Furoquinolines and dihydrooxazole alkaloids with cytotoxic activity from the stem bark of Araliopsis soyauxii

被引:30
|
作者
Nganou, Blaise Kemajou [1 ]
Mbaveng, Armelle T. [2 ,3 ]
Fobofou, Serge A. T. [1 ,4 ,5 ]
Fankam, Aime G. [3 ]
Bitchagno, Gabin Thierry M. [1 ]
Mpetga, James D. Simo [1 ]
Wessjohann, Ludger A. [4 ]
Kuete, Victor [2 ,3 ]
Efferth, Thomas [2 ]
Tane, Pierre [1 ]
机构
[1] Univ Dschang, Dept Chem, POB 67, Dschang, Cameroon
[2] Johannes Gutenberg Univ Mainz, Dept Pharmaceut Biol, Inst Pharm & Biochem, Staudinger Weg 5, D-55128 Mainz, Germany
[3] Univ Dschang, Dept Biochem, POB 67, Dschang, Cameroon
[4] Leibniz Inst Plant Biochem, Dept Bioorgan Chem, Weinberg 3, D-06120 Halle, Saale, Germany
[5] Martin Luther Univ Halle Wittenberg, Inst Pharm, Wolfgang Langenbeck Str 4, D-06120 Halle, Saale, Germany
关键词
Araliopsis soyauxii; Rutaceae; Maculine B; Kokusaginine B; Veprisazole; Cytotoxicity; MULTIDRUG-RESISTANCE; BREAST-CANCER; MODES; TRANSPORTER; RUTACEAE;
D O I
10.1016/j.fitote.2019.01.003
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Two new furoquinoline alkaloids, maculine B (1) and kokusaginine B (2) and one new dihydrooxazole alkaloid, veprisazole (3), along with four known compounds namely, N-13-methyl-3-methoxyrutaecarpine (4), finder-siamine (5), skimmianine (6) and tilianin (7) were isolated from the methanol extract of the stem bark of Araliopsis soyauxii Engl. by various chromatographic methods. Their structures were determined using spectrometry and spectroscopic techniques including NMR and MS. The cytotoxicity of the new compounds compared to that of doxorubicin, the reference anticancer compound, was determined on a panel of nine cancer cell lines including sensitive and drug resistant phenotypes. The three previously undescribed alkaloids displayed selective activities. Maculine B (1), the most active one among the newly described compounds, exhibited IC50 below 30 mu m against CCRF-CEM leukemia and U87MG glioblastoma cells.
引用
收藏
页码:193 / 199
页数:7
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