Two new indole alkaloids from Tabernaemontana contorta Stapf

被引:7
|
作者
Melacheu, Gertrude Laura Foudjo [1 ]
Njoya, Emmanuel Mfotie [2 ,3 ]
Jouda, Jean-Bosco [1 ]
Kweka, Brussine Nadege Wakeu [1 ]
Mbazoa, Celine Djama [1 ]
Wang, Fei [2 ]
Wandji, Jean [1 ]
机构
[1] Univ Yaounde I, Fac Sci, Dept Organ Chem, POB 812, Yaounde, Cameroon
[2] Chinese Acad Sci, Chengdu Inst Biol, Key Lab Nat Med & Clin Translat, Chengdu, Sichuan, Peoples R China
[3] Univ Yaounde I, Fac Sci, Dept Biochem, POB 812, Yaounde, Cameroon
关键词
Tabernaemontana contorta; Indole alkaloids; NO production; Cell proliferation; IN-VITRO; CATHARINENSIS; TRITERPENOIDS;
D O I
10.1016/j.phytol.2019.01.028
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Two new indole alkaloid derivatives, 5,6-dioxo-11-methoxy voacangine (1) and (-)-apparicin-21-one (2), together with four known compounds, voacangine (3), ursolic acid (4), 3-methoxyursolic acid (5) and asiatic acid (6) were isolated from the fruits of Tabernaemontana contorta Stapf (Apocynaceae). Their structures were determined using 1D and 2D NMR and HRESI-MS measurements. The new indole alkaloids were tested on lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophage cells to determine their inhibitory effect on nitric oxide (NO) production, but did not have any significant inhibitory activity. Compound (1) slightly increased the proliferation of RAW 264.7 cells in relation with the increased level of NO released by these cells.
引用
收藏
页码:116 / 119
页数:4
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