4.5 Article

Three New Chromone Derivatives Produced by Phomopsis sp HNY29-2B from Acanthus ilicifolius Linn.

期刊

CHINESE JOURNAL OF CHEMISTRY
卷 35, 期 12, 页码 1889-1893

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cjoc.201700375

关键词

phomochromenones; Phomopsis sp; absolution configurations; electronic circular dichroism; cytotoxicity

资金

  1. National Natural Science Foundation of China [21472251, 41276146]
  2. Key Project of Natural Science Foundation of Guangdong Province [2016A030311026]
  3. Science & Technology Plan Project of Guangdong Province of China [2013B021100011, 2016A040403091]
  4. Special Financial Fund of Innovative Development of Marine Economic Demonstration Project [GD2012-D01-001]
  5. China's Marine Commonweal Research Project [201305017]
  6. Guangzhou Project of Science & Technology Planning [201300000062]
  7. Fundamental Research Funds for the Central Universities [141gjc16]
  8. Supercomputing Center of Chinese Academy of Sciences (SCCAS)

向作者/读者索取更多资源

Three new chromone derivatives, phomochromenones A-C (1-3), and one known chaetocyclinone B (4) were obtained from the cultures of Phomopsis sp. HNY29-2B isolated from the mangrove Acanthus ilicifolius Linn., which was collected from the South China Sea. Their structures were determined by the analysis of D-1 NMR and D-2 NMR as well as mass spectroscopic data. The absolute configurations of 1 and 2 were assigned by quantum chemical calculations of the electronic circular dichroism (ECD) spectra. Compound 3 is the third example of alkaloids possessing the unique chromeno [3,2-c] pyridine nucleus. In the bioactivity assay, compound 4 showed cytotoxicity against human prostate cancer cell lines (PC-3 and DU145 cells) with the IC50 values of 8.13 and 3.59 mu mol/L, respectively.

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