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从夹竹桃科鸡骨常山属植物鸡骨常山的枝条中分离得到具有血管舒张活性的新苯丙素类和单萜生物碱。

New phenylpropanoids and monoterpene alkaloids with vasorelaxant activities from the branches of Alstonia scholaris.

机构信息

School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an 710061, PR China.

School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an 710061, PR China.

出版信息

Fitoterapia. 2022 Apr;158:105143. doi: 10.1016/j.fitote.2022.105143. Epub 2022 Feb 4.

Abstract

Two new phenylpropanoids (1-2), one new nor-monoterpenoid alkaloid (3), one new monoterpene alkaloid (4), together with nine known compounds (5-13) were obtained from the branches of Alstonia scholaris. The structures of the undescribed compounds were determined by extensive spectroscopic analysis. Alkaloid 3 represented the first example of C-4 methylated nor-monoterpenoid alkaloids. A possible biosynthetic pathway for this new type of monoterpene alkaloids was proposed. All the isolates were evaluated for vasorelaxant activity against phenylephrine-induced contraction of rat mesenteric arteries. Compounds 1, 4, 9, 12, and 13 showed significant vasorelaxant activity with relaxation rates above 90% at 200 μM and exhibited moderate vasorelaxant activity with IC values ranging from 41.87 to 93.30 μM by further studies. It was the first report on the potential vasorelaxant activity of monoterpene alkaloids. Monoterpene alkaloids 3 and 4 may be served as the potential lead compounds for the discovery of vasodilators, due to their simple and optimizable structures.

摘要

从垂榕的树枝中分离得到两个新的苯丙素类化合物(1-2)、一个新的降单萜类生物碱(3)、一个新的单萜类生物碱(4),以及 9 个已知化合物(5-13)。通过广泛的光谱分析确定了未描述化合物的结构。生物碱 3 代表了第一个 C-4 位甲基化的降单萜类生物碱的例子。提出了这种新型单萜类生物碱的可能生物合成途径。所有分离得到的化合物都被评估了对苯肾上腺素诱导的大鼠肠系膜动脉收缩的血管舒张活性。化合物 1、4、9、12 和 13 在 200 μM 时表现出超过 90%的显著血管舒张活性,并且通过进一步研究,其 IC 值范围在 41.87 至 93.30 μM 之间,表现出中度的血管舒张活性。这是首次报道单萜类生物碱具有潜在的血管舒张活性。由于其简单且可优化的结构,单萜类生物碱 3 和 4 可能成为发现血管扩张剂的潜在先导化合物。

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