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Eur J Med Chem ; 42(2): 152-60, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17052805

ABSTRACT

Two series of 1,2,4-triazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles derived from three selected arylpropionic acids namely, ibuprofen, flurbiprofen and naproxen, were synthesized and evaluated for anti-inflammatory activity and ulcerogenic potential. All the tested compounds exhibited anti-inflammatory activity comparable to that of hydrocortisone. Compared to ibuprofen, however, all the tested compounds displayed more potent anti-inflammatory activity. Compounds tested for ulcerogenicity showed no or minimal ulcerogenic effect compared to indomethacin.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/chemical synthesis , Propionates/chemical synthesis , Animals , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Anti-Inflammatory Agents, Non-Steroidal/toxicity , Flurbiprofen/chemistry , Ibuprofen/chemistry , Male , Naproxen/chemistry , Propionates/pharmacology , Propionates/toxicity , Rats , Stomach Ulcer/chemically induced , Structure-Activity Relationship , Thiadiazoles/chemical synthesis , Thiadiazoles/pharmacology , Thiadiazoles/toxicity , Thiazoles/chemical synthesis , Thiazoles/pharmacology , Thiazoles/toxicity
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