N-Benzylbenzamides: A new class of potent tyrosinase inhibitors

A series of potent inhibitors of tyrosinase and their structure–activity relationships are described. N-Benzylbenzamide derivatives (1–21) with hydroxyl(s) were synthesized and tested for their tyrosinase inhibitory activity. With this series, compound 15 provided a potent tyrosinase inhibition: it...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2006-05, Vol.16 (10), p.2682-2684
Hauptverfasser: Cho, Sung Jin, Roh, Jung Seop, Sun, Won Suck, Kim, Sung Han, Park, Ki Duk
Format: Artikel
Sprache:eng
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Zusammenfassung:A series of potent inhibitors of tyrosinase and their structure–activity relationships are described. N-Benzylbenzamide derivatives (1–21) with hydroxyl(s) were synthesized and tested for their tyrosinase inhibitory activity. With this series, compound 15 provided a potent tyrosinase inhibition: it effectively inhibited the oxidation of l-DOPA catalyzed by mushroom tyrosinase with IC50 of 2.2μM. A series of potent inhibitors of tyrosinase and their structure–activity relationships are described. N-Benzylbenzamide derivatives (1–21) with hydroxyl(s) were synthesized and tested for their tyrosinase inhibitory activity. With this series, compound 15 provided a potent tyrosinase inhibition: it effectively inhibited the oxidation of l-DOPA catalyzed by mushroom tyrosinase with an IC50 of 2.2μM.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2006.02.018