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Journal Abstract Search

530 related items for PubMed ID: 21944473

  • 1.
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  • 2. Chemical synthesis and biological evaluation of triazole derivatives as inhibitors of InhA and antituberculosis agents.
    Menendez C, Chollet A, Rodriguez F, Inard C, Pasca MR, Lherbet C, Baltas M.
    Eur J Med Chem; 2012 Jun; 52():275-83. PubMed ID: 22483635
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  • 4. First triclosan-based macrocyclic inhibitors of InhA enzyme.
    Rodriguez F, Saffon N, Sammartino JC, Degiacomi G, Pasca MR, Lherbet C.
    Bioorg Chem; 2020 Jan; 95():103498. PubMed ID: 31855823
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  • 5. Efficient synthesis and in vitro antitubercular activity of 1,2,3-triazoles as inhibitors of Mycobacterium tuberculosis.
    Shanmugavelan P, Nagarajan S, Sathishkumar M, Ponnuswamy A, Yogeeswari P, Sriram D.
    Bioorg Med Chem Lett; 2011 Dec 15; 21(24):7273-6. PubMed ID: 22061642
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  • 7. High affinity InhA inhibitors with activity against drug-resistant strains of Mycobacterium tuberculosis.
    Sullivan TJ, Truglio JJ, Boyne ME, Novichenok P, Zhang X, Stratton CF, Li HJ, Kaur T, Amin A, Johnson F, Slayden RA, Kisker C, Tonge PJ.
    ACS Chem Biol; 2006 Feb 17; 1(1):43-53. PubMed ID: 17163639
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  • 8. Inhibition of Mycobacterium tuberculosis InhA: Design, synthesis and evaluation of new di-triclosan derivatives.
    Armstrong T, Lamont M, Lanne A, Alderwick LJ, Thomas NR.
    Bioorg Med Chem; 2020 Nov 15; 28(22):115744. PubMed ID: 33007556
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  • 9. Application of Huisgen (3+2) cycloaddition reaction: synthesis of 1-(2,3-dihydrobenzofuran-2-yl-methyl [1,2,3]-triazoles and their antitubercular evaluations.
    Tripathi RP, Yadav AK, Ajay A, Bisht SS, Chaturvedi V, Sinha SK.
    Eur J Med Chem; 2010 Jan 15; 45(1):142-8. PubMed ID: 19846238
    [Abstract] [Full Text] [Related]

  • 10. Biological evaluation of potent triclosan-derived inhibitors of the enoyl-acyl carrier protein reductase InhA in drug-sensitive and drug-resistant strains of Mycobacterium tuberculosis.
    Stec J, Vilchèze C, Lun S, Perryman AL, Wang X, Freundlich JS, Bishai W, Jacobs WR, Kozikowski AP.
    ChemMedChem; 2014 Nov 15; 9(11):2528-37. PubMed ID: 25165007
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  • 12. Synthesis of 3-heteryl substituted pyrrolidine-2,5-diones via catalytic Michael reaction and evaluation of their inhibitory activity against InhA and Mycobacterium tuberculosis.
    Matviiuk T, Mori G, Lherbet C, Rodriguez F, Pasca MR, Gorichko M, Guidetti B, Voitenko Z, Baltas M.
    Eur J Med Chem; 2014 Jan 15; 71():46-52. PubMed ID: 24269516
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  • 15. Chemical synthesis and in silico molecular modeling of novel pyrrolyl benzohydrazide derivatives: Their biological evaluation against enoyl ACP reductase (InhA) and Mycobacterium tuberculosis.
    Joshi SD, More UA, Dixit SR, Balmi SV, Kulkarni BG, Ullagaddi G, Lherbet C, Aminabhavi TM.
    Bioorg Chem; 2017 Dec 15; 75():181-200. PubMed ID: 28961440
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  • 16. New coumarin linked thiazole derivatives as antimycobacterial agents: Design, synthesis, enoyl acyl carrier protein reductase (InhA) inhibition and molecular modeling.
    Kassem AF, Sabt A, Korycka-Machala M, Shaldam MA, Kawka M, Dziadek B, Kuzioła M, Dziadek J, Batran RZ.
    Bioorg Chem; 2024 Sep 15; 150():107511. PubMed ID: 38870705
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  • 18. Synthesis of quinoline coupled [1,2,3]-triazoles as a promising class of anti-tuberculosis agents.
    Karthik Kumar K, Prabu Seenivasan S, Kumar V, Mohan Das T.
    Carbohydr Res; 2011 Oct 18; 346(14):2084-90. PubMed ID: 21767828
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