Design, Synthesis and Biological Activities of Thiazolyl-pyrazole-bis-coumarins

In this study, we report the synthesis of thiazolyl-pyrazole-biscoumarins employing hydrochloric acid as an effective catalyst. The synthesized derivatives were subjected to biological evaluation for anti-inflammatory, antioxidant and antimicrobial activities. The results indicate that the oxygen containing heterocycles among the synthesized compounds exhibited notable anti-inflammatory and antioxidant properties while sulfur containing heterocycles demonstrated promising antimicrobial efficacy. This work highlights the potential of these thiazolyl-pyrazole-biscoumarin derivatives as multifunctional agents in therapeutic applications.

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Publication Details

Journal
Asian Journal of Chemistry
Published
2024-12-31
DOI
https://doi.org/10.14233/ajchem.2025.32981
Primary Topic
Synthesis and biological activity
Type
article
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article

Design, Synthesis and Biological Activities of Thiazolyl-pyrazole-bis-coumarins

Y.B. Basavaraju, Nisha Chiriapanda Lohith, K. KUMAR, K. Prakruthi Aiyappa
Asian Journal of Chemistry
Synthesis and biological activity
article

Design, Synthesis and Biological Activities of Thiazolyl-pyrazole-bis-coumarins

Y.B. Basavaraju, Nisha Chiriapanda Lohith, K. KUMAR, K. Prakruthi Aiyappa
article en

Abstract

In this study, we report the synthesis of thiazolyl-pyrazole-biscoumarins employing hydrochloric acid as an effective catalyst. The synthesized derivatives were subjected to biological evaluation for anti-inflammatory, antioxidant and antimicrobial activities. The results indicate that the oxygen containing heterocycles among the synthesized compounds exhibited notable anti-inflammatory and antioxidant properties while sulfur containing heterocycles demonstrated promising antimicrobial efficacy. This work highlights the potential of these thiazolyl-pyrazole-biscoumarin derivatives as multifunctional agents in therapeutic applications.

Asian Journal of ChemistryVol. 37(1)
University of Mysore (IN)
Clean water and sanitation
Openalex Percentile: Top 82%
Synthesis and biological activity
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