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胡豆素 A-E,结构多样的野豌豆属种子衍生的金雀花碱衍生物。

Hosimosines A-E, structurally diverse cytisine derivatives from the seeds of Ormosia hosiei Hemsl. et Wils.

机构信息

Department of Pharmacy, College of Medicine, Jiaxing University, Jiaxing 314001, China.

Department of Pharmacy, College of Medicine, Jiaxing University, Jiaxing 314001, China.

出版信息

Fitoterapia. 2023 Oct;170:105661. doi: 10.1016/j.fitote.2023.105661. Epub 2023 Aug 28.

DOI:10.1016/j.fitote.2023.105661
PMID:37648030
Abstract

Ormosia hosiei Hemsl. et Wils (Fabaceae family) is an arbor species endemic to China. The seeds of O. hosiei have been used as traditional Chinese medicine to treat hernia, abdominal pain, blood stasis and amenorrhea. Cytisine-like and angustifoline type alkaloids were main components identified from this plant. In our research on the bioactive alkaloids from the promising Chinese medicinal plants, four new angustifoline type alkaloids (1-4) and a new cytisine-like alkaloid (5), named hosimosine A-E, together with 13 known analogues (6-18) were isolated from the seeds of O. hosiei. Their structures were elucidated by the extensive spectroscopic methods, especially the interpretation of NMR spectra and specific rotations, along with the methods of NMR and ECD calculation. Compounds 1-4 were identified as two pairs of epimers, whose relative configurations were deduced from density functional theory (DFT) calculations of NMR chemical shifts and DP4+ analysis, and absolute configurations were determined by comparison of their experimental and theoretical ECD spectra. Compound 5 displayed two sets of NMR data caused by the existence of tautomeric forms. Compounds 14, 17 and 18 were determined to be enantiomers of literature compounds. Some of the isolates exhibited moderate cytotoxic effects against HepG2, A2780 and MCF-7 cells.

摘要

Ormosia hosiei Hemsl. et Wils(豆科)是一种中国特有的乔木物种。该植物的种子被用作传统中药,用于治疗疝气、腹痛、血瘀和闭经。从这种植物中鉴定出的细胞碱和安格司丁型生物碱是主要成分。在我们对有前途的中药植物生物活性生物碱的研究中,从 O. hosiei 的种子中分离得到了四个新的安格司丁型生物碱(1-4)和一个新的细胞碱类似物(5),命名为 hosimosine A-E,以及 13 个已知类似物(6-18)。通过广泛的光谱方法,特别是 NMR 光谱和比旋光度的解释,以及 NMR 和 ECD 计算方法,阐明了它们的结构。化合物 1-4 被鉴定为两对差向异构体,其相对构型是根据 NMR 化学位移和 DP4+分析的密度泛函理论(DFT)计算推断的,绝对构型是通过比较其实验和理论 ECD 光谱确定的。化合物 5 显示出两组由互变异构形式引起的 NMR 数据。化合物 14、17 和 18 被确定为文献化合物的对映异构体。一些分离物对 HepG2、A2780 和 MCF-7 细胞表现出中等的细胞毒性作用。

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