Novel vitamin E derivative with 4-substituted resorcinol moiety has both antioxidant and tyrosinase inhibitory properties |
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Authors: | Kuniyoshi Shimizu Ryuichiro Kondo Kokki Sakai Norio Takeda Tetsuji Nagahata Takayuki Oniki |
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Affiliation: | (1) Kansai Koso Co. Ltd., 816-0921 Ohnojo, Japan;(2) Kyushu Dental College, 803-8580 Kitakyushu, Japan;(3) Laboratory of Forest Chemistry and Biochemistry, Department of Forest Products, Faculty of Agriculture, Kyushu University Graduate School, 6-10-1 Hakozaki, Higashiku, 812-8581 Fukuoka, Japan |
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Abstract: | A novel vitamin E derivative, (6″-hydroxy-2″,5″,7″,8″-tetramethylchroman-2″-yl) methyl 3-(2′,4′-dihydroxyphenyl)propionate (TM4R), which has a chromanoxyl ring and 4-substituted resorcinol moieties, was synthesized; and its inhibitory effects on tyrosinase, antioxidant ability, and lightening effect of ultraviolet B (UVB)-induced hyperpigmentation were estimated. TM4R showed potent inhibitory activity on tyrosinase, which is the rate-limiting enzyme in melanogenesis. The scavenging activities of TM4R on 1,1-diphenyl-2-picrylhydrazyl and hydroxyl radicals were found to be nearly the same as those of α-tocopherol. Furthermore, an efficient lightening effect was observed following topical application of TM4R to UVB-stimulated hyperpigmented dorsal skin of brownish guinea pigs. These results suggest that TM4R may be a candidate for an efficient whitening agent, possibly by inhibiting tyrosinase activity and biological reactions caused by reactive oxygen species. |
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