Ph.D. Program in Clinical Drug Development of Herbal Medicine, College of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan.
Department of Pharmacy, Faculty of Health Science, University of Muhammadiyah Mataram, Mataram 83127, Indonesia.
Mar Drugs. 2022 Jan 18;20(2):80. doi: 10.3390/md20020080.
Eight trichothecenes, including four new compounds - and four known entities -, together with one known cyclonerane () were isolated from the solid-state fermentation of NTU439 isolated from the marine alga . The structures of - were determined by 1D/2D NMR (nuclear magnetic resonance), MS (mass spectrometry), and IR (infrared spectroscopy) spectroscopic data. All of the compounds were evaluated for cytotoxic activity against HCT-116, PC-3, and SK-Hep-1 cancer cells by the SRB assay, and compound showed promising cytotoxic activity against all three cancer cell lines with the IC values of 3.3 ± 0.3, 5.3 ± 0.3, and 1.8 ± 0.8 μM, respectively. Compounds -, -, and - potently inhibited LPS-induced NO production, and compounds and showed markedly inhibited gelatinolysis of MMP-9 in S1 protein-stimulated THP-1 monocytes.
从海洋藻类中分离出的菌株 NTU439 的固态发酵产物中分离得到了 8 种单端孢霉烯族化合物，包括 4 种新化合物和 4 种已知化合物，以及一种已知的环二萜。通过 1D/2D NMR（核磁共振）、MS（质谱）和 IR（红外光谱）光谱数据确定了 - 的结构。采用 SRB 法测定了所有化合物对 HCT-116、PC-3 和 SK-Hep-1 癌细胞的细胞毒性活性，化合物 对三种癌细胞系均显示出有希望的细胞毒性活性，IC 值分别为 3.3 ± 0.3、5.3 ± 0.3 和 1.8 ± 0.8 μM。化合物 -、- 和 - 强烈抑制 LPS 诱导的 NO 产生，化合物 和 显著抑制 S1 蛋白刺激的 THP-1 单核细胞中 MMP-9 的明胶酶解。
Zotero 插件
