Abstract
A series of coumarin analogs, designed and synthesised as potential fluorescent zinc probes were evaluated for their biological activity as anti-inflammatory and antioxidant agents. The effect of the synthesised compounds on inflammation, using the carrageenin-induced rat paw oedema model, was studied. In general, the compounds were found to be potent anti-inflammatory agents (26.5-64%). Compound 5 was found to interact significantly with 1,1-diphenyl-2-picryl-hydrazyl stable free radical (DPPH) whereas the remainder were inactive in this assay. The compounds inhibit in general the soybean lipoxygenase and scavenge superoxide anion radicals. The anti-inflammatory activity seems to be connected with their reducing activity. Their RM values were determined as an expression of their lipophilicity. Theoretical calculations of their lipophilicity as clog P were performed indicating that only a poor relationship exists between their lipophilicity and anti-inflammatory activity.
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Hadjipavlou-Litina, D., Kontogiorgis, C., Pontiki, E., Dakanali, M., Akoumianaki, A., & Katerinopoulos, H. E. (2007). Anti-inflammatory and antioxidant activity of coumarins designed as potential fluorescent zinc sensors. Journal of Enzyme Inhibition and Medicinal Chemistry, 22(3), 287–292. https://doi.org/10.1080/14756360601073914
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