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Eur J Med Chem ; 44(11): 4596-602, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19628311

ABSTRACT

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.


Subject(s)
Analgesics/chemistry , Analgesics/therapeutic use , Caffeic Acids/chemistry , Caffeic Acids/therapeutic use , Pain/drug therapy , Animals , Mice , Molecular Structure , Pain/chemically induced , Structure-Activity Relationship
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