Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1395209 | European Journal of Medicinal Chemistry | 2009 | 6 Pages |
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 IC50 value of 0.086 μM, suggesting that further development of such compounds may be of interest.
Graphical abstractA series of alkylidenethiosemicarbazide compounds were synthesized and their inhibitory activities against the diphenolase activity of mushroom tyrosinase were investigated. Compound 1f was found to be the best potent compound with IC50 value of 0.086 μM.Figure optionsDownload full-size imageDownload as PowerPoint slide