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Volumn 343, Issue 3, 2010, Pages 143-151
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Synthesis and in vitro antibacterial activity of 7-(3-alkoxyimino-4-methyl- 4-methylaminopiperidin-1-yl)-fluoroquinolone derivatives
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Author keywords
Antibacterial activity; Fluoroquinolone; Synthesis
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Indexed keywords
1 (2 FLUOROETHYL) 6,8 DIFLUORO 7 (3 ETHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXOQUINOLINE 3 CARBOXYLIC ACID;
1 (2 FLUOROETHYL) 6,8 DIFLUORO 7 (3 METHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXOQUINOLINE 3 CARBOXYLIC ACID;
1 (2,4 DIFLUOROPHENYL) 6 FLUORO 7 (3 ETHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO 1,8 NAPHTHYRIDINE 3 CARBOXYLIC ACID;
1 (2,4 DIFLUOROPHENYL) 6 FLUORO 7 (3 METHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO 1,8 NAPHTHYRIDINE 3 CARBOXYLIC ACID;
1 CYCLOPROPYL 6 FLUORO 7 (3 ETHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO 1,8 NAPHTHYRIDIN 3 CARBOXYLIC ACID;
1 CYCLOPROPYL 6 FLUORO 7 (3 ETHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO QUINOLINE 3 CARBOXYLIC ACID;
1 CYCLOPROPYL 6 FLUORO 7 (3 ETHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 8 METHOXYL 1,4 DIHYDRO 4 OXO QUINOLINE 3 CARBOXYLIC ACID;
1 CYCLOPROPYL 6 FLUORO 7 (3 METHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO 1,8 NAPHTHYRIDINE 3 CARBOXYLIC ACID;
1 CYCLOPROPYL 6 FLUORO 7 (3 METHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO QUINOLINE 3 CARBOXYLIC ACID;
1 CYCLOPROPYL 6 FLUORO 7 (3 METHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 8 METHOXYL 1,4 DIHYDRO 4 OXO QUINOLINE 3 CARBOXYLIC ACID;
1 CYCLOPROPYL 6,8 DIFLUORO 7 (3 ETHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO QUINOLINE 3 CARBOXYLIC ACID;
1 ETHYL 6 FLUORO 7 (3 ETHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO QUINOLINE 3 CARBOXYLIC ACID;
1 ETHYL 6 FLUORO 7 (3 METHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO QUINOLINE 3 CARBOXYLIC ACID;
1 ETHYL 6,8 DIFLUORO 7 (3 METHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 1,4 DIHYDRO 4 OXO QUINOLINE 3 CARBOXYLIC ACID;
7 (3 ALKOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL)FLUOROQUINOLONE DERIVATIVE;
9 FLUORO 3 METHYL 10 (3 ETHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 7 OXO 2,3 DIHYDRO 7H PYRRIDO[1,2,3 D,E][1,4]BENZOXAZINE 6 CARBOXYLIC ACID;
9 FLUORO 3 METHYL 10 (3 METHOXYIMINO 4 METHYL 4 METHYLAMINOPIPERIDIN 1 YL) 7 OXO 2,3 DIHYDRO 7H PYRRIDO[1,2,3 D,E][1,4]BENZOXAZINE 6 CARBOXYLIC ACID;
ANTIINFECTIVE AGENT;
CIPROFLOXACIN;
GEMIFLOXACIN;
LEVOFLOXACIN;
UNCLASSIFIED DRUG;
ACINETOBACTER CALCOACETICUS;
ANTIBACTERIAL ACTIVITY;
ARTICLE;
BACTERIAL STRAIN;
CONTROLLED STUDY;
DRUG ACTIVITY;
DRUG DESIGN;
DRUG STRUCTURE;
DRUG SYNTHESIS;
IN VITRO STUDY;
METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS;
NONHUMAN;
NUCLEAR MAGNETIC RESONANCE;
PRIORITY JOURNAL;
ANTI-BACTERIAL AGENTS;
CHEMISTRY, PHARMACEUTICAL;
CIPROFLOXACIN;
FLUOROQUINOLONES;
MICROBIAL SENSITIVITY TESTS;
MOLECULAR STRUCTURE;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 77949379146
PISSN: 03656233
EISSN: 15214184
Source Type: Journal
DOI: 10.1002/ardp.200900191 Document Type: Article |
Times cited : (21)
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References (25)
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