Synthesis and biological activities of 8-substituted 2-5A analogues

Nucleic Acids Symp Ser. 1990:(22):13-4.

Abstract

The 8-(2-hydroxypropyl)-adenosine and 8-hydroxy adenosine-substituted analogues of 2-5A and it's derivatives were synthesized and their biological activity was evaluated in mouse L cell extracts. The 8-hydroxy adenosine-substituted analogues (i.e. pppAOH2'p5AOH2'p5'AOH, pAOH2'p5'AOH2'p5'AOH, pppA2'p5'A2'p5'AOH, pA2'p5'A2'p5'AOH) inhibited protein synthesis with a relative activity compared to the parent 2-5A. Further, the greater interest is the observation that the corresponding 5'-monophosphate had to inhibitory activity. However, 8-(2-hydroxypropyl)-adenosine substituted analogue (pAHPr2'p5'AHPr2'p5'AHPr) can not about bound as well as parent 2-5A.

MeSH terms

  • Adenine Nucleotides / chemistry*
  • Adenine Nucleotides / pharmacology
  • Adenosine / analogs & derivatives
  • Adenosine / chemistry
  • Animals
  • Endoribonucleases / metabolism
  • Enzyme Activation / drug effects
  • L Cells
  • Mice
  • Oligoribonucleotides / chemistry*
  • Oligoribonucleotides / pharmacology
  • RNA, Ribosomal / metabolism

Substances

  • Adenine Nucleotides
  • Oligoribonucleotides
  • RNA, Ribosomal
  • 8-(2-hydroxypropyl)adenosine
  • 8-oxoadenosine
  • 2',5'-oligoadenylate
  • Endoribonucleases
  • 2-5A-dependent ribonuclease
  • Adenosine