Planta Med 2000; 66(1): 11-15
DOI: 10.1055/s-2000-11113
Original Paper
Georg Thieme Verlag Stuttgart · New York

Inhibition of Tyrosinase by Flavonoids, Stilbenes and Related 4-Substituted Resorcinols: Structure-Activity Investigations

Kuniyoshi Shimizu, Ryuichiro Kondo*, and, Kokki Sakai
  • Department of Forest Products, Faculty of Agriculture, Kyushu University, Fukuoka, Japan
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
31. Dezember 2000 (online)

Abstract

Several flavonoids, stilbenes and related 4-substituted resorcinols, obtained from Artocarpus incisus and other plants or synthesized, were tested for their inhibitory activity against tyrosinase. The structure-activity relationships suggested that specific natural or synthesized compounds having the 4-substituted resorcinol skeleton have potent tyrosinase inhibitory ability. Kinetic studies have indicated that specific compounds having the 4-substituted resorcinol skeleton exhibit competitive inhibition of the oxidation of DL-β-(3,4-dihydroxyphenyl)alanine (DL-DOPA) by mushroom tyrosinase. These findings could lead to the design and discovery of new tyrosinase inhibitors.

References

Dr. Ryuichiro Kondo

Department of Forest Products

Faculty of Agriculture

Kyushu University

Fukuoka, 812-8581

Japan

eMail: kondo@agr.kyushu-u.ac.jp

Telefon: +81-92-642-2989