Synthesis of novel benzo[h]quinolines: wound healing, antibacterial, DNA binding and in vitro antioxidant activity

Eur J Med Chem. 2009 Mar;44(3):981-9. doi: 10.1016/j.ejmech.2008.07.006. Epub 2008 Jul 16.

Abstract

We have characterized a new class of 2-mercapto/2-selenobenzo[h]quinoline-3-carbaldehyde (3/4). Antibacterial potential of these compounds against a wide range of gram-positive and gram-negative bacteria was studied. The selenium containing compound 4 showed significant inhibition zone on Staphylococcus aureus (22.76+/-0.14), Bacillus subtilis (20.63+/-0.24), and Streptococcus pyogenes (19.54+/-0.20) over sulfur containing compound 3. To validate the ethnotherapeutic claims of the synthetic compounds in skin diseases, wound healing activity was studied, besides antioxidant activity to understand the mechanism of wound healing. The interaction behavior of these compounds with DNA was investigated by absorption spectra (obtained K(b) constant for 3 is 2.7x10(5) and for 4 is 3.8x10(6)), viscosity, and thermal denaturation studies. Finally, the results show that the DNA intercalated 3/4 compounds are strong antioxidants; they show significant wound healing activity and protect oxidative DNA damage from harmful free radical reactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / chemical synthesis*
  • Anti-Bacterial Agents / metabolism
  • Anti-Bacterial Agents / pharmacology*
  • Antioxidants / pharmacology*
  • Bacillus subtilis / drug effects
  • DNA / metabolism*
  • Magnetic Resonance Spectroscopy
  • Male
  • Mass Spectrometry
  • Microbial Sensitivity Tests
  • Nucleic Acid Denaturation
  • Quinolines / chemical synthesis*
  • Quinolines / metabolism
  • Quinolines / pharmacology*
  • Rats
  • Rats, Wistar
  • Staphylococcus aureus / drug effects
  • Streptococcus pyogenes / drug effects
  • Wound Healing / drug effects*

Substances

  • Anti-Bacterial Agents
  • Antioxidants
  • Quinolines
  • benzo(h)quinoline
  • DNA