Yatakemycin: total synthesis, DNA alkylation, and biological properties

Nat Prod Rep. 2008 Apr;25(2):220-6. doi: 10.1039/b705665f. Epub 2007 Nov 6.

Abstract

DNA-binding small molecules are an important source of anticancer therapeutics that display a diverse array of mechanisms of action. Synthetic studies on the new DNA-alkylating natural product yatakemycin, detailed in this Highlight, have served to reassign its structure, assign the absolute stereochemistry, and provide access to yatakemycin and a series of structural analogues for biological evaluation. Studies on the DNA alkylation properties of (+)-and ent-(-)-yatakemycin and related analogues have demonstrated the enhanced DNA alkylation properties of this class of agents and provided insight into their interaction with DNA.

MeSH terms

  • Alkylation
  • Crystallography, X-Ray
  • DNA / chemistry*
  • Duocarmycins
  • Indoles* / chemical synthesis
  • Indoles* / chemistry
  • Indoles* / pharmacology
  • Molecular Conformation
  • Molecular Structure
  • Pyrroles* / chemical synthesis
  • Pyrroles* / chemistry
  • Pyrroles* / pharmacology
  • Stereoisomerism

Substances

  • Duocarmycins
  • Indoles
  • Pyrroles
  • yatakemycin
  • DNA