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J Pharm Sci ; 81(4): 365-6, 1992 Apr.
Article in English | MEDLINE | ID: mdl-1501075

ABSTRACT

Ten new substituted 2-mercapto-3-(N-aryl)pyrimido[5,4-c]cinnolin-4- (3H)-ones (4) were prepared by refluxing substituted 4-aminocinnolin-3-carboxylic acid (3) with substituted arylisothiocyanate in anhydrous pyridine. These derivatives were evaluated for their antimicrobial and anti-inflammatory activities. Some of the title compounds possess potent antimicrobial activity.


Subject(s)
Anti-Bacterial Agents/chemical synthesis , Anti-Inflammatory Agents, Non-Steroidal/chemical synthesis , Pyridazines/chemical synthesis , Pyrimidines/chemical synthesis , Animals , Anti-Bacterial Agents/pharmacology , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Carrageenan , Edema/chemically induced , Edema/drug therapy , Escherichia coli/drug effects , Female , Male , Microbial Sensitivity Tests , Pseudomonas aeruginosa/drug effects , Pyridazines/pharmacology , Pyrimidines/pharmacology , Rats
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