Metabolites of Streptomyces sp., an endophytic actinomycete from Alpinia oxyphylla

Nat Prod Res. 2014;28(4):265-7. doi: 10.1080/14786419.2013.830219. Epub 2013 Aug 25.

Abstract

Four known compounds had been isolated from the Streptomyces sp. YIM66017, and their structures were elucidated by spectral analysis as 2,6-dimethoxy terephthalic acid (1), yangjinhualine A (2), α-hydroxyacetovanillone (3) and cyclo(Gly-Trp) (4). Compound 1 was isolated from natural resources for the first time, and compounds 2-4 were isolated from streptomycetes for the first time. The 2,2-diphenyl-1-picrylhydrazyl radical-scavenging activity assays showed that 1 showed higher activity than rutin with IC50 of 4.61 μg/mL and 2 showed the activity with IC50 of 57.12 μg/mL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alpinia / microbiology
  • Biphenyl Compounds / pharmacology
  • Dipeptides / chemistry
  • Dipeptides / isolation & purification
  • Free Radical Scavengers / chemistry
  • Free Radical Scavengers / isolation & purification*
  • Free Radical Scavengers / pharmacology
  • Inhibitory Concentration 50
  • Molecular Structure
  • Peptides, Cyclic / chemistry
  • Peptides, Cyclic / isolation & purification
  • Phthalic Acids / chemistry
  • Phthalic Acids / isolation & purification*
  • Phthalic Acids / pharmacology
  • Picrates / pharmacology
  • Rutin / pharmacology
  • Streptomyces / chemistry*

Substances

  • 2,6-dimethoxy terephthalic acid
  • Biphenyl Compounds
  • Dipeptides
  • Free Radical Scavengers
  • Peptides, Cyclic
  • Phthalic Acids
  • Picrates
  • cyclo(glycyltryptophyl)
  • Rutin
  • 1,1-diphenyl-2-picrylhydrazyl