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白蚁巢药用真菌纤孔菌中异戊烯基酚醚类化合物。

Isoprenyl phenolic ethers from the termite nest-derived medicinal fungus Xylaria fimbriata.

机构信息

Graduate Institute of Pharmacognosy, Taipei, Taiwan.

The Ph.D. Program for the Clinical Drug Discovery from Botanical Herbs, Taipei Medical University, Taipei, Taiwan.

出版信息

J Food Drug Anal. 2019 Jan;27(1):111-117. doi: 10.1016/j.jfda.2018.05.007. Epub 2018 Jun 18.

Abstract

Seven new isoprenyl phenolic ethers, namely fimbriethers A‒G (1‒7), were isolated from the fermented broth of the termite nest-derived medicinal fungus Xylaria fimbriata YMJ491. Their structures were determined by spectroscopic data analysis and compared with those reported. The effects of all the isolates at a concentration of 100 μM on the inhibition of nitric oxide (NO) production in lipopolysaccharide (LPS)-induced murine macrophage RAW 264.7 cells were evaluated, and all of them exhibited NO production inhibitory activity with E values ranging from 4.6 ± 2.0% to 49.7 ± 0.5% without significant cytotoxicity. In addition, these seven compounds did not alter phenylephrine-induced vasocontraction in isolated intact thoracic aortic rings from C57BL/6J mouse, indicating 1‒7 were not involved in the regulation of endothelial NOS-mediated NO production.

摘要

从白蚁巢来源的药用真菌黄韧革菌 YMJ491 的发酵液中分离得到了 7 个新的异戊烯基酚醚类化合物,分别命名为 fimbriethers A-G(1-7)。通过光谱数据分析确定了它们的结构,并与已报道的结构进行了比较。在 100 μM 浓度下,所有分离物对脂多糖(LPS)诱导的鼠巨噬细胞 RAW 264.7 细胞中一氧化氮(NO)产生的抑制作用进行了评估,结果显示它们均具有 NO 产生抑制活性,半数有效值(E 值)范围为 4.6±2.0%至 49.7±0.5%,且无明显细胞毒性。此外,这 7 种化合物在分离的 C57BL/6J 小鼠完整胸主动脉环中对苯肾上腺素诱导的血管收缩没有影响,表明 1-7 不参与内皮型一氧化氮合酶(eNOS)介导的 NO 产生的调节。

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