Abstract
The synthesis and the pharmacological activity of a series of 1-aroyl derivatives of kynurenic acid methyl ester (4-oxo-quinolin-2-carboxy methyl (KYNA) esters), structurally related to NSAID indomethacin are described. The derivatives were screened in vivo for anti-inflammatory and analgesic activities. Most of the compounds exhibited good anti-inflammatory and analgesic activities. An automatic docking of the synthesized compounds was performed using X-ray structures of COX-1 and COX-2. Docking results are in good accordance with the experimental biological data.
MeSH terms
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Analgesics / chemical synthesis*
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Analgesics / chemistry
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Analgesics / metabolism
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Analgesics / pharmacology*
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Animals
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Anti-Inflammatory Agents / chemical synthesis*
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Anti-Inflammatory Agents / chemistry
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Anti-Inflammatory Agents / metabolism
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Anti-Inflammatory Agents / pharmacology*
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Carrageenan / chemistry
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Carrageenan / metabolism
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Cyclooxygenase 1 / pharmacology
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Cyclooxygenase 2 / chemistry
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Cyclooxygenase 2 / metabolism
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Cyclooxygenase 2 / pharmacology
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Drug Evaluation, Preclinical
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Indomethacin / pharmacology
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Kynurenic Acid / analogs & derivatives*
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Kynurenic Acid / chemical synthesis*
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Kynurenic Acid / chemistry
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Kynurenic Acid / pharmacology*
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Models, Molecular
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Rats
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Structure-Activity Relationship
Substances
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Analgesics
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Anti-Inflammatory Agents
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Carrageenan
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Cyclooxygenase 1
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Cyclooxygenase 2
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Kynurenic Acid
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Indomethacin