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Journal Abstract Search

248 related items for PubMed ID: 27575481

  • 1. Synthesis and biological activities of novel 5-substituted-1,3,4-oxadiazole Mannich bases and bis-Mannich bases as ketol-acid reductoisomerase inhibitors.
    Zhang Y, Liu XH, Zhan YZ, Zhang LY, Li ZM, Li YH, Zhang X, Wang BL.
    Bioorg Med Chem Lett; 2016 Oct 01; 26(19):4661-4665. PubMed ID: 27575481
    [Abstract] [Full Text] [Related]

  • 2. Synthesis, biological activities and SAR studies of new 3-substitutedphenyl-4-substitutedbenzylideneamino-1,2,4-triazole Mannich bases and bis-Mannich bases as ketol-acid reductoisomerase inhibitors.
    Wang BL, Zhang LY, Liu XH, Ma Y, Zhang Y, Li ZM, Zhang X.
    Bioorg Med Chem Lett; 2017 Dec 15; 27(24):5457-5462. PubMed ID: 29132751
    [Abstract] [Full Text] [Related]

  • 3. Synthesis and antimicrobial studies of some Mannich bases carrying imidazole moiety.
    Frank PV, Manjunatha Poojary M, Damodara N, Chikkanna C.
    Acta Pharm; 2013 Jun 15; 63(2):231-9. PubMed ID: 23846145
    [Abstract] [Full Text] [Related]

  • 4. Synthesis and biological activity of some novel trifluoromethyl-substituted 1,2,4-triazole and bis(1,2,4-triazole) Mannich bases containing piperazine rings.
    Wang BL, Shi YX, Ma Y, Liu XH, Li YH, Song HB, Li BJ, Li ZM.
    J Agric Food Chem; 2010 May 12; 58(9):5515-22. PubMed ID: 20384340
    [Abstract] [Full Text] [Related]

  • 5. High throughput receptor-based virtual screening under ZINC database, synthesis, and biological evaluation of ketol-acid reductoisomerase inhibitors.
    Liu XH, Chen PQ, Wang BL, Dong WL, Li YH, Xie XQ, Li ZM.
    Chem Biol Drug Des; 2010 Feb 12; 75(2):228-32. PubMed ID: 20028400
    [Abstract] [Full Text] [Related]

  • 6. Synthesis, structure, and biological activity of novel (oxdi/tri)azoles derivatives containing 1,2,3-thiadiazole or methyl moiety.
    Liu XH, Pan L, Weng JQ, Tan CX, Li YH, Wang BL, Li ZM.
    Mol Divers; 2012 May 12; 16(2):251-60. PubMed ID: 22249419
    [Abstract] [Full Text] [Related]

  • 7. Synthesis, bioactivity and SAR study of N'-(5-substituted-1,3,4-thiadiazol-2-yl)-N-cyclopropylformyl-thioureas as ketol-acid reductoisomerase inhibitors.
    Liu XH, Zhang CY, Guo WC, Li YH, Chen PQ, Wang T, Dong WL, Wang BL, Sun HW, Li ZM.
    J Enzyme Inhib Med Chem; 2009 Apr 12; 24(2):545-52. PubMed ID: 18763167
    [Abstract] [Full Text] [Related]

  • 8. Oxadiazole mannich bases: synthesis and antimycobacterial activity.
    Ali MA, Shaharyar M.
    Bioorg Med Chem Lett; 2007 Jun 15; 17(12):3314-6. PubMed ID: 17467984
    [Abstract] [Full Text] [Related]

  • 9. Synthesis, bioactivity, theoretical and molecular docking study of 1-cyano-N-substituted-cyclopropanecarboxamide as ketol-acid reductoisomerase inhibitor.
    Liu XH, Chen PQ, Wang BL, Li YH, Wang SH, Li ZM.
    Bioorg Med Chem Lett; 2007 Jul 01; 17(13):3784-8. PubMed ID: 17512731
    [Abstract] [Full Text] [Related]

  • 10. 1,3,4-Oxadiazole N-Mannich Bases: Synthesis, Antimicrobial, and Anti-Proliferative Activities.
    Al-Wahaibi LH, Mohamed AAB, Tawfik SS, Hassan HM, El-Emam AA.
    Molecules; 2021 Apr 07; 26(8):. PubMed ID: 33916955
    [Abstract] [Full Text] [Related]

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  • 12. Synthesis, structure and biological activity of novel 1,2,4-triazole mannich bases containing a substituted benzylpiperazine moiety.
    Wang BL, Liu XH, Zhang XL, Zhang JF, Song HB, Li ZM.
    Chem Biol Drug Des; 2011 Jul 07; 78(1):42-9. PubMed ID: 21521489
    [Abstract] [Full Text] [Related]

  • 13. Synthesis, anti-inflammatory activity, and molecular docking studies of some novel Mannich bases of the 1,3,4-oxadiazole-2(3H)-thione scaffold.
    Ozyazici T, Gurdal EE, Orak D, Sipahi H, Ercetin T, Gulcan HO, Koksal M.
    Arch Pharm (Weinheim); 2020 Jul 07; 353(7):e2000061. PubMed ID: 32319141
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  • 15. Design, Synthesis, Characterization and Computational Studies of Mannich Bases Oxadiazole Derivatives as New Class of Jack Bean Urease Inhibitors.
    Mutahir S, Khan MA, Almehizia AA, Abouzied AS, Khalifa NE, Naglah AM, Deng H, Refat MS, Khojali WMA, Huwaimel B.
    Chem Biodivers; 2023 Aug 07; 20(8):e202300241. PubMed ID: 37344354
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  • 17. Crystal structure of Mycobacterium tuberculosis ketol-acid reductoisomerase at 1.0 Å resolution - a potential target for anti-tuberculosis drug discovery.
    Lv Y, Kandale A, Wun SJ, McGeary RP, Williams SJ, Kobe B, Sieber V, Schembri MA, Schenk G, Guddat LW.
    FEBS J; 2016 Apr 07; 283(7):1184-96. PubMed ID: 26876563
    [Abstract] [Full Text] [Related]

  • 18. Discovery and evaluation of novel Mycobacterium tuberculosis ketol-acid reductoisomerase inhibitors as therapeutic drug leads.
    Krishna VS, Zheng S, Rekha EM, Guddat LW, Sriram D.
    J Comput Aided Mol Des; 2019 Mar 07; 33(3):357-366. PubMed ID: 30666485
    [Abstract] [Full Text] [Related]

  • 19. Synthesis and antioxidant activity of novel Mannich base of 1,3,4-oxadiazole derivatives possessing 1,4-benzodioxan.
    Ma L, Xiao Y, Li C, Xie ZL, Li DD, Wang YT, Ma HT, Zhu HL, Wang MH, Ye YH.
    Bioorg Med Chem; 2013 Nov 01; 21(21):6763-70. PubMed ID: 23993673
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