Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2011 Nov 8;1(1):15.
doi: 10.1186/2191-2858-1-15.

Synthesis of new pyrazolyl-2, 4-thiazolidinediones as antibacterial and antifungal agents

Affiliations

Synthesis of new pyrazolyl-2, 4-thiazolidinediones as antibacterial and antifungal agents

Deepak K Aneja et al. Org Med Chem Lett. .

Abstract

Background: Thiazolidine-2, 4-diones (TZDs) have become a pharmacologically important class of heterocyclic compounds since their introduction in the form of glitazones into the clinical use for the treatment of type 2 diabetes. TZDs lower the plasma glucose levels by acting as ligands for gamma peroxisome proliferators-activated receptors. In addition, this class of heterocyclic compounds possesses various other biological activities such as antihyperglycemic, antimicrobial, anti-inflammatory, anticonvulsant, insecticidal, etc. TZDs are also known for lowering the blood pressure thereby reducing the chances of heart failure and micro-albuminuria in the patients with type 2 diabetes.

Results: We have described herein the synthesis of three series of compounds, namely, ethyl 2-((Z)-5-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)-2, 4-dioxothiazolidin-3-yl)acetates (4), methyl 2-((Z)-5-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)-2, 4-dioxothiazolidin-3-yl)acetates (5), and 2-((Z)-5-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)-2, 4-dioxothiazolidin-3-yl)acetic acids (6). The compounds 4 and 5 were synthesized by Knoevenagel condensation between 3-aryl-1-phenyl-1H-pyrazole-4-carbaldehydes (1) and ethyl/methyl 2-(2, 4-dioxothiazolidin-3-yl)acetates (3, 2) in alcohol using piperidine as a catalyst. The resultant compounds 4 and 5 having ester functionality were subjected to acidic hydrolysis to obtain 6. All the new compounds were tested for their in vitro antibacterial and antifungal activity.

Conclusions: Knoevenagel condensation approach has offered an easy access to new compounds 4-6. Antimicrobial evaluation of the compounds has shown that some of the compounds are associated with remarkable antifungal activity. In case of antibacterial activity, these were found to be effective against Gram-positive bacteria. However, none of the compounds were found to be effective against Gram-negative bacteria.

PubMed Disclaimer

Figures

Scheme 1
Scheme 1
Synthesis of pyrazolyl-2, 4-TZDs (4-6).

Similar articles

Cited by

References

    1. Berber I, Cokmus C, Atalan E. Characterization of Staphylococcus species by SDS-PAGE of whole cell and extracellular proteins. Microbiology. 2003;72:42–47. doi: 10.1023/A:1022221905449. - DOI - PubMed
    1. Bildirici I, Sener A, Tozlu I. Further derivatives of 4-benzoyl-1, 5-diphenyl-1H pyrazole-3-carboxylic acid and their antibacterial activities. Med Chem Rev. 2007;16:418–426. doi: 10.1007/s00044-007-9082-z. - DOI
    1. Sung WS, Jung HJ, Park K, Kim HS, Lee Ln-S, Lee DG. 2, 5-Dimethyl-4-hydroxy-3(2H)-furanone (DMHF): antimicrobial compound with cell cycle arrest in nosocomial pathogens. Life Sci. 2007;80:586–591. doi: 10.1016/j.lfs.2006.10.008. - DOI - PubMed
    1. Aggarwal R, Kumar V, Tyagi P, Singh SP. Synthesis and antibacterial activity of some new 1-heteroaryl-5-amino-3H/methyl-4-phenylpyrazoles. Bioorg Med Chem. 2006;14:1785–1791. doi: 10.1016/j.bmc.2005.10.026. - DOI - PubMed
    1. Kumar V, Aggarwal R, Tyagi P, Singh SP. Synthesis and antibacterial activity of some new 1-heteroaryl-5-amino-4-phenyl-3-trifluoromethylpyrazoles. Eur J Med Chem. 2005;40:922–927. doi: 10.1016/j.ejmech.2005.03.021. - DOI - PubMed

LinkOut - more resources