13-Deoxo-13-iminodutomycin, a new neuroprotective compound from Streptomyces sp. RAP78

J Antibiot (Tokyo). 2022 Jan;75(1):40-43. doi: 10.1038/s41429-021-00488-1. Epub 2021 Nov 26.

Abstract

A neuroprotective compound (2) was isolated from the culture broth of the dutomycin (1) producer Streptomyces sp. RAP78. The molecular formula of 2 was established as C44H55NO16 by high-resolution FAB-MS. The structure was determined to be a new dutomycin derivative possessing an acetimidoyl group in place of an acetyl group by NMR spectroscopic analysis. 13-Deoxo-13-iminodutomycin (2) but not dutomycin (1) protected C6 rat glioma cells and N18-RE-105 rat primary retina-mouse neuroblastoma hybrid cells from glutamate-induced toxicity with EC50s of 0.12 µM and 0.72 µM, respectively.

MeSH terms

  • Animals
  • Anthracyclines
  • Cell Death / drug effects
  • Cell Line, Tumor
  • Drug Discovery
  • Glutamic Acid / toxicity
  • Magnetic Resonance Spectroscopy
  • Mice
  • Molecular Structure
  • Neuroprotective Agents / isolation & purification
  • Neuroprotective Agents / pharmacology*
  • Rats
  • Spectrometry, Mass, Fast Atom Bombardment
  • Streptomyces / chemistry*

Substances

  • Anthracyclines
  • Neuroprotective Agents
  • dutomycin
  • Glutamic Acid