Revealing the Pharmacophore of Ipomoeassin F through Molecular Editing

Org Lett. 2016 Apr 1;18(7):1674-7. doi: 10.1021/acs.orglett.6b00555. Epub 2016 Mar 21.

Abstract

Ipomoeassin F, the flagship congener of a resin glycoside family exhibited single-digit nanomolar IC50 values against several cancer cell lines. To facilitate drug discovery based on this unique yet underexplored natural product, we performed the most sophisticated SAR studies of ipomoeassin F to date, which not only greatly bettered our understanding of its pharmacophore but also led to the discovery of two new derivatives (3 and 27) with similar potency but improved synthetic profile. The work presented here opens new avenues toward harnessing the medicinal potential of the ipomoeassin family of glycolipids in the future.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry
  • Biological Products
  • Cell Line, Tumor
  • Drug Discovery
  • Drug Screening Assays, Antitumor
  • Glycoconjugates / chemical synthesis*
  • Glycoconjugates / chemistry
  • Glycoconjugates / pharmacology*
  • Humans
  • Inhibitory Concentration 50
  • Molecular Structure

Substances

  • Antineoplastic Agents
  • Biological Products
  • Glycoconjugates
  • ipomoeassin F