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具有抗氧化和细胞毒性活性的从倒心叶木和厚叶木中分离得到的细胞毒酮类化合物。

Cytotoxic xanthones isolated from Calophyllum depressinervosum and Calophyllum buxifolium with antioxidant and cytotoxic activities.

机构信息

Centre for Natural Product Research and Drug Discovery (CENAR), Wellness Research Cluster, Jalan Universiti, 50603, Kuala Lumpur, Wilayah Persekutuan, Kuala Lumpur, Malaysia.

Department of Chemistry, Faculty of Science, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.

出版信息

Food Chem Toxicol. 2019 Nov;133:110800. doi: 10.1016/j.fct.2019.110800. Epub 2019 Aug 31.

DOI:10.1016/j.fct.2019.110800
PMID:31479710
Abstract

The stem bark of Calophyllum depressinervosum and Calophyllum buxifolium were extracted and examined for their antioxidant activities, together with cytotoxicity towards human cancer cells. The methanol extract of C. depressinervosum exhibited good DPPH and NO scavenging effects. The strongest BCB inhibition and FIC effects were shown by dichloromethane and ethyl acetate extracts of both species. Overall, DPPH, FRAP and FIC assays showed strong correlation with TPC. For cytotoxicity, hexane extract of C. depressinervosum possessed the strongest anti-proliferative activities towards SNU-1 cells while the hexane extract of C. buxifolium showed the strongest activity towards LS-174T and K562 cells with the IC values ranging from 7 to 17 μg/mL. The purification of plant extracts afforded eight xanthones, ananixanthone (1), caloxanthone B (2), caloxanthone I (3), caloxanthone J (4) xanthochymone B (5), thwaitesixanthone (6), 1,3,5,6-tetrahydroxyxanthone (7) and dombakinaxanthone (8). All the xanthones, except 1 were reported for the first time from both Calophyllum species. The xanthones were examined for their cytotoxic effect against K562 leukemic cells. Compounds 1 and 2 showed strong cytotoxicity with the IC values of 2.96 and 1.23 μg/mL, respectively. The molecular binding interaction of 2 was further investigated by performing molecular docking study with promising protein receptor Src kinase.

摘要

金叶厚皮香和厚叶木茎皮提取物的抗氧化活性及对人癌细胞的细胞毒性研究。金叶厚皮香甲醇提取物对 DPPH 和 NO 有良好的清除作用。两种植物的二氯甲烷和乙酸乙酯提取物对 BCB 抑制和 FIC 作用最强。总体而言,DPPH、FRAP 和 FIC 测定与 TPC 呈强相关性。细胞毒性实验表明,金叶厚皮香正己烷提取物对 SNU-1 细胞的增殖活性最强,而厚叶木正己烷提取物对 LS-174T 和 K562 细胞的活性最强,IC 值范围为 7 至 17 μg/mL。植物提取物的纯化得到了 8 种酮类化合物,分别为:ananixanthone(1)、caloxanthone B(2)、caloxanthone I(3)、caloxanthone J(4)、xanthochymone B(5)、thwaitesixanthone(6)、1,3,5,6-四羟基酮(7)和 dombakinaxanthone(8)。除 1 外,所有酮类化合物均首次从这两种金叶厚皮香中分离得到。对这些酮类化合物进行了对 K562 白血病细胞的细胞毒性试验。化合物 1 和 2 表现出较强的细胞毒性,IC 值分别为 2.96 和 1.23 μg/mL。进一步通过与有前途的蛋白受体Src 激酶进行分子对接研究,研究了化合物 2 的分子结合相互作用。

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