Five pimarane diterpenoids from Kaempferia champasakensis and their cytotoxic activities

被引:0
|
作者
Do, Kiep Minh [1 ]
Hoshino, Shotaro [2 ]
Kodama, Takeshi [1 ]
Nguyen, Hien Minh [3 ]
Ikumi, Naotaka [4 ]
Onaka, Hiroyasu [2 ]
Morita, Hiroyuki [1 ]
机构
[1] Univ Toyama, Inst Nat Med, 2630 Sugitani, Toyama 9300194, Japan
[2] Gakushuin Univ, Fac Sci, 1-5-1 Mejiro,Toshima Ku, Tokyo 1718588, Japan
[3] Ton Duc Thang Univ, Fac Pharm, Ho Chi Minh City 700000, Vietnam
[4] Japan Prevent Med Lab Co Ltd, 3-6-36 Toyoda,Suruga Ku, Shizuoka 4228027, Japan
关键词
Kaempferia champasakensis; Isopimarane; Kaempferiols E-I; Cytotoxicity;
D O I
10.1007/s11418-024-01829-8
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A phytochemical investigation of Kaempferia champasakensis rhizomes led to the isolation of five new pimarane diterpenes, kaempferiols E-I (1-5). The structures of 1-5 were elucidated by extensive spectroscopic techniques, including HR-ESI-MS, UV, IR, and 1D and 2D NMR. The absolute configurations of 1-3 were determined by the modified Mosher method, and those of 4 and 5 were established by ECD calculations. Further cytotoxic assay for all isolated compounds against three human cancer cell lines, lung cancer (A549), cervical cancer (HeLa), and breast cancer (MCF-7) indicated that 5 showed moderate cytotoxic activities against the three tested cell lines, with IC50 values of 44.78, 25.97, and 41.39 M mu for A549, HeLa, and MCF-7 cell lines, respectively.
引用
收藏
页码:908 / 918
页数:11
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