Taipei Medical University

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Sun CH
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------>journal_name=Abstr. Cong. Chinese Pharm. Soc.
------>paper_name=Synthesis and stability of cefotaxime prodrugs
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------>fullAbstract=The synthesis and biological properties of the new penem antibiotic MEN 10700 (6) and of its selected oral prodrug MEN 11505 (8f) are described. MEN 10700 showed a broad spectrum of activity, with high potency both on Gram-positive and Gram-negative strains. It also exhibited good antibacterial activity toward anaerobes and on strains selected for their resistance to other antibacterial agents (cefotaxime- or ceftazidime-resistant Gram-negative strains, ciprofloxacin-resistant E. coli, extended spectrum beta-lactamase producing and cephalosporinase inducible enterobacteria). MEN 10700 showed a very high stability to enzymatic degradation by renal dehydropeptidase DHP-I. After oral administration in rats of the pivaloyloxymethyl ester prodrug MEN 11505, the relative bioavailability of MEN 10700 was calculated as F=43%.
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------>authors2=Lee JS
------>authors3=Wang HP
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------>authors=Sun CH
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------>updateTitle=Synthesis and biological activity of the penem antibiotic MEN 10700 and its orally absorbed ester MEN 11505.
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------>publish_year=1995
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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z