Structure-activity relationships (SAR) of triazine derivatives: Promising antimicrobial agents

Eur J Med Chem. 2020 Jan 1:185:111804. doi: 10.1016/j.ejmech.2019.111804. Epub 2019 Oct 23.

Abstract

The emergence of drug resistance has created unmet medical need for the development of new classes of antibiotics. Innovation of new antibacterial agents with new mode of action remains a high priority universally. Triazines are six-membered, nitrogen-containing heterocyclic scaffold with a wide range of pharmaceutical properties such as antibacterial, antifungal, anticancer, antioxidants, antitubercular, antimalarial, anti-HIV, anticonvulsant, anti-inflammatory, antiulcer, and analgesic activities. The present review focuses on the recent developments in the area of medicinal chemistry to discover various chemical structures as potential antimicrobial agents and their structure-activity relationships (SAR) studies are also discussed for further rational design of this kind of derivatives.

Keywords: Antibacterial; Antifungal; Minimum inhibitory concentration; SAR; Triazines.

Publication types

  • Review

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Bacteria / drug effects*
  • Humans
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Triazines / chemistry
  • Triazines / pharmacology*
  • Viruses / drug effects*

Substances

  • Anti-Bacterial Agents
  • Antiviral Agents
  • Triazines