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从红藻衍生真菌银耳目真菌NTOU4196中分离得到的具有抑制小胶质细胞一氧化氮生成活性的海松烷型倍半萜。

Hirsutane-Type Sesquiterpenes with Inhibitory Activity of Microglial Nitric Oxide Production from the Red Alga-Derived Fungus Chondrostereum sp. NTOU4196.

作者信息

Hsiao George, Chi Wei-Chiung, Pang Ka-Lai, Chen Jih-Jung, Kuo Yueh-Hsiung, Wang Yu-Kai, Cha Hyo-Jung, Chou Shen-Chieh, Lee Tzong-Huei

机构信息

Graduate Institute of Medical Science and Department of Pharmacology, College of Medicine, Taipei Medical University , Taipei 11031, Taiwan.

Department of Food Science, National Quemoy University , Kinmen 89250, Taiwan.

出版信息

J Nat Prod. 2017 May 26;80(5):1615-1622. doi: 10.1021/acs.jnatprod.7b00196. Epub 2017 May 17.

Abstract

The marine red alga Pterocladiella capillacea is an economic alga for the food industry in Taiwan, and its associated highly diversified fungi have not been investigated meticulously thus far. The EtOAc extract of the fermented broth of Chondrostereum sp. NTOU4196, a fungal strain isolated from P. capillacea, was found to exhibit significant nitric oxide (NO) production inhibitory activity in lipopolysaccharide-activated murine RAW 264.7 cells at a concentration of 100 μg/mL in the preliminary screening. Therefore, separation of the active principles from the fermented broths was performed, and that has led to the isolation of eight new 5,5,5-tricyclic hirsutane-type sesquiterpenes, namely, chondroterpenes A-H (1-8), together with seven known analogues. They were identified by analyses of spectroscopic data and comparison with literature values. Among the new isolates, chondroterpene A (1) exhibited more significant NO production inhibitory activity in murine BV-2 microglial cells, and of all the isolated compounds, hirsutanol A (9) exerted limited cytotoxic effects and the most potent inhibitory activity on NO production.

摘要

海洋红藻纤细拟羽藻是台湾食品工业中的一种经济藻类,迄今为止,其相关的高度多样化真菌尚未得到细致研究。从纤细拟羽藻中分离出的真菌菌株Chondrostereum sp. NTOU4196发酵液的乙酸乙酯提取物,在初步筛选中发现,在浓度为100μg/mL时,对脂多糖激活的小鼠RAW 264.7细胞具有显著的一氧化氮(NO)生成抑制活性。因此,对发酵液中的活性成分进行了分离,从而分离出8个新的5,5,5-三环刺柏烷型倍半萜,即软骨萜A-H(1-8),以及7个已知类似物。通过光谱数据分析并与文献值比较对它们进行了鉴定。在新分离出的化合物中,软骨萜A(1)在小鼠BV-2小胶质细胞中表现出更显著的NO生成抑制活性,在所有分离出的化合物中,刺柏醇A(9)具有有限的细胞毒性作用,并且对NO生成具有最有效的抑制活性。

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