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来自 Commiphora africana(A. Rich.)Endl. 的白藜芦醇衍生物对多种人癌细胞系显示细胞毒性和选择性。

Resveratrol derivatives from Commiphora africana (A. Rich.) Endl. display cytotoxicity and selectivity against several human cancer cell lines.

机构信息

Department of Pharmacognosy, Faculty of Pharmacy, University of Ibadan, Ibadan, Nigeria.

Medicinal Chemistry and Natural Products Research Group, School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, UK.

出版信息

Phytother Res. 2019 Jan;33(1):159-166. doi: 10.1002/ptr.6209. Epub 2018 Oct 22.

Abstract

Commiphora africana (A. Rich.) Endl. (Burseraceae) is a medicinal plant widely used in Nigerian ethnomedicine. The in vitro cytotoxicity of the stem bark extract of C. africana and isolated cytotoxic compounds was investigated. Three resveratrol derivatives: (E)-resveratrol 3-O-rutinoside (1), 5-methoxy-(E)-resveratrol 3-O-rutinoside (2), and pinostilbene (3), together with 3-hydroxy-5-methoxybenzoic acid (4) were isolated from the methanol fraction of C. africana. Their structures were determined by extensive analysis of their HREIMS and NMR spectra. The cytotoxicity of the isolated compounds against four human carcinoma cells was determined using the MTT assay. Compound 1 displayed the highest antiproliferative effect on the cell lines, with IC values of 16.80, 21.74, 17.89, and 17.44 μM, against MCF7, A549, PC3, and HepG2 human cancer cell lines, respectively. In addition, compounds 1-3 showed low toxicity against normal human prostate cell line, with selectivity indices greater than five across the carcinoma cells, indicating that the compounds possess potential in the development of low-toxicity chemotherapeutic agents. These results support the traditional use of this plant in the treatment of cancer.

摘要

非洲没药(A. Rich.)Endl.(没药科)是一种在尼日利亚传统医学中广泛使用的药用植物。本文研究了其茎皮提取物及分离得到的细胞毒性化合物的体外细胞毒性。从非洲没药甲醇部位分离得到了 3 个白藜芦醇衍生物:(E)-白藜芦醇 3-O-鼠李糖苷(1)、5-甲氧基-(E)-白藜芦醇 3-O-鼠李糖苷(2)和紫檀芪(3),以及 3-羟基-5-甲氧基苯甲酸(4)。通过对其 HREIMS 和 NMR 谱的综合分析确定了它们的结构。采用 MTT 法测定了分离得到的化合物对 4 个人癌细胞系的细胞毒性。化合物 1 对 MCF7、A549、PC3 和 HepG2 人癌细胞系的增殖抑制作用最强,IC 值分别为 16.80、21.74、17.89 和 17.44 μM。此外,化合物 1-3 对正常前列腺细胞的毒性较低,对癌细胞的选择性指数均大于 5,表明这些化合物在开发低毒性化疗药物方面具有潜力。这些结果支持了该植物在癌症治疗中的传统用途。

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