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一种来自海洋黑芋螺内共生真菌XXH003的具有多种生物活性的环肽。

A Multiple Biological Activities Cyclopeptide From Endophytic Fungus Phaeosphaeria Sp. XXH003 of the Marine Conus literatus.

作者信息

Lin Ying-Ting, Liu Jie, Huang Zhou, Hu An-Qi, Liu Yu-Hang, Zhang Zhi-Hao, Dong Shuai

机构信息

Key Laboratory of Tropical Biological Resources of Ministry of Education, School of Pharmaceutical Sciences, Hainan University, Haikou, P. R. China.

China Pharmaceutical University, Nanjing, P. R. China.

出版信息

Chem Biodivers. 2025 Aug;22(8):e202403141. doi: 10.1002/cbdv.202403141. Epub 2025 Apr 26.

Abstract

Chemical investigation of the endophytic fungus Phaeosphaeria sp. XXH003 isolated from Conus literatus was conducted. Eleven compounds were isolated and identified as ergosterol (1), β-sitosterol (2), ergosterol peroxide (3), ergosta-4,6,8(14),22-tetraen-3-one (4), 1,1'-oxybis(2,4-di-tert-butylbenzene) (5), 5-[(1S)-1-hydroxybutyl]-6-methyl-2H-pyran-2-one (6), quinolactacin C1/C2 (7/8), cyclodepsipeptide Sch 217048 (9), linoleic acid (10), and oleic acid (11), respectively. Their structures were determined by nuclear magnetic resonance and mass spectrometry. All compounds were isolated from Phaeosphaeria sp. for the first time, and the content of compound 9 was as high as 250 mg/kg rice culture medium. Compound 9 showed inhibitory effects on renal fibrosis at concentrations of 10 and 20 µM, leading to reduced expression of three types of fibrous-related proteins in the human kidney 2 cells, including fibronectin, collagen I, and vimentin. At a concentration of 100 µM, compound 9 extended the lifespan of Caenorhabditis elegans by 14.77%. Compound 9 demonstrated both anti-vesicular stomatitis virus and anti-herpes simplex virus activity at a concentration of 15 and 20 µM. In addition, none of the compounds showed anti-glioma cell line U87MG activity or lipotropic activity, and compounds 1, 2, 3, and 9 did not exhibit neuroprotective activity.

摘要

对从线纹芋螺中分离得到的内生真菌Phaeosphaeria sp. XXH003进行了化学研究。分离并鉴定出11种化合物,分别为麦角甾醇(1)、β-谷甾醇(2)、过氧化麦角甾醇(3)、麦角甾-4,6,8(14),22-四烯-3-酮(4)、1,1'-氧双(2,4-二叔丁基苯)(5)、5-[(1S)-1-羟基丁基]-6-甲基-2H-吡喃-2-酮(6)、喹诺拉辛C1/C2(7/8)、环缩肽Sch 217048(9)、亚油酸(10)和油酸(11)。通过核磁共振和质谱确定了它们的结构。所有化合物均首次从Phaeosphaeria sp.中分离得到,化合物9在水稻培养基中的含量高达250 mg/kg。化合物9在10和20 μM浓度下对肾纤维化具有抑制作用,导致人肾2细胞中三种纤维相关蛋白(包括纤连蛋白、I型胶原蛋白和波形蛋白)的表达降低。在100 μM浓度下,化合物9使秀丽隐杆线虫的寿命延长了14.77%。化合物9在15和20 μM浓度下表现出抗水泡性口炎病毒和抗单纯疱疹病毒活性。此外,这些化合物均未表现出抗胶质瘤细胞系U87MG活性或促脂活性,化合物1、2、3和9也未表现出神经保护活性。

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