Main Article Content

Abstract

In the present study, coumarins were synthesized by reaction of substituted phenols and ethyl acetoacetate in the presence of concentrated sulphuric acid (Pechmann reaction)and substituted with different electro-positive and electronegative groups. The binding affinity of compounds was evaluated by molecular docking in the binding site of phospho-diestrase 4 (PDE4) protein using AutoDockVina and dock scores were calculated. The compounds with good binding affinity were screened for the anti-inflammatory activity using carrageenan induced rat paw edema method. Docking studies showed that compounds 3(d-k) have good binding affinity with PDE4. Further, pharmacological investigation revealed that compound 3(d-e) exhibited highest antiinflammatory activity.

Keywords

Coumarin Anti-Inflammatory Phosphodiestrase inhibitors PDE4B Docking studies

Article Details

How to Cite
Girdhar, A., Raheja, S., Pandita, D., Kharb, V., & Lather, V. (2018). Synthesis, Characterization and Biological Evaluation of Novel Coumarins as Promising Anti-Inflammatory Agents. Asian Journal of Organic & Medicinal Chemistry, 3(4), 150–154. https://doi.org/10.14233/ajomc.2018.AJOMC-P141

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