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Journal Abstract Search

152 related items for PubMed ID: 24594526

  • 1. 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]

  • 2. Potentiating 1-(2-hydroxypropyl)-2-styryl-5-nitroimidazole derivatives against antibacterial agents: design, synthesis and biology analysis.
    Wang ZC, Duan YT, Qin YJ, Wang PF, Luo Y, Wen Q, Yang YA, Sun J, Hu Y, Sang YL, Zhu HL.
    Eur J Med Chem; 2013 Jul 09; 65():456-63. PubMed ID: 23770447
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. 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]

  • 6. 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]

  • 7. 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 01; 7(9):1587-93. PubMed ID: 22811397
    [Abstract] [Full Text] [Related]

  • 8. Design, synthesis, and biological evaluation of chrysin derivatives as potential FabH inhibitors.
    Li HX, Wang ZC, Qian YM, Yan XQ, Lu YD, Zhu HL.
    Chem Biol Drug Des; 2017 Jan 01; 89(1):136-140. PubMed ID: 27860280
    [Abstract] [Full Text] [Related]

  • 9. Design, synthesis and biological evaluation of metronidazole-thiazole derivatives as antibacterial inhibitors.
    Qin YJ, Wang PF, Makawana JA, Wang ZC, Wang ZN, Yan-Gu, Jiang AQ, Zhu HL.
    Bioorg Med Chem Lett; 2014 Nov 15; 24(22):5279-83. PubMed ID: 25587588
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Design and synthesis of potent inhibitors of beta-ketoacyl-acyl carrier protein synthase III (FabH) as potential antibacterial agents.
    Shi L, Fang RQ, Zhu ZW, Yang Y, Cheng K, Zhong WQ, Zhu HL.
    Eur J Med Chem; 2010 Sep 21; 45(9):4358-64. PubMed ID: 20557983
    [Abstract] [Full Text] [Related]

  • 12. Design, synthesis, and structure-activity relationships of pyrazole derivatives as potential FabH inhibitors.
    Lv PC, Sun J, Luo Y, Yang Y, Zhu HL.
    Bioorg Med Chem Lett; 2010 Aug 01; 20(15):4657-60. PubMed ID: 20594840
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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 Sep 15; 17(5):474-484. PubMed ID: 31763975
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Design, synthesis and biological evaluation of novel thiazole derivatives as potent FabH inhibitors.
    Lv PC, Wang KR, Yang Y, Mao WJ, Chen J, Xiong J, Zhu HL.
    Bioorg Med Chem Lett; 2009 Dec 01; 19(23):6750-4. PubMed ID: 19836235
    [Abstract] [Full Text] [Related]

  • 17. Design, synthesis and biological evaluation of urea derivatives from o-hydroxybenzylamines and phenylisocyanate as potential FabH inhibitors.
    Li ZL, Li QS, Zhang HJ, Hu Y, Zhu DD, Zhu HL.
    Bioorg Med Chem; 2011 Aug 01; 19(15):4413-20. PubMed ID: 21752655
    [Abstract] [Full Text] [Related]

  • 18. New antibacterial agents: Hybrid bioisoster derivatives as potential E. coli FabH inhibitors.
    Segretti ND, Serafim RA, Segretti MC, Miyata M, Coelho FR, Augusto O, Ferreira EI.
    Bioorg Med Chem Lett; 2016 Aug 15; 26(16):3988-93. PubMed ID: 27426865
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Novel Schiff-base-derived FabH inhibitors with dioxygenated rings as antibiotic agents.
    Zhou Y, Du QR, Sun J, Li JR, Fang F, Li DD, Qian Y, Gong HB, Zhao J, Zhu HL.
    ChemMedChem; 2013 Mar 01; 8(3):433-41. PubMed ID: 23401291
    [Abstract] [Full Text] [Related]

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