New carbapenem derivatives

The carbapenem derivatives represented by the following formula (I) is disclosed. These compounds have strong anti-bacterial activities against bacteria including methicillin resistant Staphylococcus aureus, penicillin resistant Streptococcus pneumoniae, Enterococci, influenza, and beta -lactamase p...

Full description

Saved in:
Bibliographic Details
Main Authors KAZUHIRO AIHARA, YUKO KANO, KATSUYOSHI IWAMATSU, KAZUKO KOBAYASHI, TAKASHI IDA, KUNIO ATSUMI, TOSHIRO SASAKI, YUMIKO TOYOOKA, HIROMASA TAKIZAWA, KENICHI FUSHIHARA
Format Patent
LanguageEnglish
Published 22.03.2001
Edition6
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The carbapenem derivatives represented by the following formula (I) is disclosed. These compounds have strong anti-bacterial activities against bacteria including methicillin resistant Staphylococcus aureus, penicillin resistant Streptococcus pneumoniae, Enterococci, influenza, and beta -lactamase producing bacteria, and have high stabilities to DHP-1. wherein R represents hydrogen or methyl, either one of R , R , R , or R represents the bond to the 2-position on the carbapenem ring, and the remaining three respectively represent hydrogen, halogen, nitro, cyano, alkyl, cycloalkyl, alkylthio, alkenyl, formyl, alkylcarbonyl, alkoxycarbonyl, aminosulfonyl, aryl carbonyl, aryl , carbamoyl, N-lower alkylcarbamoyl, N,N-di-lower alkylaminocarbonyl, lower alkoxyiminomethyl, or hydroxyiminomethyl, R is not present or represents alkyl, cycloalkyl, or alkenyl, and R is not present, or represents hydrogen or a group which may be metabolically hydrolyzed in the body, provided that when R is not present, R represents hydrogen or a group which may be metabolically hydrolyzed in the body, and when R is present, R is not present, and the compound forms an inner salt.
Bibliography:Application Number: AU19980056785