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Generation and exploration of new classes of antitubercular agents: The optimization of oxazolines, oxazoles, thiazolines, thiazoles to imidazo[1,2-a]pyridines and isomeric 5,6-fused scaffolds

https://doi.org/10.1016/j.bmc.2012.02.025
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/j.bmcl.2009.06.045openalex-snapshot
Functionalized 3-amino-imidazo[1,2-a]pyridines: A novel class of drug-like Mycobacterium tuberculosis glutamine synthetase inhibitors
inferredcites →https://doi.org/10.1016/j.ejmech.2009.12.074openalex-snapshot
Structure–activity relationship of new anti-tuberculosis agents derived from oxazoline and oxazole benzyl esters
inferredcites →https://doi.org/10.1016/j.ejmech.2010.09.049openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4039(96)02344-1openalex-snapshot
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inferredcites →https://doi.org/10.1016/s1351-4180(03)00541-5openalex-snapshot
Chiral Quest receives US patent for ferrocene amide phosphine
inferredcites →https://doi.org/10.1021/jm901273nopenalex-snapshot
Rational Design of 5-Phenyl-3-isoxazolecarboxylic Acid Ethyl Esters as Growth Inhibitors of Mycobacterium tuberculosis. A Potent and Selective Series for Further Drug Development
inferredcites →https://doi.org/10.1021/ml200036ropenalex-snapshot
Advent of Imidazo[1,2-a]pyridine-3-carboxamides with Potent Multi- and Extended Drug Resistant Antituberculosis Activity
inferredcites →https://doi.org/10.1021/ol005777bopenalex-snapshot
Synthesis of Functionalized Oxazolines and Oxazoles with DAST and Deoxo-Fluor
inferredcites →https://doi.org/10.1038/35016103openalex-snapshot
A small-molecule nitroimidazopyran drug candidate for the treatment of tuberculosis
inferredcites →https://doi.org/10.1038/ncomms1060openalex-snapshot
A chemical genetic screen in Mycobacterium tuberculosis identifies carbon-source-dependent growth inhibitors devoid of in vivo efficacy
inferredcites →https://doi.org/10.1038/nrmicro1816openalex-snapshot
Drugs versus bugs: in pursuit of the persistent predator Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1039/b612475eopenalex-snapshot
New C-3′ hydroxamate-substituted and more lipophilic cyclic hydroxamate cephalosporin derivatives as a potential new generation of selective antimicrobial agents
inferredcites →https://doi.org/10.1073/pnas.0508392103openalex-snapshot
Identification of a nitroimidazo-oxazine-specific protein involved in PA-824 resistance in Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1073/pnas.97.3.1252openalex-snapshot
The salicylate-derived mycobactin siderophores of Mycobacterium tuberculosis are essential for growth in macrophages
inferredcites →https://doi.org/10.1084/jem.189.9.1425openalex-snapshot
An Inhibitor of Exported Mycobacterium tuberculosis Glutamine Synthetase Selectively Blocks the Growth of Pathogenic Mycobacteria in Axenic Culture and in Human Monocytes: Extracellular Proteins as Potential Novel Drug Targets
inferredcites →https://doi.org/10.1111/j.1753-6405.2012.00928.xopenalex-snapshot
Global Tuberculosis Control: WHO Report 2011
inferredcites →https://doi.org/10.1128/aac.00055-06openalex-snapshot
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inferredcites →https://doi.org/10.1128/aac.36.4.840openalex-snapshot
Iron transport-mediated antibacterial activity of and development of resistance to hydroxamate and catechol siderophore-carbacephalosporin conjugates
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inferredcites →https://doi.org/10.1201/b15569-15openalex-snapshot
The United States Pharmacopeia/National Formulary
inferredcites →https://doi.org/10.3233/wor-1997-8111openalex-snapshot
Tuberculosis: a global emergency
inferredcites →https://doi.org/10.3987/com-09-s(s)69openalex-snapshot
Utilization of the Suzuki Coupling to Enhance the Antituberculosis Activity of Aryloxazoles

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Suffocating tuberculosis : oxidative phosphorylation as a target space for the development of next generation anti-tuberculosis drugs
inferred← citeshttps://doi.org/10.3390/biomedicines12010213openalex-snapshot
Selenium-Containing (Hetero)Aryl Hybrids as Potential Antileishmanial Drug Candidates: In Vitro Screening against L. amazonensis
inferred← citeshttps://doi.org/10.3390/molecules21010049openalex-snapshot
Design, Synthesis and Antimycobacterial Activity of Novel Imidazo[1,2-a]pyridine Amide-Cinnamamide Hybrids
inferred← citeshttps://doi.org/10.3390/molecules23030599openalex-snapshot
Synthesis, Molecular Docking, and Antimycotic Evaluation of Some 3-Acyl Imidazo[1,2-a]pyrimidines
inferred← citeshttps://doi.org/10.3390/molecules27196321openalex-snapshot
A Review on the Synthesis of Fluorescent Five- and Six-Membered Ring Azaheterocycles
inferred← citeshttps://doi.org/10.3390/ph15040388openalex-snapshot
On the Hunt for Next-Generation Antimicrobial Agents: An Online Symposium Organized Jointly by the French Society for Medicinal Chemistry (Société de Chimie Thérapeutique) and the French Microbiology Society (Société Française de Microbiologie) on 9–10 December 2021
inferred← citeshttps://doi.org/10.3762/bjoc.20.238openalex-snapshot
Synthesis of tricarbonylated propargylamine and conversion to 2,5-disubstituted oxazole-4-carboxylates
inferred← citeshttps://doi.org/10.3987/com-15-13299openalex-snapshot
Microwave Assisted Synthesis of Disubstituted Imidazo[1,2-a]pyridine-3-carboxylic Acid Esters
inferred← citeshttps://doi.org/10.4172/2471-9315.1000122openalex-snapshot
A Brief Overview on Recent Advances in the Development of Anti-Tubercular Compounds Containing Different Heterocyclic Ring Systems
inferred← citeshttps://doi.org/10.5897/ajb12.2649openalex-snapshot
In vitro antifungal activity of Argemone ochroleuca Sweet latex against some pathogenic fungi
inferred← citeshttps://doi.org/10.59049/2790-0231.10.2.2308openalex-snapshot
Targeting Drug-Resistant Bacteria: The Promise of Oxazole-Based Antibacterial Agents and their structure-activity relationships (SAR): Review
inferred← citeshttps://doi.org/10.70675/6f1169d5z0f99z428ez8ddbz62fac9faebecopenalex-snapshot
Nouveaux matériaux donneur-π-accepteur transporteurs de trous pour cellules solaires pérovskites
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