Isolation of tyrosinase and melanogenesis inhibitory flavonoids from Juniperus chinensis fruits

被引:18
作者
Park, Sang-a [1 ]
Jegal, Jonghwan [1 ]
Chung, Ki Wung [1 ]
Jung, Hee Jin [1 ]
Noh, Sang Gyun [1 ]
Chung, Hae Young [1 ]
Ahn, Jongmin [2 ,3 ]
Kim, Jinwoong [2 ,3 ]
Yang, Min Hye [1 ]
机构
[1] Pusan Natl Univ, Coll Pharm, Busan, South Korea
[2] Seoul Natl Univ, Coll Pharm, Seoul, South Korea
[3] Seoul Natl Univ, Res Inst Pharmaceut Sci, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Juniperus chinensis fruit; amentoflavone-7-O-beta-D-glucoside; quercetin-7-O-alpha-L-rhamnoside; tyrosinase; melanogenesis; COMMUNIS VAR. DEPRESSA; SKIN PIGMENTATION; GLYCOSIDES; CONSTITUENTS; BIFLAVONOIDS; BERRIES; EXTRACT;
D O I
10.1080/09168451.2018.1511367
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A new biflavonoid, amentoflavone-7-O-ss-D-glucoside, and thirteen known flavonoids were isolated from the fruits of Juniperus chinensis using a bioactivity-guided method and their tyrosinase inhibitory effects were tested using a mushroom tyrosinase bioassay. Two isolates, hypolaetin-7-O-ss-D-glucoside and quercetin-7-O-alpha-L-rhamnoside, were found to reduce tyrosinase activity at a concentration of 50 mu M. Quercetin-7-O-alpha-L-rhamnoside attenuated cellular tyrosinase activity and melanogenesis in alpha-MSH plus IBMX-stimulated B16F10 melanoma cells. Molecular docking simulation revealed that quercetin-7-O-alpha-L-rhamnoside inhibits tyrosinase activity by hydrogen bonding with residues His85, His244, Thr261, and Gly281 of tyrosinase.
引用
收藏
页码:2041 / 2048
页数:8
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