Molecular cloning, characterization, and inhibition studies of the Rv1284 beta-carbonic anhydrase from Mycobacterium tuberculosis with sulfonamides and a sulfamate
about
A class of carbonic anhydrase I - selective activators.Characterization of the first beta-class carbonic anhydrase from an arthropod (Drosophila melanogaster) and phylogenetic analysis of beta-class carbonic anhydrases in invertebratesCarbonic anhydrase is essential for Streptococcus pneumoniae growth in environmental ambient air.Biochemistry and physiology of the β class carbonic anhydrase (Cpb) from Clostridium perfringens strain 13Heterocyclic urea derivatives and methods of use thereof (WO2010142978).Carbonic anhydrase inhibitors and activators for novel therapeutic applications.Structure-based drug discovery of carbonic anhydrase inhibitors.Anti-infective carbonic anhydrase inhibitors: a patent and literature review.Bacterial, fungal and protozoan carbonic anhydrases as drug targets.How many carbonic anhydrase inhibition mechanisms exist?Inhibition of carbonic anhydrase from Trypanosoma cruzi for the management of Chagas disease: an underexplored therapeutic opportunity.Small Molecules That Sabotage Bacterial Virulence.New structural classes of antituberculosis agents.Quinazoline-sulfonamides as potential antitumor agents: synthesis and biological testing.Microbial Carbonic Anhydrases in Biomimetic Carbon Sequestration for Mitigating Global Warming: Prospects and Perspectives.Bacterial carbonic anhydrases as drug targets: toward novel antibiotics?Hydrophobic substituents of the phenylmethylsulfamide moiety can be used for the development of new selective carbonic anhydrase inhibitors.Dithiocarbamates strongly inhibit the β-class carbonic anhydrases from Mycobacterium tuberculosis.Inhibition of the β-class carbonic anhydrases from Mycobacterium tuberculosis with carboxylic acids.Cloning, expression and biochemical characterization of a β-carbonic anhydrase from the soil bacterium Enterobacter sp. B13.The working mechanism of the β-carbonic anhydrase degrading carbonyl sulphide (COSase): a theoretical study.Sulfonamides incorporating fluorine and 1,3,5-triazine moieties are effective inhibitors of three β-class carbonic anhydrases from Mycobacterium tuberculosis.Non-classical β-carbonic anhydrase inhibitors-towards novel anti-mycobacterialsDihalogenated sulfanilamides and benzolamides are effective inhibitors of the three β-class carbonic anhydrases fromMycobacterium tuberculosis
P2860
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P2860
Molecular cloning, characterization, and inhibition studies of the Rv1284 beta-carbonic anhydrase from Mycobacterium tuberculosis with sulfonamides and a sulfamate
description
2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2009
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im April 2009 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 2009/04/23)
@sk
vědecký článek publikovaný v roce 2009
@cs
wetenschappelijk artikel (gepubliceerd op 2009/04/23)
@nl
наукова стаття, опублікована у квітні 2009
@uk
مقالة علمية (نشرت في 23-4-2009)
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name
Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
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Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
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Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
@nl
type
label
Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
@ast
Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
@en
Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
@nl
prefLabel
Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
@ast
Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
@en
Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
@nl
P2093
P356
P1476
Molecular cloning, characteriz ...... h sulfonamides and a sulfamate
@en
P2093
Claudiu T. Supuran
Daniela Vullo
Isao Nishimori
Tomoko Minakuchi
P304
P356
10.1021/JM9000488
P407
P577
2009-04-23T00:00:00Z