The Journal of Antibiotics
Online ISSN : 1881-1469
Print ISSN : 0021-8820
ISSN-L : 0021-8820
Studies on Anti-MRSA Parenteral Cephalosporins I. Synthesis and Antibacterial Activity of 7β-[2-(5-Amino-l52, 4-thiadiazol-3-yl)-2(Z)-hydroxyiminoacetamido]-3-(substituted imidazo[1, 2-6]-pyridazinium-1-yl)methyl-3-cephem-4-carboxylates and Related Compounds
TOMOYASU ISHIKAWAYIJJI IIZAWAKENJI OKONOGIAKIO MIYAKE
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2000 Volume 53 Issue 10 Pages 1053-1070

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Abstract

In order to improve the antibacterial activity of cefozopran (CZOP) against methicillin-resistant Staphylococcus aureus (MRSA), we initiated chemical modification to introduce a 2-(5-amino-1, 2, 4-thiadiazol-3-yl)-2(Z)-hydroxyimino acetyl group at the C-7 position and a 3- or 6-substituted imidazo[1, 2-b]pyridazinium or 5-substituted imidazo[1, 2-a]pyridmium group at the C-3' position. Although this approach successfully enhanced the anti-MRSA activity of CZOP two to eight times, a slight decrease in the activity against Gram-negative bacteria including Pseudomonas aeruginosa was involved. Among the novel derivatives, 3-(6-aminoimidazo[1, 2-b]pyridazinium-1-yl)methyl-7β-[2-(5-amino-1, 2, 4-thiadiazol-3-yl)-2(Z)-hydroxyiminoacetamido]-3-cephem-4-carboxylate (44a) showed an excellent balance of activity against MRSA and Gram-negative bacteria.

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