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A new antipseudomonal cephalosporin CP6162 and its congeners
K Iwamatsu1, K Atsumi, K Sakagami
1Pharmaceutical Research Center, Meiji Seika Kaisha, Ltd., Yokohama, Japan.
The Journal of Antibiotics
|November 1, 1990
Abstract:
The synthesis and biological activity of a series of 3-[2-(5-hydroxy-4-pyridon-2-yl)ethenyl]cephalosporin derivatives are described. They showed very potent activity against Gram-negative bacteria, especially Pseudomonas aeruginosa. (6R, 7R)-7-[(Z)-2-(2-Aminothiazol-4-yl)-2 -(1-carboxy-1-methyl)-ethoxyiminoacetamido]-3-[(Z)-2-(1,5-dihydrox y-4- pyridon-2-yl)ethenyl]ceph-3-em-4-carboxylic acid, CP6162 (8e), was selected for further evaluation as antipseudomonal chemotherapeutic agent.