The structure-activity relationship of urea derivatives as anti-tuberculosis agents.
about
New agents for the treatment of drug-resistant Mycobacterium tuberculosisActivities of N,N'-Diarylurea MMV665852 analogs against Schistosoma mansoniInhibition of mycolic acid transport across the Mycobacterium tuberculosis plasma membraneCopper complexation screen reveals compounds with potent antibiotic properties against methicillin-resistant Staphylococcus aureus.Screening a library of 1600 adamantyl ureas for anti-Mycobacterium tuberculosis activity in vitro and for better physical chemical properties for bioavailability.Covalent modification of the Mycobacterium tuberculosis FAS-II dehydratase by Isoxyl and Thiacetazone.The tuberculosis drug discovery and development pipeline and emerging drug targets.New approaches to target the mycolic acid biosynthesis pathway for the development of tuberculosis therapeutics.A common mechanism of inhibition of the Mycobacterium tuberculosis mycolic acid biosynthetic pathway by isoxyl and thiacetazoneAntiinfectives targeting enzymes and the proton motive force.Advances in Drug Discovery and Development for Pediatric Tuberculosis.Design, synthesis and anti-tuberculosis activity of 1-adamantyl-3-heteroaryl ureas with improved in vitro pharmacokinetic properties.Therapeutic Potential of the Mycobacterium tuberculosis Mycolic Acid Transporter, MmpL3Insights on how the Mycobacterium tuberculosis heme uptake pathway can be used as a drug target.Progress in targeting cell envelope biogenesis in Mycobacterium tuberculosis.Synergistic Interactions of MmpL3 Inhibitors with Antitubercular Compounds In Vitro.Resistance in tuberculosis: what do we know and where can we go?Tuberculosis drug discovery and emerging targets.Design, synthesis and evaluation of indole-2-carboxamides with pan anti-mycobacterial activity.New structural classes of antituberculosis agents.Synthesis, antimicrobial, and anti-inflammatory activity, of novel S-substituted and N-substituted 5-(1-adamantyl)-1,2,4-triazole-3-thiols.Novel Sulfamethoxazole Ureas and Oxalamide as Potential Antimycobacterial Agents.Solvent-free synthesis, DNA-topoisomerase II activity and molecular docking study of new asymmetrically N,N'-substituted ureas.
P2860
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P2860
The structure-activity relationship of urea derivatives as anti-tuberculosis agents.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
The structure-activity relationship of urea derivatives as anti-tuberculosis agents.
@ast
The structure-activity relationship of urea derivatives as anti-tuberculosis agents.
@en
type
label
The structure-activity relationship of urea derivatives as anti-tuberculosis agents.
@ast
The structure-activity relationship of urea derivatives as anti-tuberculosis agents.
@en
prefLabel
The structure-activity relationship of urea derivatives as anti-tuberculosis agents.
@ast
The structure-activity relationship of urea derivatives as anti-tuberculosis agents.
@en
P2093
P2860
P50
P1476
The structure-activity relationship of urea derivatives as anti-tuberculosis agents.
@en
P2093
Anna Grzegorzewicz
Christophe Morisseau
Dianqing Sun
Elton J North
Jerrod S Scarborough
Joshua R Brown
Julian G Hurdle
Michael R McNeil
Michael S Scherman
Rebecca M Crew
P2860
P304
P356
10.1016/J.BMC.2011.07.034
P407
P577
2011-07-24T00:00:00Z