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Amphidinol 22 a New Cytotoxic and Antifungal Amphidinol from the Dinoflagellate Amphidinium carterae

机译:Amphidinol 22一种新的细胞毒性和抗真菌Amphidinol来自鞭毛双歧杆菌。

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摘要

Due to the unique biodiversity and the physical-chemical properties of their environment, marine microorganisms have evolved defense and signaling compounds that often have no equivalent in terrestrial habitats. The aim of this study was to screen extracts of the dinoflagellate Amphidinium carterae for possible bioactivities (i.e., anticancer, anti-inflammatory, anti-diabetes, antibacterial and antifungal properties) and identify bioactive compounds. Anticancer activity was evaluated on human lung adenocarcinoma (A549), human skin melanoma (A2058), human hepatocellular carcinoma (HepG2), human breast adenocarcinoma (MCF7) and human pancreas carcinoma (MiaPaca-2) cell lines. Antimicrobial activities were evaluated against Gram-positive bacteria (Staphylococcus aureus MRSA and MSSA), Gram-negative bacteria (i.e., Escherichia coli and Klebsiella pneumoniae), Mycobacterium tuberculosis and the fungus Aspergillus fumigatus. The results indicated moderate biological activities against all the cancer cells lines and microorganisms tested. Bioassay-guided fractionation assisted by HRMS analysis allowed the detection of one new and two known amphidinols that are potentially responsible for the antifungal and cytotoxic activities observed. Further isolation, purification and structural elucidation led to a new amphidinol, named amphidinol 22. The planar structure of the new compound was determined by analysis of its HRMS and 1D and 2D NMR spectra. Its biological activity was evaluated, and it displayed both anticancer and antifungal activities.
机译:由于其独特的生物多样性及其环境的物理化学特性,海洋微生物已经进化出防御和信号传导化合物,这些化合物在陆地生境中通常不具有相同的功能。这项研究的目的是为可能的生物活性(即抗癌,抗炎,抗糖尿病,抗菌和抗真菌特性)筛选双鞭毛角叉菜角叉菜提取物并鉴定生物活性化合物。在人肺腺癌(A549),人皮肤黑素瘤(A2058),人肝细胞癌(HepG2),人乳腺腺癌(MCF7)和人胰腺癌(MiaPaca-2)细胞系中评估了抗癌活性。评估了对革兰氏阳性菌(金黄色葡萄球菌MRSA和MSSA),革兰氏阴性菌(即大肠杆菌和肺炎克雷伯菌),结核分枝杆菌和烟曲霉菌的抗菌活性。结果表明针对所有测试的癌细胞系和微生物具有中等生物活性。在HRMS分析的辅助下,生物测定指导的分馏可以检测到一种可能与观察到的抗真菌和细胞毒活性有关的新的和两种已知的两性酚。进一步的分离,纯化和结构阐明产生了一种新的两性酚,称为两性酚22。通过分析其HRMS以及1D和2D NMR光谱确定了该新化合物的平面结构。对它的生物学活性进行了评估,并显示出抗癌和抗真菌活性。

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