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1.
J Antibiot (Tokyo) ; 39(1): 121-7, 1986 Jan.
Article in English | MEDLINE | ID: mdl-3485088

ABSTRACT

7 beta-[2-(2-Aminooxazol-4-yl)-2-Z-methoximinoacetamido]-3-cep hem -4-carboxylic acids 12 and 13 were synthesized. The microbiological activity of 12 and 13 as well as the beta-lactamase stability of 12 were discussed. Both 12 and 13 were quite active against a wide variety of microorganisms although usually less active than cefotaxime.


Subject(s)
Anti-Bacterial Agents/chemical synthesis , Cephalosporins/chemical synthesis , Anti-Bacterial Agents/pharmacology , Bacteria/drug effects , Cefotaxime/pharmacology , Cephalosporins/pharmacology , Magnetic Resonance Spectroscopy , Microbial Sensitivity Tests , beta-Lactamases/metabolism
2.
J Antibiot (Tokyo) ; 39(1): 111-20, 1986 Jan.
Article in English | MEDLINE | ID: mdl-3485087

ABSTRACT

A series of 7 beta-[2-(5-aminooxadiazol-3-yl)-2-Z-methoximinoacetamido] -3-cephem-4-carboxylic acids (7a-g) were synthesized and evaluated microbiologically Although somewhat less active than cefotaxime 7a-g showed good antimicrobial activity against a wide variety of Gram-positive and Gram-negative bacteria. The beta-lactamase stability of 7a and 7f was also discussed.


Subject(s)
Cephalosporins/chemical synthesis , Cephalosporins/pharmacology , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Microbial Sensitivity Tests , Models, Molecular , beta-Lactamases/metabolism
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