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  2. One pot three components microwave assisted and conventional synthesis of new 3-(4-chloro-2-hydroxyphenyl)-2-(substituted) thiazolidin-4-one as antimicrobial agents

One pot three components microwave assisted and conventional synthesis of new 3-(4-chloro-2-hydroxyphenyl)-2-(substituted) thiazolidin-4-one as antimicrobial agents

  • Bioorg Med Chem Lett. 2014 Aug 1;24(15):3569-73. doi: 10.1016/j.bmcl.2014.05.051.
Dattatraya N Pansare 1 Nayeem A Mulla 2 Chandrakant D Pawar 1 Vikas R Shende 2 Devanand B Shinde 3
Affiliations

Affiliations

  • 1 Department of Chemical Technology, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad 431 004, MS, India.
  • 2 Department of Biochemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad 431 004, MS, India.
  • 3 Department of Chemical Technology, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad 431 004, MS, India. Electronic address: dbsdattatraya10@rediffmail.com.
Abstract

A one-pot, three-component, microwave assisted and conventional synthesis of new 3-(4-chloro-2-hydroxyphenyl)-2-(substituted) thiazolidin-4-one (4a-n) was carried out by using N,N-dimethylformamide as a solvent with high product yield. Among these synthesized compounds (4f, 4g, 4l and 4m) were found to be a broad spectrum molecule active against all Bacterial and fungus strains tested, except fungus Aspergillus niger. Amongst the compounds (4g, 4l and 4m) were found to be more potent than respective standard drugs used in the experiment against Candida albicans, Staphylococcus aureus and Aspergillus flavus, respectively. All synthesized compounds were also tested for their cytotoxic activity against HeLa and MCF-7 cell lines by the sulforhodamine B (SRB) assay. This study shows that all compounds were non-cytotoxic in nature, and confirmed their antimicrobial specificity apart from any general cytotoxicity.

Keywords

2-Amino-5-chlorophenol; Antimicrobial; Cytotoxicity; Microwave-assisted synthesis; Thiazolidin-4-one.

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