Abstract
A regioisomeric set of 2-naphthylcarbapenems featuring cationic substituents was synthesized. Optimal placement of the cationic group was found to markedly improve activity against methicillin-resistant staphylococci while maintaining a good spectrum of gram-negative activity.
MeSH terms
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Anti-Bacterial Agents / chemical synthesis*
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Anti-Bacterial Agents / pharmacology
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Carbapenems / chemical synthesis*
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Carbapenems / pharmacology
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Dipeptidases / metabolism
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Methicillin Resistance*
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Molecular Structure
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Naphthalenes / chemical synthesis*
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Naphthalenes / pharmacology
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Staphylococcus / drug effects*
Substances
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Anti-Bacterial Agents
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Carbapenems
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Naphthalenes
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Dipeptidases
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dipeptidase