Synthesis and evaluation of antioxidant phenolic diaryl hydrazones as potent antiangiogenic agents in atherosclerosis

Bioorg Med Chem. 2016 Aug 15;24(16):3571-8. doi: 10.1016/j.bmc.2016.05.067. Epub 2016 May 30.

Abstract

A series of bis-hydrazones derived from diaryl and diaryl ether hydroxybenzaldehyde frames 1 and 2 have been synthesized as potential antioxidant and antiangiogenic agents, two properties required to limit atherogenesis and cardiovascular events. These compounds were evaluated for their ability to neutralize free radical formation, to block endothelial cell-induced low-density lipoprotein oxidation (monitored by the formation of TBARS), an essential step in atherogenesis, and subsequent toxicity, to prevent angiogenesis evoked by low oxidized LDL concentration (monitored by the formation of capillary tubes on Matrigel) and to inhibit intracellular ROS increase involved in the angiogenic signaling. A structure/activity study has been carried out and finally allowed to select the phenolic diaryl ether hydralazine derivative 2a, sharing all these protective properties, as a promising hit for further development.

Keywords: Angiogenesis; Antioxidant; Atherosclerosis; Biphenyl derivatives; Hydrazone; Polyphenol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenesis Inhibitors / chemical synthesis*
  • Angiogenesis Inhibitors / pharmacology*
  • Angiogenesis Inhibitors / therapeutic use
  • Antioxidants / chemical synthesis*
  • Antioxidants / pharmacology*
  • Atherosclerosis / drug therapy*
  • Carbon-13 Magnetic Resonance Spectroscopy
  • Cell Line
  • Humans
  • Hydrazones / chemical synthesis*
  • Hydrazones / pharmacology*
  • Lipoproteins, LDL / metabolism
  • Proton Magnetic Resonance Spectroscopy
  • Reactive Oxygen Species / metabolism
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Angiogenesis Inhibitors
  • Antioxidants
  • Hydrazones
  • Lipoproteins, LDL
  • Reactive Oxygen Species
  • oxidized low density lipoprotein