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Volumn 45, Issue 19, 2002, Pages 4359-4370
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Inhibition of the antibacterial target UDP-(3-O-acyl)-N-acetylglucosamine deacetylase (LpxC): Isoxazoline zinc amidase inhibitors bearing diverse metal binding groups
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Author keywords
[No Author keywords available]
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Indexed keywords
3 (4 METHOXYPHENYL) 4,5 DIHYDROISOXAZOLE 5 CARBOXYLIC ACID HYDROXYAMIDE;
AMIDASE;
ANTIINFECTIVE AGENT;
ENZYME INHIBITOR;
HYDROXAMIC ACID;
ISOXAZOLINE ZINC AMIDASE INHIBITOR;
L 159692;
LIPID A;
OXAZOLINE DERIVATIVE;
UNCLASSIFIED DRUG;
URIDINE DIPHOSPHATE (3 O ACYL) N ACETYLGLUCOSAMINE DEACETYLASE;
ANTIBACTERIAL ACTIVITY;
ARTICLE;
BINDING AFFINITY;
CONTROLLED STUDY;
DRUG POTENCY;
DRUG STRUCTURE;
ENZYME ACTIVE SITE;
ENZYME INHIBITION;
ENZYME MECHANISM;
GRAM NEGATIVE BACTERIUM;
LIPOGENESIS;
METAL BINDING;
MOLECULAR STABILITY;
NONHUMAN;
TIME;
AMIDOHYDROLASES;
ANTI-BACTERIAL AGENTS;
COLONY COUNT, MICROBIAL;
ENZYME INHIBITORS;
ESCHERICHIA COLI;
HYDROXAMIC ACIDS;
INHIBITORY CONCENTRATION 50;
ISOXAZOLES;
MICROBIAL SENSITIVITY TESTS;
MODELS, MOLECULAR;
STRUCTURE-ACTIVITY RELATIONSHIP;
ZINC;
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EID: 0037068502
PISSN: 00222623
EISSN: None
Source Type: Journal
DOI: 10.1021/jm020183v Document Type: Article |
Times cited : (113)
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References (49)
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