School of Pharmacy, Sungkyunkwan University, Suwon 16419, Republic of Korea.
Daniel K. Inouye College of Pharmacy, University of Hawaii at Hilo, Hilo, HI 96720, United States.
Bioorg Chem. 2020 Dec;105:104397. doi: 10.1016/j.bioorg.2020.104397. Epub 2020 Oct 21.
The study of a Hawaiian volcanic soil-associated fungal strain Penicillium herquei FT729 led to the isolation of one unprecedented benzoquinone-chromanone, herqueilenone A (1) and two phenalenone derivatives (2 and 3). Their structures were determined through extensive analysis of NMR spectroscopic data and gauge-including atomic orbital (GIAO) NMR chemical shifts and ECD calculations. Herqueilenone A (1) contains a chroman-4-one core flanked by a tetrahydrofuran and a benzoquinone with an acetophenone moiety. Plausible pathways for the biosynthesis of 1-3 are proposed. Compounds 2 and 3 inhibited IDO1 activity with IC values of 14.38 and 13.69 μM, respectively. Compounds 2 and 3 also demonstrated a protective effect against acetaldehyde-induced damage in PC-12 cells.
对一株来源于夏威夷火山土壤的真菌菌株青霉(Penicillium herquei)FT729 的研究导致了一个前所未有的苯醌-色满酮类化合物——赫奎烯酮 A(1)以及两个菲咯啉酮衍生物(2 和 3)的分离。通过对 NMR 谱数据和基于赝原子轨道(GIAO)NMR 化学位移和 ECD 计算的广泛分析,确定了它们的结构。赫奎烯酮 A(1)包含一个色满-4-酮核心,两侧分别为四氢呋喃和苯醌,带有苯乙酮部分。提出了 1-3 的可能生物合成途径。化合物 2 和 3 对 IDO1 活性的抑制作用的 IC50 值分别为 14.38 和 13.69 μM。化合物 2 和 3 还对乙醛诱导的 PC-12 细胞损伤表现出保护作用。