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Corrigendum to “A newly synthesized, potent tyrosinase inhibitor: 5-(6-Hydroxy-2-naphthyl)-1,2,3-benzenetriol” [Bioorg. Med. Chem. Lett. 20 (2010) 4882–4884]

✍ Scribed by Jehun Choi; Sung Jin Bae; Young Mi Ha; Jae Kyung No; Eun Kyeong Lee; Jun Sik Lee; Suhee Song; Hyojin Lee; Hongsuk Suh; Byung Pal Yu; Hae Young Chung

Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 139 KB
Volume: 21
Category: Article
ISSN: 0960-894X
DOI: 10.1016/j.bmcl.2010.10.049

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✦ Synopsis

The authors regret that this article contains one error. The structure of Kojic acid (4) was revised. Therefore, the following correction should be made.

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A newly synthesized, potent tyrosinase i

A newly synthesized, potent tyrosinase inhibitor: 5-(6-Hydroxy-2-naphthyl)-1,2,3-benzenetriol

✍ Jehun Choi; Sung Jin Bae; Young Mi Ha; Jae Kyung No; Eun Kyeong Lee; Jun Sik Lee 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 351 KB

In searching for new agents with a depigmenting effect, we synthesized a derivative of resveratrol, 5-(6-hydroxy-2-naphthyl)-1,2,3-benzenetriol (5HNB) with a potent tyrosinase inhibitory activity. 5HNB inhibited mushroom tyrosinase with an IC 50 value of 2.95 lM, which is more potent than the well-