Abstract
The synthesis of a series of 7-[(Z)-2-(2-aminothiazol-4-yl)-2-oxyiminoacetamido]-3-ammoniomethyl-3-cephems is described. Variations of an oxyimino moiety in the 7-side chain and a quaternary ammonium moiety in the 3-side chain were examined and structure-activity relationships studied. BMY-28142, the 3-(N-methylpyrrolidinio)methyl derivative of the 7-a-methoxyimino series of cephalosporins, exhibited broad antimicrobial activity against both Gram-positive and Gram-negative bacteria including Pseudomonas aeruginosa. © 1986, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
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CITATION STYLE
Naito, T., Aburaki, S., Kamachi, H., Narita, Y., Okumura, J., & Kawaguchi, H. (1986). Synthesis and structure-activity relationships of a new series of cephalosporins, BMY-28142 and related compounds. The Journal of Antibiotics, 39(8), 1092–1107. https://doi.org/10.7164/antibiotics.39.1092
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