Angiogenesis inhibitors derived from thalidomide

Bioorg Med Chem Lett. 2005 Dec 15;15(24):5509-13. doi: 10.1016/j.bmcl.2005.08.086. Epub 2005 Sep 23.

Abstract

5-Hydroxy-2-(2,6-diisopropylphenyl)-1H-isoindole-1,3-dione (5HPP-33: 10), which was obtained during our previous structural development studies on thalidomide, was revealed to possess potent anti-angiogenic activity in a human umbilical vein endothelial cell (HUVEC) assay. Thalidomide (1) and its metabolite, 5-hydroxythalidomide (5-HT: 2), which possesses a hydroxyl group at the position corresponding to that of 5HPP-33, as well as IMiDs (immunomodulatory derivatives of thalidomide: 3 and 5), also showed weak or moderate activity in the same assay.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenesis Inhibitors / chemical synthesis*
  • Angiogenesis Inhibitors / pharmacology
  • Endothelium, Vascular / cytology*
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / physiology
  • Humans
  • Structure-Activity Relationship
  • Thalidomide / analogs & derivatives*
  • Thalidomide / pharmacology*
  • Umbilical Veins

Substances

  • Angiogenesis Inhibitors
  • Thalidomide