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New Classes of Alanine Racemase Inhibitors Identified by High-Throughput Screening Show Antimicrobial Activity against Mycobacterium tuberculosis
by
Anthony, Karen G.
, Krause, Kurt L.
, Shoen, Carolyn S.
, Strych, Ulrich
, Cynamon, Michael H.
, Aristoff, Paul A.
, Perez, Oriana
, Yeung, Kacheong R.
, Koski, Raymond A.
in
Alanine
/ Alanine Dehydrogenase - metabolism
/ Alanine racemase
/ Alanine Racemase - antagonists & inhibitors
/ Alanine Racemase - chemistry
/ Alanine Racemase - metabolism
/ Alanine Racemase - pharmacology
/ Amino acids
/ Analogs
/ Anti-Infective Agents - analysis
/ Anti-Infective Agents - chemistry
/ Anti-Infective Agents - classification
/ Anti-Infective Agents - pharmacology
/ Antiinfectives and antibacterials
/ Antimicrobial activity
/ Antimicrobial agents
/ Biochemistry
/ Biology
/ Biosynthesis
/ Cell Death - drug effects
/ Cell walls
/ Cells (Biology)
/ Cellular structure
/ Cytotoxicity
/ D-Alanine
/ Dehydrogenases
/ Drug discovery
/ Drugs
/ Enzyme inhibitors
/ Enzyme Inhibitors - analysis
/ Enzyme Inhibitors - chemistry
/ Enzyme Inhibitors - classification
/ Enzyme Inhibitors - pharmacology
/ Enzymes
/ Feasibility studies
/ HeLa Cells
/ High-throughput screening
/ High-Throughput Screening Assays - methods
/ Humans
/ Inhibitors
/ Inhibitory Concentration 50
/ Kinetics
/ L-Alanine
/ Lead compounds
/ Mammalian cells
/ Mass Spectrometry
/ Medicine
/ Microbial Sensitivity Tests
/ Mycobacterium tuberculosis - drug effects
/ Peptidoglycans
/ Permeability
/ Salmonella
/ Salmonella Typhimurium
/ Screening
/ Substrate inhibition
/ Substrate Specificity - drug effects
/ Substrates
/ Suicide
/ Suicide substrates
/ Toxicity
/ Tuberculosis
2011
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New Classes of Alanine Racemase Inhibitors Identified by High-Throughput Screening Show Antimicrobial Activity against Mycobacterium tuberculosis
by
Anthony, Karen G.
, Krause, Kurt L.
, Shoen, Carolyn S.
, Strych, Ulrich
, Cynamon, Michael H.
, Aristoff, Paul A.
, Perez, Oriana
, Yeung, Kacheong R.
, Koski, Raymond A.
in
Alanine
/ Alanine Dehydrogenase - metabolism
/ Alanine racemase
/ Alanine Racemase - antagonists & inhibitors
/ Alanine Racemase - chemistry
/ Alanine Racemase - metabolism
/ Alanine Racemase - pharmacology
/ Amino acids
/ Analogs
/ Anti-Infective Agents - analysis
/ Anti-Infective Agents - chemistry
/ Anti-Infective Agents - classification
/ Anti-Infective Agents - pharmacology
/ Antiinfectives and antibacterials
/ Antimicrobial activity
/ Antimicrobial agents
/ Biochemistry
/ Biology
/ Biosynthesis
/ Cell Death - drug effects
/ Cell walls
/ Cells (Biology)
/ Cellular structure
/ Cytotoxicity
/ D-Alanine
/ Dehydrogenases
/ Drug discovery
/ Drugs
/ Enzyme inhibitors
/ Enzyme Inhibitors - analysis
/ Enzyme Inhibitors - chemistry
/ Enzyme Inhibitors - classification
/ Enzyme Inhibitors - pharmacology
/ Enzymes
/ Feasibility studies
/ HeLa Cells
/ High-throughput screening
/ High-Throughput Screening Assays - methods
/ Humans
/ Inhibitors
/ Inhibitory Concentration 50
/ Kinetics
/ L-Alanine
/ Lead compounds
/ Mammalian cells
/ Mass Spectrometry
/ Medicine
/ Microbial Sensitivity Tests
/ Mycobacterium tuberculosis - drug effects
/ Peptidoglycans
/ Permeability
/ Salmonella
/ Salmonella Typhimurium
/ Screening
/ Substrate inhibition
/ Substrate Specificity - drug effects
/ Substrates
/ Suicide
/ Suicide substrates
/ Toxicity
/ Tuberculosis
2011
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New Classes of Alanine Racemase Inhibitors Identified by High-Throughput Screening Show Antimicrobial Activity against Mycobacterium tuberculosis
by
Anthony, Karen G.
, Krause, Kurt L.
, Shoen, Carolyn S.
, Strych, Ulrich
, Cynamon, Michael H.
, Aristoff, Paul A.
, Perez, Oriana
, Yeung, Kacheong R.
, Koski, Raymond A.
in
Alanine
/ Alanine Dehydrogenase - metabolism
/ Alanine racemase
/ Alanine Racemase - antagonists & inhibitors
/ Alanine Racemase - chemistry
/ Alanine Racemase - metabolism
/ Alanine Racemase - pharmacology
/ Amino acids
/ Analogs
/ Anti-Infective Agents - analysis
/ Anti-Infective Agents - chemistry
/ Anti-Infective Agents - classification
/ Anti-Infective Agents - pharmacology
/ Antiinfectives and antibacterials
/ Antimicrobial activity
/ Antimicrobial agents
/ Biochemistry
/ Biology
/ Biosynthesis
/ Cell Death - drug effects
/ Cell walls
/ Cells (Biology)
/ Cellular structure
/ Cytotoxicity
/ D-Alanine
/ Dehydrogenases
/ Drug discovery
/ Drugs
/ Enzyme inhibitors
/ Enzyme Inhibitors - analysis
/ Enzyme Inhibitors - chemistry
/ Enzyme Inhibitors - classification
/ Enzyme Inhibitors - pharmacology
/ Enzymes
/ Feasibility studies
/ HeLa Cells
/ High-throughput screening
/ High-Throughput Screening Assays - methods
/ Humans
/ Inhibitors
/ Inhibitory Concentration 50
/ Kinetics
/ L-Alanine
/ Lead compounds
/ Mammalian cells
/ Mass Spectrometry
/ Medicine
/ Microbial Sensitivity Tests
/ Mycobacterium tuberculosis - drug effects
/ Peptidoglycans
/ Permeability
/ Salmonella
/ Salmonella Typhimurium
/ Screening
/ Substrate inhibition
/ Substrate Specificity - drug effects
/ Substrates
/ Suicide
/ Suicide substrates
/ Toxicity
/ Tuberculosis
2011
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New Classes of Alanine Racemase Inhibitors Identified by High-Throughput Screening Show Antimicrobial Activity against Mycobacterium tuberculosis
Journal Article
New Classes of Alanine Racemase Inhibitors Identified by High-Throughput Screening Show Antimicrobial Activity against Mycobacterium tuberculosis
2011
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Overview
In an effort to discover new drugs to treat tuberculosis (TB) we chose alanine racemase as the target of our drug discovery efforts. In Mycobacterium tuberculosis, the causative agent of TB, alanine racemase plays an essential role in cell wall synthesis as it racemizes L-alanine into D-alanine, a key building block in the biosynthesis of peptidoglycan. Good antimicrobial effects have been achieved by inhibition of this enzyme with suicide substrates, but the clinical utility of this class of inhibitors is limited due to their lack of target specificity and toxicity. Therefore, inhibitors that are not substrate analogs and that act through different mechanisms of enzyme inhibition are necessary for therapeutic development for this drug target.
To obtain non-substrate alanine racemase inhibitors, we developed a high-throughput screening platform and screened 53,000 small molecule compounds for enzyme-specific inhibitors. We examined the 'hits' for structural novelty, antimicrobial activity against M. tuberculosis, general cellular cytotoxicity, and mechanism of enzyme inhibition. We identified seventeen novel non-substrate alanine racemase inhibitors that are structurally different than any currently known enzyme inhibitors. Seven of these are active against M. tuberculosis and minimally cytotoxic against mammalian cells.
This study highlights the feasibility of obtaining novel alanine racemase inhibitor lead compounds by high-throughput screening for development of new anti-TB agents.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Alanine Dehydrogenase - metabolism
/ Alanine Racemase - antagonists & inhibitors
/ Alanine Racemase - chemistry
/ Alanine Racemase - metabolism
/ Alanine Racemase - pharmacology
/ Analogs
/ Anti-Infective Agents - analysis
/ Anti-Infective Agents - chemistry
/ Anti-Infective Agents - classification
/ Anti-Infective Agents - pharmacology
/ Antiinfectives and antibacterials
/ Biology
/ Drugs
/ Enzyme Inhibitors - analysis
/ Enzyme Inhibitors - chemistry
/ Enzyme Inhibitors - classification
/ Enzyme Inhibitors - pharmacology
/ Enzymes
/ High-Throughput Screening Assays - methods
/ Humans
/ Kinetics
/ Medicine
/ Mycobacterium tuberculosis - drug effects
/ Substrate Specificity - drug effects
/ Suicide
/ Toxicity
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