Isolation, Structure Determination, and Anti-HIV Evaluation of Tigliane-Type Diterpenes and Biflavonoid from Stellera chamaejasme

被引:53
作者
Asada, Yoshihisa [1 ]
Sukemori, Aya [2 ]
Watanabe, Takashi [3 ]
Malla, Kuber J. [4 ]
Yoshikawa, Takafumi [2 ]
Li, Wei [5 ]
Kuang, Xinzhu [5 ]
Koike, Kazuo [5 ]
Chen, Chin-Ho [6 ]
Akiyama, Toshiyuki [7 ]
Qian, Keduo [7 ]
Nakagawa-Goto, Kyoko [7 ]
Morris-Natschke, Susan L. [7 ]
Lu, Yan [7 ]
Lee, Kuo-Hsiung [7 ,8 ]
机构
[1] Tokyo Univ Sci, Fac Pharmaceut Sci, Noda, Chiba 2788510, Japan
[2] Kitasato Univ, Sch Pharmaceut Sci, Minato Ku, Tokyo 1088641, Japan
[3] Kochi Univ Technol, Lab Studying Complementary & Med Resources, Kochi 7828502, Japan
[4] Dept Plant Resources, Kathmandu, Nepal
[5] Toho Univ, Fac Pharmaceut Sci, Funabashi, Chiba 2748510, Japan
[6] Duke Univ, Med Ctr, SORF, Durham, NC 27710 USA
[7] Univ N Carolina, UNC Eshelman Sch Pharm, Nat Prod Res Labs, Chapel Hill, NC 27599 USA
[8] China Med Univ & Hosp, Chinese Med Res & Dev Ctr, Taichung, Taiwan
来源
JOURNAL OF NATURAL PRODUCTS | 2013年 / 76卷 / 05期
关键词
ESTERS;
D O I
10.1021/np300815t
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Five novel tigliane-type diterpenes, stelleracins A-E (3-7), a novel flavanone dimer, chamaeflavone A (8), and six known compounds were isolated from the roots of Stellera chamaejasme. Their structures were elucidated by extensive spectroscopic analyses. The isolated compounds were evaluated for anti-HIV activity in MT4 cells. New compounds 3-5 showed potent anti-HIV activity (EC90 0.00056-0.0068 mu M) and relatively low or no cytotoxicity (IC50 4.4-17.2 mu M). These new compounds represent promising new leads for development into anti-AIDS clinical trial candidates.
引用
收藏
页码:852 / 857
页数:6
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