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Aldgamycins Q 和 Q 是两种新型的 16 元大环内酯类化合物,来自罕见放线菌 Saccharothrix sp. 16Sb2-4。

Aldgamycins Q and Q two novel 16-membered macrolides from the rare actinomycete Saccharothrix sp. 16Sb2-4.

机构信息

Department of Microbial Chemistry, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, 100050, Beijing, China.

出版信息

J Antibiot (Tokyo). 2024 Dec;77(12):842-846. doi: 10.1038/s41429-024-00775-7. Epub 2024 Sep 25.

Abstract

Two novel 16-membered macrolides, named aldgamycin Q (1) and Q (2), were isolated from the culture broth of the rare actinomycete Saccharothrix sp. 16Sb2-4. The structures of 1 and 2 were elucidated as new aldgamycin analogs with a demethylated mycinose residue by spectroscopic analyses and comparison with data of aldgamycin K. Compounds 1 and 2 showed moderate to weak antibacterial activities against Enterococcus faecalis, Bacillus subtilis, Staphylococcus aureus and Acinetobacter baumannii, with MIC values ranging from 16 to 64 μg mL.

摘要

从稀有放线菌 Saccharothrix sp. 16Sb2-4 的发酵液中分离得到两种新型 16 元大环内酯类化合物,命名为 aldgamycin Q (1) 和 Q (2)。通过光谱分析和与 aldgamycin K 的数据比较,阐明了 1 和 2 的结构为具有去甲基 mycinose 残基的新型 aldgamycin 类似物。化合物 1 和 2 对粪肠球菌、枯草芽孢杆菌、金黄色葡萄球菌和鲍曼不动杆菌表现出中等至弱的抗菌活性,MIC 值范围为 16 至 64μg/mL。

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