Synthesis and Activity against Mycobacterium tuberculosis of Olivacine and Oxygenated Derivatives

Molecules. 2018 Jun 9;23(6):1402. doi: 10.3390/molecules23061402.

Abstract

The tetracyclic pyrido[4,3-b]carbazole olivacine and four of its oxygenated derivatives have been synthesized by a late-stage palladium-catalyzed Heck-type cyclization of the pyrrole ring as a key step. In a test for the inhibition of the growth of Mycobacterium tuberculosis, 9-methoxyolivacine showed the most significant inhibitory activity against Mycobacterium tuberculosis, with an MIC90 value of 1.5 μM.

Keywords: catalysis; cyclization; inhibitory activity; olivacine; palladium; pyrido[4,3-b]carbazoles.

MeSH terms

  • Carbon-13 Magnetic Resonance Spectroscopy
  • Crystallography, X-Ray
  • Cyclization
  • Ellipticines / chemical synthesis*
  • Ellipticines / pharmacology*
  • Microbial Sensitivity Tests
  • Mycobacterium tuberculosis / drug effects*
  • Oxygen / chemistry*
  • Proton Magnetic Resonance Spectroscopy
  • Spectrometry, Mass, Electrospray Ionization
  • Spectrophotometry, Ultraviolet

Substances

  • Ellipticines
  • olivacine
  • Oxygen