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 |
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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. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2006.02.018 |