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Antinociceptive properties of caffeic acid derivatives in mice.

European journal of medicinal chemistry (2009-07-25)
Fátima de Campos Buzzi, Caroline Liandra Franzoi, Graziele Antonini, Mauricio Fracasso, Valdir Cechinel Filho, Rosendo Augusto Yunes, Rivaldo Niero
ZUSAMMENFASSUNG

Ten ester derivatives from caffeic acid were synthesized, and their antinociceptive properties are evaluated in mice. The most active compound, dodecyl ester derivative, exhibited potent and dose-related activity against the writhing test, with a calculated ID(50) value of 15.1 (11.9-19.1)micromol/kg and MI of 78.8% being several times more active than reference drugs. It was also effective in other experimental models, such as formalin, capsaicin and glutamate-induced pain tests, but was inactive in the hot-plate test. Although the mechanism of action has still not been elucidated, these results appear to support its therapeutic potential against painful diseases.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Kaffeesäure, ≥98.0% (HPLC)
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Acetylsalicylsäure, ≥99.0%
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4-Acetamidophenol, BioXtra, ≥99.0%
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Aspirin, meets USP testing specifications
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4-Acetamidophenol, meets USP testing specifications, 98.0-102.0%, powder
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4-Acetamidophenol, analytical standard
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Acetylsalicylsäure, analytical standard
Supelco
Kaffeesäure, suitable for matrix substance for MALDI-MS, ≥99.0% (HPLC)