Benzofuran-derived cyclic beta-amino acid scaffold for building a diverse set of flavonoid-like probes and the discovery of a cell motility inhibitor

Org Lett. 2008 Mar 20;10(6):1143-6. doi: 10.1021/ol800050g. Epub 2008 Feb 27.

Abstract

We report here a practical, enantioselective synthesis of benzofuran-derived, cyclic trans-beta-amino acid scaffold. In two cases, tricyclic derivatives having six- and eight-membered unsaturated lactams were obtained from this versatile scaffold. To explore the biological applications, these compounds were subjected to cell-based assays, using NIH3T3 mouse cells to examine their potency as cell motility inhibitors and identified 18 as a potent cell motility inhibitor (IC50 approximately 40 microM in chamber cell migration assay).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids, Cyclic / chemistry*
  • Animals
  • Benzofurans / chemistry*
  • Cell Movement / drug effects*
  • Flavonoids / chemistry*
  • Flavonoids / pharmacology
  • Mice
  • Molecular Probes
  • NIH 3T3 Cells

Substances

  • Amino Acids, Cyclic
  • Benzofurans
  • Flavonoids
  • Molecular Probes
  • benzofuran