Angucycline Glycosides from Mangrove-Derived Streptomycesdiastaticus subsp. SCSIO GJ056

Mar Drugs. 2018 May 28;16(6):185. doi: 10.3390/md16060185.

Abstract

Nine new angucycline glycosides designated urdamycins N1⁻N9 (19), together with two known congener urdamycins A (10) and B (11), were obtained from a mangrove-derived Streptomycesdiastaticus subsp. SCSIO GJ056. The structures of new compounds were elucidated on the basis of extensive spectroscopic data analysis. The absolute configurations of 69 were assigned by electronic circular dichroism calculation method. Urdamycins N6 (6) and N9 (9) represent the first naturally occurring (5R, 6R)-angucycline glycosides, which are diastereomers of urdamycins N7 (7) and N8 (8), respectively.

Keywords: angucycline; mangrove-derived Streptomyces; urdamycin.

MeSH terms

  • Aminoglycosides / chemistry*
  • Aminoglycosides / isolation & purification
  • Anthraquinones / chemistry*
  • Anthraquinones / isolation & purification
  • Anti-Bacterial Agents / chemistry*
  • Anti-Bacterial Agents / isolation & purification
  • Aquatic Organisms / metabolism*
  • Circular Dichroism
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Streptomyces / metabolism*
  • Wetlands

Substances

  • Aminoglycosides
  • Anthraquinones
  • Anti-Bacterial Agents