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赫曲烯酮 A,一种来自夏威夷火山土壤相关真菌Penicillium herquei FT729 的独特的重排苯醌-色满酮。

Herqueilenone A, a unique rearranged benzoquinone-chromanone from the Hawaiian volcanic soil-associated fungal strain Penicillium herquei FT729.

机构信息

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.

出版信息

Bioorg Chem. 2020 Dec;105:104397. doi: 10.1016/j.bioorg.2020.104397. Epub 2020 Oct 21.

Abstract

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.

摘要

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。

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