Marine Natural Products Team, Institut de Chimie de Nice, Université Côte d'Azur, CNRS, UMR 7272, 06108 Nice, France.
Integrative Biology of Marine Models Laboratory (LBI2M), Station Biologique de Roscoff, Sorbonne Université, CNRS, UMR 8227, 29680 Roscoff, France.
Mar Drugs. 2024 Sep 28;22(10):444. doi: 10.3390/md22100444.
Two new fusarochromanone derivatives, deacetylfusarochromene () and deacetamidofusarochrom-2',3-diene (), along with the previously reported metabolites fusarochromanone TDP-2 (), fusarochromene (), 2,2-dimethyl-5-amino-6-(2'-ene-4'-hydroxylbutyryl)-4-chromone (), fusarochromanone (), (-)-chrysogine (), and equisetin (), were isolated from the marine fungus UBOCC-A-117302. The structures of the compounds were determined by extensive spectrometric (HRMS) and spectroscopic (1D and 2D NMR) analyses, as well as specific rotation. Among them, and showed inhibition of three protein kinases with IC values ranging from 1.42 to 25.48 μM. Cytotoxicity and antimicrobial activity of all isolated compounds were also evaluated. Six fusarochromanone derivatives (-) exhibited diverse activities against three cell lines, RPE-1, HCT-116, and U2OS (IC values ranging from 0.058 to 84.380 μM). Equisetin () showed bactericidal activities against and (MBC values of 7.8 and 31.25 µM, respectively), and bacteriostatic activity against (MIC value of 31.25 µM). Compounds and showed bacteriostatic activities against (MIC of 125 µM).
两种新的呋咱色酮衍生物,去乙酰基呋咱色烯()和去乙酰氨基呋咱-2',3-二烯(),以及之前报道的代谢产物呋咱色酮 TDP-2()、呋咱色烯()、2,2-二甲基-5-氨基-6-(2'-烯-4'-羟丁酰基)-4-色酮()、呋咱色酮()、(-)麦角硫因()和表儿茶素(),从海洋真菌 UBOCC-A-117302 中分离得到。通过广泛的光谱(高分辨质谱)和光谱(1D 和 2D NMR)分析以及比旋光度确定了化合物的结构。其中,和对三种蛋白激酶的抑制活性范围为 1.42-25.48 μM。所有分离得到的化合物的细胞毒性和抗菌活性也进行了评估。六种呋咱色酮衍生物(-)对三种细胞系 RPE-1、HCT-116 和 U2OS 表现出不同的活性(IC 值范围为 0.058-84.380 μM)。表儿茶素()对和(MBC 值分别为 7.8 和 31.25 μM)具有杀菌活性,对(MIC 值为 31.25 μM)具有抑菌活性。化合物和对(MIC 为 125 μM)具有抑菌活性。