Scientific Reports (Jun 2017)

Neo-actinomycins A and B, natural actinomycins bearing the 5H-oxazolo[4,5-b]phenoxazine chromophore, from the marine-derived Streptomyces sp. IMB094

  • Qiang Wang,
  • Yixuan Zhang,
  • Mian Wang,
  • Yi Tan,
  • Xinxin Hu,
  • Hongwei He,
  • Chunling Xiao,
  • Xuefu You,
  • Yiguang Wang,
  • Maoluo Gan

DOI
https://doi.org/10.1038/s41598-017-03769-8
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 8

Abstract

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Abstract Neo-actinomycins A and B (1 and 2), two new natural actinomycins featuring an unprecedented tetracyclic 5H-oxazolo[4,5-b]phenoxazine chromophore, were isolated from the marine-derived actinomycete Streptomyces sp. IMB094. Their structures were elucidated by spectroscopic analyses. The presence of this ring system was proposed to originate from a condensation between actinomycin D (3) with α-ketoglutarate and pyruvate, respectively. Compound 1 showed potent cytotoxic activities against human cancer HCT116 and A549 cell lines in the nanomolar range (IC50: 38.7 and 65.8 nM, respectively) and moderate antibacterial activities against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci (VRE) strains.