Abstract
Reaction of 6a-f individually with 2-methylsulfonyl-4,6-dimethoxypyrimidine yielded 7a-f in excellent yield. The newly synthesized heterocycles were characterized by IR, (1)H NMR, and mass spectral data. Compounds 7a-f was screened for their anti-inflammatory activity and were compared with standard drugs. Of the compounds studied, the compound 7e showed more potent activity than the standard drugs at all doses tested.
MeSH terms
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Algorithms
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Animals
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Animals, Inbred Strains
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Anti-Inflammatory Agents, Non-Steroidal / chemical synthesis*
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Anti-Inflammatory Agents, Non-Steroidal / chemistry
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Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
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Disease Models, Animal
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Edema / chemically induced
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Edema / drug therapy
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Edema / prevention & control
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Foot / pathology
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Mice
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Phospholipases A2 / metabolism
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Prostaglandin-Endoperoxide Synthases / metabolism
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Pyrimidines / chemical synthesis*
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Pyrimidines / chemistry
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Pyrimidines / pharmacology*
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Rats
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Ulcer / etiology
Substances
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Anti-Inflammatory Agents, Non-Steroidal
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Pyrimidines
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Prostaglandin-Endoperoxide Synthases
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Phospholipases A2