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5,6-Cis-penems: broad-spectrum anti-methicillin-resistant Staphylococcus aureus beta-lactam antibiotics
M Ishiguro1, R Tanaka, K Namikawa
1Suntory Institute for Bioorganic Research, Institute for Biomedical Research, Osaka, Japan.
Journal of Medicinal Chemistry
|July 4, 1997
Abstract:
5,6-cis-Penem derivatives have been synthesized and evaluated as anti-MRSA antibiotics. The cis-penems 5 and 6 showed potent activities against not only MRSA but also a wide variety of bacteria including beta-lactamase-producing microorganisms. These compounds were designed to have high affinity to the penicillin-binding protein 2a of MRSA and to form stable acyl intermediates with beta-lactamases by blocking the deacylating water molecule.