Three new phthalide derivatives from culture broth of Dentipellis fragilis and their cytotoxic activities

IF 2.1 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of Antibiotics Pub Date : 2024-03-22 DOI:10.1038/s41429-024-00720-8
Dae-Won Ki, Dae-Cheol Choi, Yeong-Seon Won, Seung-Jae Lee, Young-Hee Kim, In-Kyoung Lee, Bong-Sik Yun
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Abstract

Three new phthalide derivatives (1‒3) together with two known compounds, erinaceolactone B (4) and hericerin III (5), were isolated from the culture broth of Dentipellis fragilis. The chemical structures of 1‒5 were determined by analyses of their 1D-, 2D-NMR, and MS. The absolute configuration of 1 was determined by CD analysis. The isolated compounds were assessed for their cytotoxic activities against A549, DU145, HCT116, and HT1080 cancer cell lines. Compounds 1‒5 showed strong cytotoxic activities against DU145, with IC50 values ranging from 14.3 to 16.1 µM. Additionally, all compounds showed moderate or weak cytotoxic activities against all cell lines except for compounds 4 and 1 which showed no cytotoxic activities against A549 and HCT116 cancer cell lines, respectively. Against HT1080 cancer cell line, only compound 2 displayed moderate cytotoxic activity.

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从脆弱双孢蘑菇培养液中提取的三种新的邻苯二甲酸酯衍生物及其细胞毒性活性。
从脆弱双胞藻的培养液中分离出了三种新的邻苯二甲酸酯衍生物(1-3)以及两种已知化合物麦角内酯 B(4)和麦角素 III(5)。通过一维、二维核磁共振和质谱分析确定了 1-5 的化学结构。通过 CD 分析确定了 1 的绝对构型。评估了分离出的化合物对 A549、DU145、HCT116 和 HT1080 癌细胞株的细胞毒活性。化合物 1-5 对 DU145 具有很强的细胞毒活性,IC50 值为 14.3 至 16.1 µM。此外,除了化合物 4 和 1 分别对 A549 和 HCT116 癌细胞株没有细胞毒性活性外,其他化合物对所有细胞株都显示出中等或较弱的细胞毒性活性。对于 HT1080 癌细胞株,只有化合物 2 显示出中等程度的细胞毒性活性。
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来源期刊
Journal of Antibiotics
Journal of Antibiotics 医学-免疫学
CiteScore
6.60
自引率
3.00%
发文量
87
审稿时长
1 months
期刊介绍: The Journal of Antibiotics seeks to promote research on antibiotics and related types of biologically active substances and publishes Articles, Review Articles, Brief Communication, Correspondence and other specially commissioned reports. The Journal of Antibiotics accepts papers on biochemical, chemical, microbiological and pharmacological studies. However, studies regarding human therapy do not fall under the journal’s scope. Contributions regarding recently discovered antibiotics and biologically active microbial products are particularly encouraged. Topics of particular interest within the journal''s scope include, but are not limited to, those listed below: Discovery of new antibiotics and related types of biologically active substances Production, isolation, characterization, structural elucidation, chemical synthesis and derivatization, biological activities, mechanisms of action, and structure-activity relationships of antibiotics and related types of biologically active substances Biosynthesis, bioconversion, taxonomy and genetic studies on producing microorganisms, as well as improvement of production of antibiotics and related types of biologically active substances Novel physical, chemical, biochemical, microbiological or pharmacological methods for detection, assay, determination, structural elucidation and evaluation of antibiotics and related types of biologically active substances Newly found properties, mechanisms of action and resistance-development of antibiotics and related types of biologically active substances.
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