Antiviral Rotenoids and Isoflavones Isolated from Millettia oblata ssp. teitensis

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL Journal of Natural Products Pub Date : 2024-04-05 DOI:10.1021/acs.jnatprod.3c01288
Ivan Kiganda, Jonathan Bogaerts, Lianne H. E. Wieske, Tsegaye Deyou, Yoseph Atilaw, Colores Uwamariya, Masum Miah, Joanna Said, Albert Ndakala, Hoseah M. Akala, Wouter Herrebout, Edward Trybala, Tomas Bergström*, Abiy Yenesew* and Mate Erdelyi*, 
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Abstract

Three new (13) and six known rotenoids (510), along with three known isoflavones (1113), were isolated from the leaves of Millettia oblata ssp. teitensis. A new glycosylated isoflavone (4), four known isoflavones (1418), and one known chalcone (19) were isolated from the root wood extract of the same plant. The structures were elucidated by NMR and mass spectrometric analyses. The absolute configuration of the chiral compounds was established by a comparison of experimental ECD and VCD data with those calculated for the possible stereoisomers. This is the first report on the use of VCD to assign the absolute configuration of rotenoids. The crude leaves and root wood extracts displayed anti-RSV (human respiratory syncytial virus) activity with IC50 values of 0.7 and 3.4 μg/mL, respectively. Compounds 6, 8, 10, 11, and 14 showed anti-RSV activity with IC50 values of 0.4–10 μM, while compound 3 exhibited anti-HRV-2 (human rhinovirus 2) activity with an IC50 of 4.2 μM. Most of the compounds showed low cytotoxicity for laryngeal carcinoma (HEp-2) cells; however compounds 3, 11, and 14 exhibited low cytotoxicity also in primary lung fibroblasts. This is the first report on rotenoids showing antiviral activity against RSV and HRV viruses.

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从稗属植物中分离出的抗病毒轮状病毒素和异黄酮类物质
从扁平黍(Millettia oblata ssp. teitensis)的叶片中分离出了 3 种新的(1-3)和 6 种已知的类蔷薇酮(5-10),以及 3 种已知的异黄酮(11-13)。从同一种植物的根木提取物中分离出了一种新的糖基化异黄酮(4)、四种已知的异黄酮(14-18)和一种已知的查尔酮(19)。通过核磁共振和质谱分析阐明了这些化合物的结构。通过比较实验 ECD 和 VCD 数据与可能立体异构体的计算数据,确定了手性化合物的绝对构型。这是首次报道使用 VCD 来确定石蒜酸的绝对构型。粗叶和根木提取物具有抗 RSV(人类呼吸道合胞病毒)活性,IC50 值分别为 0.7 和 3.4 μg/mL。化合物 6、8、10、11 和 14 具有抗 RSV 活性,IC50 值为 0.4-10 μM,而化合物 3 具有抗 HRV-2(人鼻病毒 2)活性,IC50 值为 4.2 μM。大多数化合物对喉癌(HEp-2)细胞的细胞毒性较低;但化合物 3、11 和 14 对原发性肺成纤维细胞的细胞毒性也较低。这是第一份关于类橙皮苷对 RSV 和 HRV 病毒具有抗病毒活性的报告。
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来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
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