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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.
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页码:2041 / 2048
页数:8
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