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塔柏卡品 A-J,诱导凋亡的吲哚生物碱,来自圆锥山麻杆的叶子。

Tabercarpamines A-J, apoptosis-inducing indole alkaloids from the leaves of Tabernaemontana corymbosa.

机构信息

State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, China Pharmaceutical University , 24 Tong Jia Xiang, Nanjing 210009, People's Republic of China.

出版信息

J Nat Prod. 2014 May 23;77(5):1156-63. doi: 10.1021/np401098y. Epub 2014 Apr 28.

Abstract

A total of 10 new indole alkaloids, tabercarpamines A-J (1-10), were isolated from the leaves of Tabernaemontana corymbosa. Tabercarpamines C-F (3-6) are rare C-14/C-15-seco-tabersonine-type monoterpenoid indole alkaloids, and 5 and 6 are the first examples with a lactone linkage between C-14 and C-20. The structures of these alkaloids were elucidated using spectroscopic methods, and the absolute configurations of 1 and 2 were determined using the ECD exciton chirality method. In addition, an MTT assay was used to examine the growth-inhibitory effects of all new isolates and of two known isolates on MCF-7, HepG2, and SMMC-7721 cells; 1 exhibited significant inhibitory effects against these three human cancer cell lines with IC50 values of 8.54, 3.31, and 6.76 μM, respectively. Additionally, the results from the annexin-V/PI double-staining assay indicated that 1 might inhibit the proliferation of HepG2 cells by inducing apoptosis.

摘要

总共从 Tabernaemontana corymbosa 的叶子中分离得到了 10 种新的吲哚生物碱,即塔伯卡品 A-J(1-10)。塔伯卡品 C-F(3-6)是罕见的 C-14/C-15-断塞托品型单萜吲哚生物碱,并且 5 和 6 是第一个在 C-14 和 C-20 之间具有内酯键的例子。这些生物碱的结构通过光谱方法阐明,并且使用 ECD 激子手性方法确定了 1 和 2 的绝对构型。此外,MTT 测定法用于检查所有新分离物和两种已知分离物对 MCF-7、HepG2 和 SMMC-7721 细胞的生长抑制作用;1 对这三种人癌细胞系具有显著的抑制作用,IC50 值分别为 8.54、3.31 和 6.76 μM。此外, Annexin-V/PI 双重染色测定的结果表明,1 可能通过诱导细胞凋亡来抑制 HepG2 细胞的增殖。

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