Asian Journal of Research in Chemistry
  • Year: 2011
  • Volume: 4
  • Issue: 9

Various Methods for Synthesis of Purine Analogues

  • Author:
  • Sachan Dinesh, S.N. Pandeya, A.K. Pathak
  • Total Page Count: 5
  • Page Number: 1361 to 1365

Department of Pharmaceutical Sciences, Saroj Institute of Technology and Management, Lucknow

*Corresponding Author E-mail: sachan1771@gmail.com

Online published on 6 March, 2013.

Abstract

The purine analogues are new class of nonclassical antimicrobial agents that binds with riboswitches. Purine (adenine) analogues are having antimicrobial, antifungal, antitumour, antiproliferative, antiviral and activity against HSV-1. Riboswitches are structured RNA domains that can bind directly to specific ligands and regulate gene expression. These RNA elements are located most commonly within the non-coding regions of bacterial mRNAs, because these genes were involved in fundamental metabolic pathways in certain bacterial pathogens. Purine-binding riboswitches may be targets for the development of novel antimicrobial agents. Designed compounds are bound by a purine riboswitches aptamer in vitro with affinities comparable to that of the natural ligand, and several also inhibit microbial growth.

Keywords

Purines, Synthesis