| Literature DB >> 30106304 |
Qian Che1, Liang Qiao1, Xiaoning Han1, Yankai Liu1, Wei Wang1, Qianqun Gu1, Tianjiao Zhu1, Dehai Li1,2.
Abstract
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.Entities:
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Year: 2018 PMID: 30106304 DOI: 10.1021/acs.orglett.8b02382
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005