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Journal Abstract Search

366 related items for PubMed ID: 23602519

  • 1. Design, synthesis and antimicrobial activities evaluation of Schiff base derived from secnidazole derivatives as potential FabH inhibitors.
    Li Y, Zhao CP, Ma HP, Zhao MY, Xue YR, Wang XM, Zhu HL.
    Bioorg Med Chem; 2013 Jun 01; 21(11):3120-6. PubMed ID: 23602519
    [Abstract] [Full Text] [Related]

  • 2. Design, synthesis and antibacterial activities of 5-(pyrazin-2-yl)-4H-1,2,4-triazole-3-thiol derivatives containing Schiff base formation as FabH inhibitory.
    Zhang F, Wen Q, Wang SF, Shahla Karim B, Yang YS, Liu JJ, Zhang WM, Zhu HL.
    Bioorg Med Chem Lett; 2014 Jan 01; 24(1):90-5. PubMed ID: 24332628
    [Abstract] [Full Text] [Related]

  • 3. Design, synthesis and antibacterial activities of vanillic acylhydrazone derivatives as potential β-ketoacyl-acyl carrier protein synthase III (FabH) inhibitors.
    Wang XL, Zhang YB, Tang JF, Yang YS, Chen RQ, Zhang F, Zhu HL.
    Eur J Med Chem; 2012 Nov 01; 57():373-82. PubMed ID: 23124163
    [Abstract] [Full Text] [Related]

  • 4. Design, synthesis and antimicrobial activities of nitroimidazole derivatives containing 1,3,4-oxadiazole scaffold as FabH inhibitors.
    Li Y, Luo Y, Hu Y, Zhu DD, Zhang S, Liu ZJ, Gong HB, Zhu HL.
    Bioorg Med Chem; 2012 Jul 15; 20(14):4316-22. PubMed ID: 22710102
    [Abstract] [Full Text] [Related]

  • 5. Synthesis, antibacterial activities and molecular docking studies of Schiff bases derived from N-(2/4-benzaldehyde-amino) phenyl-N'-phenyl-thiourea.
    Zhang HJ, Qin X, Liu K, Zhu DD, Wang XM, Zhu HL.
    Bioorg Med Chem; 2011 Sep 15; 19(18):5708-15. PubMed ID: 21872479
    [Abstract] [Full Text] [Related]

  • 6. Design and synthesis of 2-styryl of 5-Nitroimidazole derivatives and antimicrobial activities as FabH inhibitors.
    Duan YT, Wang ZC, Sang YL, Tao XX, Teraiya SB, Wang PF, Wen Q, Zhou XJ, Ding L, Yang YH, Zhu HL.
    Eur J Med Chem; 2014 Apr 09; 76():387-96. PubMed ID: 24594526
    [Abstract] [Full Text] [Related]

  • 7. Design of Arylsulfonylhydrazones as Potential FabH Inhibitors: Synthesis, Antimicrobial Evaluation and Molecular Docking.
    Fernandes TB, Segretti ND, Lourenço FR, Cândido TM, Baby AR, Barbosa EG, Parise-Filho R.
    Med Chem; 2021 Apr 09; 17(5):474-484. PubMed ID: 31763975
    [Abstract] [Full Text] [Related]

  • 8. Design and synthesis of thiazole derivatives as potent FabH inhibitors with antibacterial activity.
    Li JR, Li DD, Wang RR, Sun J, Dong JJ, Du QR, Fang F, Zhang WM, Zhu HL.
    Eur J Med Chem; 2014 Mar 21; 75():438-47. PubMed ID: 24561667
    [Abstract] [Full Text] [Related]

  • 9. Synthesis and antimicrobial activities of oximes derived from O-benzylhydroxylamine as FabH inhibitors.
    Luo Y, Zhang LR, Hu Y, Zhang S, Fu J, Wang XM, Zhu HL.
    ChemMedChem; 2012 Sep 21; 7(9):1587-93. PubMed ID: 22811397
    [Abstract] [Full Text] [Related]

  • 10. Design, synthesis and antibacterial activity studies of thiazole derivatives as potent ecKAS III inhibitors.
    Cheng K, Xue JY, Zhu HL.
    Bioorg Med Chem Lett; 2013 Jul 15; 23(14):4235-8. PubMed ID: 23731945
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  • 18. Identification of a new binding site in E. coli FabH using Molecular dynamics simulations: validation by computational alanine mutagenesis and docking studies.
    Ramamoorthy D, Turos E, Guida WC.
    J Chem Inf Model; 2013 May 24; 53(5):1138-56. PubMed ID: 23581389
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  • 20. Synthesis, molecular modeling and biological evaluation of β-ketoacyl-acyl carrier protein synthase III (FabH) as novel antibacterial agents.
    Zhang HJ, Zhu DD, Li ZL, Sun J, Zhu HL.
    Bioorg Med Chem; 2011 Aug 01; 19(15):4513-9. PubMed ID: 21741250
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