Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-beta-lactam

Org Biomol Chem. 2008 Oct 21;6(20):3823-30. doi: 10.1039/b809221d. Epub 2008 Aug 29.

Abstract

We report herein the synthesis and biological evaluation of bile acid dimers linked through 1,2,3-triazole and bis-beta-lactam. The dimers were synthesized using 1,3-dipolar cycloaddition reaction of diazido bis-beta-lactams , and terminal alkynes derived from cholic acid/deoxycholic acid in the presence of Cu(i) catalyst (click chemistry). These novel molecules were evaluated in vitro for their antifungal and antibacterial activity. Most of the compounds exhibited significant antifungal as well as antibacterial activity against all the tested fungal and bacterial strains. Moreover, their in vitro cytotoxicities towards HEK-293 and MCF-7 cells were also established.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / toxicity
  • Antifungal Agents / chemical synthesis
  • Antifungal Agents / chemistry
  • Antifungal Agents / pharmacology
  • Antifungal Agents / toxicity
  • Cell Line
  • Cell Proliferation / drug effects
  • Cholic Acid / chemical synthesis*
  • Cholic Acid / chemistry
  • Cholic Acid / pharmacology*
  • Cholic Acid / toxicity
  • Deoxycholic Acid / chemical synthesis*
  • Deoxycholic Acid / chemistry
  • Deoxycholic Acid / pharmacology*
  • Deoxycholic Acid / toxicity
  • Dimerization
  • Humans
  • Microbial Sensitivity Tests
  • Triazoles / chemistry*
  • beta-Lactams / chemistry*

Substances

  • Anti-Bacterial Agents
  • Antifungal Agents
  • Triazoles
  • beta-Lactams
  • Deoxycholic Acid
  • Cholic Acid