatwistane compound collection through employing state-of-the-art C-H functionalization, and metal-catalyzed cross-coupling reactions as key late diversity-generating steps. Exploration of oxazatwistane bioactivity in phenotypic assays monitoring different cellular processes revealed a novel class of autophagy inhibitors termed oxautins, which, in contrast to the guiding natural products, selectively inhibit autophagy by inhibiting both autophagosome biogenesis and autophagosome maturation.

Keywords: alkaloids; autophagy; inhibitors; medicinal chemistry; natural products.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagy / drug effects*
  • Biological Products / chemical synthesis
  • Biological Products / chemistry
  • Biological Products / pharmacology
  • Cinchona / chemistry
  • Cinchona Alkaloids / chemical synthesis
  • Cinchona Alkaloids / chemistry*
  • Cinchona Alkaloids / pharmacology*
  • HEK293 Cells
  • Humans
  • MCF-7 Cells

Substances

  • Biological Products
  • Cinchona Alkaloids