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海洋来源真菌 Aspergillus sp. 产生的抗菌蒽醌二聚体

Antibacterial anthraquinone dimers from marine derived fungus Aspergillus sp.

机构信息

School of Pharmacy, Nantong University, Nantong 226001, PR China.

Key Laboratory of Modern Preparation of TCM, Jiangxi University of Traditional Chinese Medicine, Ministry of education, Nanchang 330004, PR China.

出版信息

Fitoterapia. 2019 Mar;133:1-4. doi: 10.1016/j.fitote.2018.11.015. Epub 2018 Dec 10.

Abstract

As a continue investigation of the bioactive secondary metabolites from marine derived fungi, two new anthraquinone dimers (1, 2), along with three known anthraquinones (3-5) and two known xanthones (6, 7) were isolated from the marine-derived fungus Aspergillus versicolor. Their structures, including the absolute configurations, were elucidated by NMR, HRMS, and comparison with reported ones. Among them, compounds 1 and 2 were identified as anthraquinone dimers which dimerized by a rare C-O-C ether linkage, and both of them showed selective antibacterial activity against Gram-positive Staphylococcus aureus; whilst compound 6 exhibited moderate cytotoxicity against human cancer cell lines.

摘要

作为对海洋来源真菌中生物活性次生代谢产物的持续研究,从海洋来源真菌青霉(Aspergillus versicolor)中分离得到了两个新的蒽醌二聚体(1、2),以及三个已知的蒽醌(3-5)和两个已知的黄烷酮(6、7)。通过 NMR、HRMS 以及与文献报道的比较,确定了它们的结构,包括绝对构型。其中,化合物 1 和 2 被鉴定为蒽醌二聚体,它们通过罕见的 C-O-C 醚键二聚化,两者均表现出对革兰氏阳性金黄色葡萄球菌的选择性抗菌活性;而化合物 6 对人癌细胞系显示出中等的细胞毒性。

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