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Journal Abstract Search

841 related items for PubMed ID: 29084182

  • 1. Synthesis, Biological Evaluation and Molecular Docking Study of 2-Substituted-4,6-Diarylpyrimidines as α-Glucosidase Inhibitors.
    Gong Z, Xie Z, Qiu J, Wang G.
    Molecules; 2017 Oct 30; 22(11):. PubMed ID: 29084182
    [Abstract] [Full Text] [Related]

  • 2. Synthesis, in vitro α-glucosidase inhibitory activity and docking studies of novel chromone-isatin derivatives.
    Wang G, Chen M, Qiu J, Xie Z, Cao A.
    Bioorg Med Chem Lett; 2018 Jan 15; 28(2):113-116. PubMed ID: 29208524
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  • 3. Inhibitory activity evaluation and mechanistic studies of tetracyclic oxindole derivatives as α-glucosidase inhibitors.
    Sun H, Zhang Y, Ding W, Zhao X, Song X, Wang D, Li Y, Han K, Yang Y, Ma Y, Wang R, Wang D, Yu P.
    Eur J Med Chem; 2016 Nov 10; 123():365-378. PubMed ID: 27487567
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  • 4. Synthesis, Biological Evaluation, and Molecular Docking Studies of Novel Isatin-Thiazole Derivatives as α-Glucosidase Inhibitors.
    Xie Z, Wang G, Wang J, Chen M, Peng Y, Li L, Deng B, Chen S, Li W.
    Molecules; 2017 Apr 20; 22(4):. PubMed ID: 28425975
    [Abstract] [Full Text] [Related]

  • 5. Synthesis, in vitro evaluation and molecular docking studies of novel coumarin-isatin derivatives as α-glucosidase inhibitors.
    Wang G, Wang J, He D, Li X, Li J, Peng Z.
    Chem Biol Drug Des; 2017 Mar 20; 89(3):456-463. PubMed ID: 27616456
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  • 6. Synthesis, In Vitro α-Glucosidase Inhibitory Activity and Molecular Docking Studies of Novel Benzothiazole-Triazole Derivatives.
    Gong Z, Peng Y, Qiu J, Cao A, Wang G, Peng Z.
    Molecules; 2017 Sep 15; 22(9):. PubMed ID: 28914795
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  • 9. Synthesis and molecular docking studies of potent α-glucosidase inhibitors based on biscoumarin skeleton.
    Khan KM, Rahim F, Wadood A, Kosar N, Taha M, Lalani S, Khan A, Fakhri MI, Junaid M, Rehman W, Khan M, Perveen S, Sajid M, Choudhary MI.
    Eur J Med Chem; 2014 Jun 23; 81():245-52. PubMed ID: 24844449
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  • 15. Synthesis, biological evaluation and molecular docking studies of chromone hydrazone derivatives as α-glucosidase inhibitors.
    Wang G, Chen M, Wang J, Peng Y, Li L, Xie Z, Deng B, Chen S, Li W.
    Bioorg Med Chem Lett; 2017 Jul 01; 27(13):2957-2961. PubMed ID: 28506754
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  • 17. Synthesis, in vitro evaluation and molecular docking studies of thiazole derivatives as new inhibitors of α-glucosidase.
    Rahim F, Ullah H, Javid MT, Wadood A, Taha M, Ashraf M, Shaukat A, Junaid M, Hussain S, Rehman W, Mehmood R, Sajid M, Khan MN, Khan KM.
    Bioorg Chem; 2015 Oct 01; 62():15-21. PubMed ID: 26162519
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  • 18. Synthesis, biological evaluation and molecular docking study of N-arylbenzo[d]oxazol-2-amines as potential α-glucosidase inhibitors.
    Wang G, Peng Z, Wang J, Li J, Li X.
    Bioorg Med Chem; 2016 Nov 01; 24(21):5374-5379. PubMed ID: 27614916
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