“Unveiling the anti-inflammatory potential of coumarin-based Schiff base derivatives through structural characterization and in vitro and in vivo biological evaluation”

BACKGROUND: Chronic inflammation contributes to several diseases, creating a need for effective anti-inflammatory agents. OBJECTIVE: This study aimed to synthesize, characterize, and evaluate coumarin-based Schiff base derivatives for anti-inflammatory activity. METHODS: activity using carrageenan-induced paw edema in Wistar rats. Molecular docking was performed against COX-2 protein structures, and drug-likeness and ADME properties were predicted using SwissADME. RESULTS: activity, producing 82.65% and 73.46% inhibition of protein denaturation, respectively, at 250 µg/mL. At 200 mg/kg, SB-5 and SB-6 produced 46.02% and 41.29% inhibition of paw edemarespectively, whereas diclofenac sodium produced 66.90% inhibition at the dose evaluated. Both compounds were well tolerated in the acute toxicity study. Molecular docking indicated favorable interactions with COX-2 targets. SwissADME analysis showed compliance with Lipinski and Veber criteria and favorable gastrointestinal absorption and pharmacokinetic properties. CONCLUSION: SB-5 and SB-6 demonstrated promising preliminary anti-inflammatory activity and warrant further target-specific, pharmacological, pharmacokinetic, and toxicity studies to validate their potential for drug development.

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Publication Details

Journal
Future Medicinal Chemistry
Published
2026-11-09
DOI
https://doi.org/10.1080/17568919.2026.2754124
Primary Topic
Heterocyclic Compound Synthesis and Bioactivity
Type
article
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article

“Unveiling the anti-inflammatory potential of coumarin-based Schiff base derivatives through structural characterization and in vitro and in vivo biological evaluation”

Pradeepkumar M. Ronad, Akshata S. Menasinakai, Arpita F. Hiremath
Future Medicinal Chemistry
Heterocyclic Compound Synthesis and Bioactivity
article

“Unveiling the anti-inflammatory potential of coumarin-based Schiff base derivatives through structural characterization and in vitro and in vivo biological evaluation”

Pradeepkumar M. Ronad, Akshata S. Menasinakai, Arpita F. Hiremath
article en

Abstract

BACKGROUND: Chronic inflammation contributes to several diseases, creating a need for effective anti-inflammatory agents. OBJECTIVE: This study aimed to synthesize, characterize, and evaluate coumarin-based Schiff base derivatives for anti-inflammatory activity. METHODS: activity using carrageenan-induced paw edema in Wistar rats. Molecular docking was performed against COX-2 protein structures, and drug-likeness and ADME properties were predicted using SwissADME. RESULTS: activity, producing 82.65% and 73.46% inhibition of protein denaturation, respectively, at 250 µg/mL. At 200 mg/kg, SB-5 and SB-6 produced 46.02% and 41.29% inhibition of paw edemarespectively, whereas diclofenac sodium produced 66.90% inhibition at the dose evaluated. Both compounds were well tolerated in the acute toxicity study. Molecular docking indicated favorable interactions with COX-2 targets. SwissADME analysis showed compliance with Lipinski and Veber criteria and favorable gastrointestinal absorption and pharmacokinetic properties. CONCLUSION: SB-5 and SB-6 demonstrated promising preliminary anti-inflammatory activity and warrant further target-specific, pharmacological, pharmacokinetic, and toxicity studies to validate their potential for drug development.

Future Medicinal Chemistry
KLE Academy of Higher Education and Research (IN)
Heterocyclic Compound Synthesis and Bioactivity
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