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来自印度尼西亚链霉菌属的安古环素类化合物

Angucyclinones from an Indonesian Streptomyces sp.

作者信息

Fotso Serge, Mahmud Taifo, Zabriskie T Mark, Santosa Dwi Andreas, Proteau Philip J

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, Corvallis 97331-3507, USA.

出版信息

J Nat Prod. 2008 Jan;71(1):61-5. doi: 10.1021/np0704102. Epub 2007 Dec 15.

Abstract

Six new angucyclinone polyketides named panglimycins A-F were isolated together with the three known metabolites (+)-fujianmycin A, (+)-ochromycinone, and emycin C from the bioassay-guided fractionation of the extract of the Indonesian Streptomyces strain ICBB8230. The new compounds are highly oxygenated angucyclinones that appear to be biosynthetically derived from ochromycinone or fujianmycin. Their structures were determined by X-ray crystal analysis, interpretation of 1D- and 2D-NMR spectra, and comparison of the data with those of structurally related known natural products. Despite structural similarities to angucyclinones with antibiotic activities, the panglimycins did not exhibit any growth inhibition when tested against several bacteria and fungi.

摘要

从印度尼西亚链霉菌菌株ICBB8230提取物的生物活性导向分馏中,分离出六种新的安古环素聚酮化合物,命名为盘里霉素A - F,同时还分离出三种已知代谢产物(+)-福建霉素A、(+)-赭曲霉素酮和红霉素C。这些新化合物是高度氧化的安古环素,似乎是由赭曲霉素酮或福建霉素生物合成而来。它们的结构通过X射线晶体分析、一维和二维核磁共振光谱的解析以及与结构相关的已知天然产物的数据比较来确定。尽管盘里霉素与具有抗生素活性的安古环素在结构上有相似之处,但在针对几种细菌和真菌进行测试时,盘里霉素没有表现出任何生长抑制作用。

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