Search Results - "Villela, Anne D"
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Is IQG-607 a Potential Metallodrug or Metallopro-Drug With a Defined Molecular Target in Mycobacterium tuberculosis ?
Published in Frontiers in microbiology (01-05-2018)“…The emergence of strains of resistant to isoniazid (INH) has underscored the need for the development of new anti-tuberculosis agents. INH is activated by the…”
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Anti-tubercular profile of new selenium-menadione conjugates against Mycobacterium tuberculosis H37Rv (ATCC 27294) strain and multidrug-resistant clinical isolates
Published in European journal of medicinal chemistry (01-01-2021)“…Tuberculosis (TB) is one of the most fatal diseases and is responsible for the infection of millions of people around the world. Most recently, scientific…”
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Nonclinical evaluation of IQG-607, an anti-tuberculosis candidate with potential use in combination drug therapy
Published in Regulatory toxicology and pharmacology (01-03-2020)“…New effective compounds to treat tuberculosis are urgently needed. IQG-607 is an orally active anti-tuberculosis drug candidate, with promising preliminary…”
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Revisiting Activation of and Mechanism of Resistance to Compound IQG-607 in Mycobacterium tuberculosis
Published in Antimicrobial agents and chemotherapy (01-02-2018)“…IQG-607 is a metal complex previously reported as a promising anti-tuberculosis (TB) drug against isoniazid (INH)-resistant strains of Unexpectedly, we found…”
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Pre-clinical evaluation of quinoxaline-derived chalcones in tuberculosis
Published in PloS one (16-08-2018)“…New effective compounds for tuberculosis treatment are needed. This study evaluated the effects of a series of quinoxaline-derived chalcones against…”
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Mefloquine and its oxazolidine derivative compound are active against drug-resistant Mycobacterium tuberculosis strains and in a murine model of tuberculosis infection
Published in International journal of antimicrobial agents (01-08-2016)“…Highlights • Mefloquine and its oxazolidine derivative 1E were active in a murine model of tuberculosis (TB). • Mefloquine and 1E were active after oral…”
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Functional, thermodynamics, structural and biological studies of in silico-identified inhibitors of Mycobacterium tuberculosis enoyl-ACP(CoA) reductase enzyme
Published in Scientific reports (24-04-2017)“…Novel chemotherapeutics agents are needed to kill Mycobacterium tuberculosis , the main causative agent of tuberculosis (TB). The M. tuberculosis 2- tran…”
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IQG-607 abrogates the synthesis of mycolic acids and displays intracellular activity against Mycobacterium tuberculosis in infected macrophages
Published in International journal of antimicrobial agents (01-01-2014)“…Abstract In this work, the antitubercular activity of a pentacyano(isoniazid)ferrate(II) compound (IQG-607) was investigated using a macrophage model of…”
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Effect of the bradykinin 1 receptor antagonist SSR240612 after oral administration in Mycobacterium tuberculosis-infected mice
Published in Tuberculosis (Edinburgh, Scotland) (01-03-2018)“…The role, if any, played by the kinin system in tuberculosis infection models, either in vivo or in vitro, was investigated. The effects of Mycobacterium…”
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Synthesis, Inhibition of Mycobacterium tuberculosis Enoyl-acyl Carrier Protein Reductase and Antimycobacterial Activity of Novel Pentacyanoferrate(II)-isonicotinoylhydrazones
Published in Journal of the Brazilian Chemical Society (01-10-2017)“…Tuberculosis remains among the top causes of death triggered by a single pathogen. Herein, a greener synthetic approach for isonicotinoylhydrazones is…”
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