A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds

Eur J Med Chem. 2009 Apr;44(4):1773-8. doi: 10.1016/j.ejmech.2008.04.002. Epub 2008 Apr 27.

Abstract

A series of alkylidenethiosemicarbazide compounds were synthesized and their inhibitory effects on the diphenolase activity of mushroom tyrosinase were evaluated. The results showed that most of the synthesized compounds exhibited significant inhibitory activities. Especially, compound 1f was found to be the most potent inhibitor with IC(50) value of 0.086 microM, suggesting that further development of such compounds may be of interest.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Agaricales / enzymology
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / pharmacology*
  • Inhibitory Concentration 50
  • Monophenol Monooxygenase / antagonists & inhibitors*
  • Semicarbazides / chemical synthesis
  • Semicarbazides / chemistry*
  • Semicarbazides / pharmacology*

Substances

  • Enzyme Inhibitors
  • Semicarbazides
  • carbamylhydrazine
  • Monophenol Monooxygenase