Anthranosides A-C, Anthranilate Derivatives from a Sponge-Derived Streptomyces sp. CMN-62.
Qian CheLiang QiaoXiaoning HanYan-Kai LiuWei WangQianqun GuTianjiao ZhuDe-Hai LiPublished in: Organic letters (2018)
Three new derivatives, anthranosides A-C (1-3), were discovered from a marine sponge-derived actinomycete Streptomyces sp. CMN-62. Their structures including absolute configurations were elucidated using MS and NMR spectroscopic data, X-ray single-crystal diffraction analysis, and chemical synthesis. Compounds 1 and 2 are epimers composed by linking the anthranilate unit to the fructofuranose moiety via a carbon-nitrogen bond, while 3 possessed a unique indole-containing scaffold. All compounds were tested for cytotoxicity, anti-influenza H1N1 virus, and NFκB inhibitory activities, and 3 showed anti-influenza activity. A possible Amadori rearrangement-based biosynthetic pathway was proposed to generate compounds 1-3.
Keyphrases
- high resolution
- mass spectrometry
- multiple sclerosis
- magnetic resonance
- molecular docking
- ms ms
- electronic health record
- lps induced
- big data
- nuclear factor
- magnetic resonance imaging
- computed tomography
- structure activity relationship
- electron microscopy
- pi k akt
- cell proliferation
- toll like receptor
- tissue engineering
- crystal structure