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- W2068654319 abstract "A new series of ketoprofen analogs were synthesized to evaluate their biological activities as selective cyclooxygenase-2 (COX-2) inhibitors. In vitro COX-1 and COX-2 inhibition studies showed that all compounds were potent and selective inhibitors of the COX-2 isozyme with IC50 values in the highly potent 0.057–0.085 μM range, and COX-2 selectivity indexes in the 115 to >1298.7 range. Compounds possessing azido pharmacophore group (8a and 8b) exhibited highly COX-2 inhibitory selectivity and potency even more than reference drug celecoxib. Molecular modeling studies indicated that the azido substituent can be inserted deeply into the secondary pocket of COX-2 active site for interactions with Arg513." @default.
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- W2068654319 date "2010-08-01" @default.
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- W2068654319 title "Design, synthesis, and biological evaluation of ketoprofen analogs as potent cyclooxygenase-2 inhibitors" @default.
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- W2068654319 doi "https://doi.org/10.1016/j.bmc.2010.06.094" @default.
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