†School of Pharmacy, University of Nottingham Malaysia Campus, Jalan Broga, 43500 Semenyih, Selangor, Malaysia.
‡School of Pharmacy, Centre for Biomolecular Sciences, The University of Nottingham, University Park, Nottingham, Nottinghamshire NG72RD, U.K.
J Nat Prod. 2015 May 22;78(5):1129-38. doi: 10.1021/acs.jnatprod.5b00117. Epub 2015 Apr 28.
Six new indole alkaloids, viz., cononusine (1, a rare example of an iboga-pyrrolidone conjugate), ervaluteine (2), vincamajicine (3), tacamonidine (4), 6-oxoibogaine (5), and N(4)-chloromethylnorfluorocurarine chloride (6), and two new vobasinyl-iboga bisindole alkaloids, ervatensines A (7) and B (8), in addition to other known alkaloids, were isolated from the stem-bark extract of the Malayan Tabernaemontana corymbosa. The structures of these alkaloids were established on the basis of NMR and MS analyses and, in one instance (7), confirmed by X-ray diffraction analysis. Vincamajicine (3) showed appreciable activity in reversing multidrug resistance in vincristine-resistant KB cells (IC50 2.62 μM), while ervatensines A (7) and B (8) and two other known bisindoles displayed pronounced in vitro growth inhibitory activity against human KB cells (IC50 < 2 μM). Compounds 7 and 8 also showed good growth inhibitory activity against A549, MCF-7, MDA-468, HCT-116, and HT-29 cells (IC50 0.70-4.19 μM). Cell cycle and annexin V-FITC apoptosis assays indicated that compounds 7 and 8 inhibited proliferation of HCT-116 and MDA-468 cells, evoking apoptotic and necrotic cell death.
从马来亚 Tabernaemontana corymbosa 的茎皮提取物中分离得到了六个新的吲哚生物碱,即 cononusine(1,iboga-pyrrolidone 共轭物的罕见实例)、ervaluteine(2)、vincamajicine(3)、tacamonidine(4)、6-oxoibogaine(5)和 N(4)-chloromethylnorfluorocurarine chloride(6),以及两个新的 vobasinyl-iboga 双吲哚生物碱 ervatensines A(7)和 B(8),此外还有其他已知的生物碱。这些生物碱的结构是基于 NMR 和 MS 分析确定的,在一种情况下(7),通过 X 射线衍射分析得到了证实。Vincamajicine(3)在逆转长春新碱耐药 KB 细胞的多药耐药性方面表现出相当大的活性(IC50 为 2.62 μM),而 ervatensines A(7)和 B(8)以及另外两个已知的双吲哚则显示出对人 KB 细胞的显著体外生长抑制活性(IC50 < 2 μM)。化合物 7 和 8 对 A549、MCF-7、MDA-468、HCT-116 和 HT-29 细胞也表现出良好的生长抑制活性(IC50 为 0.70-4.19 μM)。细胞周期和 annexin V-FITC 凋亡分析表明,化合物 7 和 8 抑制了 HCT-116 和 MDA-468 细胞的增殖,引发了凋亡和坏死性细胞死亡。