Tyrosinase inhibitors from the leaves of Eucalyptus globulus

被引:5
|
作者
Lin, Qiao-Mei [1 ]
Wang, Yong [1 ]
Yu, Jin-Hai [2 ]
Liu, Yun-Lai [1 ]
Wu, Xue [1 ]
He, Xiao-Ru [3 ]
Zhou, Zhi-Wang [1 ]
机构
[1] Nanchang Univ, Sch Pharm, Nanchang 330006, Jiangxi, Peoples R China
[2] Univ Jinan, Sch Biol Sci & Technol, Jinan 250022, Shandong, Peoples R China
[3] Jiangxi Univ TCM, Key Lab Modern Preparat TCM, Minist Educ, Nanchang 330004, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Eucalyptus globulus; Eucalyptus; Isoiphionane; Phloroglucinol; Tyrosinase inhibitors; FORMYL-PHLOROGLUCINOL MEROTERPENOIDS; NUCLEAR-MAGNETIC-RESONANCE; ABSOLUTE-CONFIGURATIONS; A-C; CONSTITUENTS; SESQUITERPENOIDS; MACROCARPALS; ASSIGNMENT; GLYCOSIDES; FRUITS;
D O I
10.1016/j.fitote.2019.104418
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new isoiphionane sesquiterpene, named (3S, 5S, 7S, 10R)-3, 11-dihydroxyisoiphion-4-one (1), two new phloroglucinol glycosides, named eucalglobuside A (2) and eucalglobuside B (3), along with 15 known compounds were isolated from the leaves of Eucalyptus globulus. Their structures were elucidated based on extensive spectroscopic analysis and in comparison with literature data. The absolute configuration of compound 1 was determined by ECD calculation. All isolates were evaluated their inhibitory activities against the mushroom tyrosinase. As a result, three sesquiterpenoids, 1, 5 beta, 11-dihydroxy-iphionan-4-one (5), and (-)-globulol (8), exhibited the most potent activities with IC50 values of 14.17 mu M, 10.08 mu M and 9.79 mu M, respectively.
引用
收藏
页数:5
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