Article ID Journal Published Year Pages File Type
1394088 European Journal of Medicinal Chemistry 2014 10 Pages PDF
Abstract

•Compounds 1f–i, 2e, 2f and 2i were found to be most potent in in vitro assay.•Compounds 1f, 1g and 2e displayed better anti-inflammatory activity than ibuprofen in vivo.•Compounds 1f displayed good ADMET profile, similar to naproxen.

Nepodin and chrysophanol, isolated from Rumex nepalensis roots, showed significant cyclooxygenase (COX) inhibitory activity. To further optimize these lead molecules and study structure activity relationship (SAR), eighteen derivatives of nepodin and nine derivatives of chrysophanol were synthesized and evaluated for COX-1 and COX-2 inhibitory potential. Among the synthesized compounds, four nepodin (1f, 1g, 1h and 1i) and three chrysophanol (2e, 2f and 2h) derivatives displayed more pronounced COX-2 inhibition than their respective lead molecule. Further, compounds 1f, 1g, 2e and 2h exhibited better anti-inflammatory activity than ibuprofen in carrageenan-induced rat paw edema assay. Taking into account the in vitro and in vivo results, molecular docking and in silico prediction of ADMET properties of compounds were carried out respectively.

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Physical Sciences and Engineering Chemistry Organic Chemistry
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