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-dihydroxy-4-pyridon-2-yl)ethenyl]ceph-3-em-4-carboxylic acid, CP6162 (8e), was selected for further evaluation as an antipseudomonal chemotherapeutic agent. © 1990, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
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CITATION STYLE
Iwamatsu, K., Atsumi, K., Sakagami, K., Ogino, H., Yoshida, T., Tsuruoka, T., … Kondo, S. (1990). A new antipseudomonal cephalosporin CP6162 and its congeners. The Journal of Antibiotics, 43(11), 1450–1463. https://doi.org/10.7164/antibiotics.43.1450
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