The hypopigmentary action of KI-063 (a new tyrosinase inhibitor) combined with terrein

Author:

Kim Dong-Seok1,Lee Sangku2,Lee Hyun-Kyung3,Park Seo-Hyoung34,Ryoo In-Ja2,Yoo Ick-Dong2,Kwon Sun-Bang4,Baek Kwang Jin1,Na Jung-Im3,Park Kyoung-Chan3

Affiliation:

1. Department of Biochemistry, College of Medicine, Chung-Ang University, 221 Heukseok-Dong Dongjak-Gu, Seoul 156-756, Republic of Korea

2. National Cosmeceutical Research Center, Korea Research Institute of Bioscience and Biotechnology, 52 Oeun-Dong, Yuseong-Gu, Daejeon 305-333, Korea

3. Department of Dermatology, Seoul National University College of Medicine, 28 Yongon-Dong, Chongno-Gu, Seoul 110-744, Republic of Korea

4. Welskin Co. Ltd, 28 Yongon-Dong, Chongno-Gu, Seoul 110-744, Korea

Abstract

Abstract Resorcinol derivatives are known to inhibit melanin synthesis. In this study, resorcinol derivatives were synthesized and screened for their activity on melanogenesis. KI-063 (a tyrosinase inhibitor) was examined for its effects on melanogenesis using a spontaneously immortalized mouse melanocyte cell line (Mel-Ab). In a cell-free system, KI-063 directly inhibited tyrosinase, the rate-limiting melanogenic enzyme. Moreover, in a cell system, it inhibited melanin synthesis in a concentration-dependent manner. In addition, KI-063 inhibited the activity of cellular tyrosinase. Thus, this study examined the effects of a combination of KI-063 with terrein, an agent that down-regulates microphthalmia-associated transcription factor. The data suggest that KI-063 has an additive effect in combination with terrein. Thus, the suppression of tyrosinase activity by KI-063 and the inhibition of tyrosinase production by terrein appear to be an optimal combination for skin whitening.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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