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...
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Main Authors | , , , , , , , , , |
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Format | Patent |
Language | English |
Published |
22.03.2001
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Edition | 6 |
Subjects | |
Online Access | Get full text |
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Abstract | 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. |
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AbstractList | 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. |
Author | YUKO KANO KAZUKO KOBAYASHI KUNIO ATSUMI KATSUYOSHI IWAMATSU KAZUHIRO AIHARA TAKASHI IDA TOSHIRO SASAKI KENICHI FUSHIHARA HIROMASA TAKIZAWA YUMIKO TOYOOKA |
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Snippet | The carbapenem derivatives represented by the following formula (I) is disclosed. These compounds have strong anti-bacterial activities against bacteria... |
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Title | New carbapenem derivatives |
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