Albusamides A-G:深海放线菌 Streptomyces albus 228DD-066 的羟化脂肪胺衍生物及其细胞毒活性。

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL
Journal of Natural Products Pub Date : 2024-10-25 Epub Date: 2024-09-21 DOI:10.1021/acs.jnatprod.4c00683
Hee Jae Shin, Su-Yeon Jung, Jong Soon Kang, Chang-Su Heo, Sun Joo Park
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引用次数: 0

摘要

从大韩民国独岛海岸采集的深海沉积物样本中提取的白链霉菌 228DD-066 的培养液中分离出了一系列新的羟基化脂肪胺衍生物--白桦酰胺 A-G(1-7)和四个已知化合物(8-11),这是首次从天然来源中报道这些化合物。通过对一维和二维核磁共振波谱以及 HRESIMS 进行综合分析,阐明了它们的结构,并使用改进的莫舍法确定了它们的绝对构型。针对实体癌和血癌细胞系的生物学评价显示,这些新的代谢物具有中等到较强的细胞毒性活性。化合物 3 具有很高的细胞毒性,对实体癌细胞株的 GI50 值为 0.4 至 0.6 μM,对 WSU-DLCL2 血癌细胞株的细胞毒性最强(GI50 值 = 0.2 μM)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Albusamides A-G: Hydroxylated Fatty Amine Derivatives from the Deep-Sea-Derived Actinomycete Streptomyces albus 228DD-066 and Their Cytotoxic Activity.

A series of new hydroxylated fatty amine derivatives, albusamides A-G (1-7), along with four known compounds (8-11), which are reported for the first time from a natural source, were isolated from the culture broth of Streptomyces albus 228DD-066 derived from a deep-sea sediment sample gathered off the coast of Dokdo Island, Republic of Korea. Their structures were elucidated through the comprehensive analysis of 1D and 2D NMR spectra and HRESIMS, and absolute configurations were determined using the modified Mosher's method. Biological evaluations against solid and blood cancer cell lines revealed that these new metabolites have moderate to strong cytotoxic activity. Compound 3 exhibited high cytotoxic activity with GI50 values ranging from 0.4 to 0.6 μM against solid cancer cell lines and exhibited the strongest cytotoxicity (GI50 value = 0.2 μM) against the WSU-DLCL2 blood cancer cell line.

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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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