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PUBMED FOR HANDHELDS

Journal Abstract Search


730 related items for PubMed ID: 26432614

  • 1.
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  • 2. 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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  • 5. Hetarylcoumarins: Synthesis and biological evaluation as potent α-glucosidase inhibitors.
    Chaudhry F, Choudhry S, Huma R, Ashraf M, Al-Rashida M, Munir R, Sohail R, Jahan B, Munawar MA, Khan MA.
    Bioorg Chem; 2017 Aug 23; 73():1-9. PubMed ID: 28521172
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  • 6. Isatin based Schiff bases as inhibitors of α-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies.
    Rahim F, Malik F, Ullah H, Wadood A, Khan F, Javid MT, Taha M, Rehman W, Ur Rehman A, Khan KM.
    Bioorg Chem; 2015 Jun 23; 60():42-8. PubMed ID: 25955493
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  • 7. Design, synthesis and biological evaluation of novel coumarin thiazole derivatives as α-glucosidase inhibitors.
    Wang G, He D, Li X, Li J, Peng Z.
    Bioorg Chem; 2016 Apr 23; 65():167-74. PubMed ID: 26964016
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  • 8. Biscoumarin-1,2,3-triazole hybrids as novel anti-diabetic agents: Design, synthesis, in vitro α-glucosidase inhibition, kinetic, and docking studies.
    Asgari MS, Mohammadi-Khanaposhtani M, Kiani M, Ranjbar PR, Zabihi E, Pourbagher R, Rahimi R, Faramarzi MA, Biglar M, Larijani B, Mahdavi M, Hamedifar H, Hajimiri MH.
    Bioorg Chem; 2019 Nov 23; 92():103206. PubMed ID: 31445191
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  • 9. Novel pyridine-2,4,6-tricarbohydrazide thiourea compounds as small key organic molecules for the potential treatment of type-2 diabetes mellitus: In vitro studies against yeast α- and β-glucosidase and in silico molecular modeling.
    Rehman TU, Riaz S, Khan IU, Ashraf M, Bajda M, Gawalska A, Yar M.
    Arch Pharm (Weinheim); 2018 Jan 23; 351(1):. PubMed ID: 29194730
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  • 10. Syntheses of new 3-thiazolyl coumarin derivatives, in vitro α-glucosidase inhibitory activity, and molecular modeling studies.
    Salar U, Taha M, Khan KM, Ismail NH, Imran S, Perveen S, Gul S, Wadood A.
    Eur J Med Chem; 2016 Oct 21; 122():196-204. PubMed ID: 27371923
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  • 11. A new entry into the portfolio of α-glucosidase inhibitors as potent therapeutics for type 2 diabetes: Design, bioevaluation and one-pot multi-component synthesis of diamine-bridged coumarinyl oxadiazole conjugates.
    Kazmi M, Zaib S, Ibrar A, Amjad ST, Shafique Z, Mehsud S, Saeed A, Iqbal J, Khan I.
    Bioorg Chem; 2018 Apr 21; 77():190-202. PubMed ID: 29421697
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  • 15. Synthesis of Novel Triazinoindole-Based Thiourea Hybrid: A Study on α-Glucosidase Inhibitors and Their Molecular Docking.
    Taha M, Alshamrani FJ, Rahim F, Hayat S, Ullah H, Zaman K, Imran S, Khan KM, Naz F.
    Molecules; 2019 Oct 23; 24(21):. PubMed ID: 31652777
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  • 16. 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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  • 19. 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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