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The biological activities of cardenolide triglycosides from stems, twigs, and leaves of Nerium oleander
Authors:Yuhua Bai  Ming Zhao  Liming Bai  Ryo Hasegawa  Jun-ichi Sakai  Toshiaki Hasegawa  Tomokazu Mitsui  Hirotsugu Ogura  Takao Kataoka  Katsutoshi Hirose  Masayoshi Ando
Institution:1. Department of Pharmacy, Daqing Campus of Harbin Medical University, Daqing Hi-Tech Development Zone, Xinyang Road, Daqing, 163319, China
2. College of Chemistry and Chemistry Engineering, Qiqihar University, Qiqihar, 161006, China
3. Graduate School of Science and Technology, Niigata University, Niigata, 950-2181, Japan
4. Department of Chemistry and Chemical Engineering, Niigata University, Niigata, 950-2181, Japan
5. Niigata Research Laboratory, Mitsubishi Gas Chemical Company, Inc., Niigata, 950-3112, Japan
6. Center for Biological Resources and Informatics, Tokyo Institute of Technology, Yokohama, 226-8501, Japan
7. KNC Laboratories Co. Ltd., Kobe, 651-2271, Japan
Abstract:Sixteen cardenolide triglycosides (1?C16) were isolated from stems, twigs, and leaves of Nerium oleander. Among them, 3??-O-(4-O-gentiobiosyl-d-diginosyl)-7??,8-epoxy-14-hydroxy-5??,14??-card-20(22)-enolide, named cardenolide B-3 (16), was isolated from natural sources for the first time. The in vitro anti-inflammatory activities of compounds 1?C16 were examined on the basis of inhibitory activity against the induction of intercellular adhesion molecule-1 (ICAM-1). Compounds 1?C5 were active at an IC50 value of less than 7 ??M. The cytotoxic activity of isolated compounds was evaluated against three human cell lines: normal human fibroblast cells (W-38), malignant tumor cells induced from WI-38 (VA-13), and human liver tumor cells (HepG2). Compounds 1?C5 were active toward WI-38 cells; compounds 1, 3, and 5 were active toward VA-13 cells; and compounds 1?C5 were active toward HepG2 cells at IC50 values of less than 10 ??M. The multidrug-resistant (MDR) cancer-reversal activity of compounds 1?C16 was evaluated on the basis of the amount of calcein accumulated in MDR human ovarian cancer 2780AD cells in the presence of each compound. Compounds 13 and 14 showed significant effects on calcein accumulation.
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