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Journal Abstract Search

350 related items for PubMed ID: 31679980

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. Triazoloquinazolines as a new class of potent α-glucosidase inhibitors: in vitro evaluation and docking study.
    Abuelizz HA, Anouar EH, Ahmad R, Azman NIIN, Marzouk M, Al-Salahi R.
    PLoS One; 2019 Nov 10; 14(8):e0220379. PubMed ID: 31412050
    [Abstract] [Full Text] [Related]

  • 23. 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 10; 73():1-9. PubMed ID: 28521172
    [Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. Design and synthesis of 4,5-diphenyl-imidazol-1,2,3-triazole hybrids as new anti-diabetic agents: in vitro α-glucosidase inhibition, kinetic and docking studies.
    Asgari MS, Mohammadi-Khanaposhtani M, Sharafi Z, Faramarzi MA, Rastegar H, Nasli Esfahani E, Bandarian F, Ranjbar Rashidi P, Rahimi R, Biglar M, Mahdavi M, Larijani B.
    Mol Divers; 2021 May 01; 25(2):877-888. PubMed ID: 32189236
    [Abstract] [Full Text] [Related]

  • 26. Synthesis, in vitro evaluation and molecular docking studies of novel amide linked triazolyl glycoconjugates as new inhibitors of α-glucosidase.
    Gupta SJ, Dutta S, Gajbhiye RL, Jaisankar P, Sen AK.
    Bioorg Chem; 2017 Jun 01; 72():11-20. PubMed ID: 28346871
    [Abstract] [Full Text] [Related]

  • 27. Inhibition of α-glucosidase enzyme by 'click'-inspired pharmacophore framework 1,3,4-thiadiazole-1,2,3-triazole hybrids.
    Dhameja M, Kumar H, Kurella S, Singh R, Uma A, Gupta P.
    Future Med Chem; 2023 Feb 01; 15(4):345-363. PubMed ID: 36942781
    [Abstract] [Full Text] [Related]

  • 28. 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
    [Abstract] [Full Text] [Related]

  • 29. Cyanoacetohydrazide linked to 1,2,3-triazole derivatives: a new class of α-glucosidase inhibitors.
    Iraji A, Shareghi-Brojeni D, Mojtabavi S, Faramarzi MA, Akbarzadeh T, Saeedi M.
    Sci Rep; 2022 May 23; 12(1):8647. PubMed ID: 35606520
    [Abstract] [Full Text] [Related]

  • 30. Design and synthesis of new fused carbazole-imidazole derivatives as anti-diabetic agents: In vitro α-glucosidase inhibition, kinetic, and in silico studies.
    Adib M, Peytam F, Shourgeshty R, Mohammadi-Khanaposhtani M, Jahani M, Imanparast S, Faramarzi MA, Larijani B, Moghadamnia AA, Esfahani EN, Bandarian F, Mahdavi M.
    Bioorg Med Chem Lett; 2019 Mar 01; 29(5):713-718. PubMed ID: 30661823
    [Abstract] [Full Text] [Related]

  • 31. Novel N'-substituted benzylidene benzohydrazides linked to 1,2,3-triazoles: potent α-glucosidase inhibitors.
    Saeedi M, Hariri R, Iraji A, Ahmadi A, Mojtabavi S, Golshani S, Faramarzi MA, Akbarzadeh T.
    Sci Rep; 2023 Jun 02; 13(1):8960. PubMed ID: 37268722
    [Abstract] [Full Text] [Related]

  • 32. Synthesis, and In Vitro and In Silico α-Glucosidase Inhibitory Studies of 5-Chloro-2-Aryl Benzo[d]thiazoles.
    Shah S, Arshia, Javaid K, Zafar H, Mohammed Khan K, Khalil R, Ul-Haq Z, Perveen S, Iqbal Choudhary M.
    Bioorg Chem; 2018 Aug 02; 78():269-279. PubMed ID: 29614438
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  • 33. Synthesis of 4-alkylaminoimidazo[1,2-a]pyridines linked to carbamate moiety as potent α-glucosidase inhibitors.
    Saeedi M, Raeisi-Nafchi M, Sobhani S, Mirfazli SS, Zardkanlou M, Mojtabavi S, Faramarzi MA, Akbarzadeh T.
    Mol Divers; 2021 Nov 02; 25(4):2399-2409. PubMed ID: 33047276
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  • 34. Synthesis of 6-hydroxyaurone analogues and evaluation of their α-glucosidase inhibitory and glucose consumption-promoting activity: Development of highly active 5,6-disubstituted derivatives.
    Sun H, Ding W, Song X, Wang D, Chen M, Wang K, Zhang Y, Yuan P, Ma Y, Wang R, Dodd RH, Zhang Y, Lu K, Yu P.
    Bioorg Med Chem Lett; 2017 Aug 01; 27(15):3226-3230. PubMed ID: 28651984
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  • 35. Synthesis, in vitro evaluation and molecular docking studies of biscoumarin thiourea as a new inhibitor of α-glucosidases.
    Zawawi NK, Taha M, Ahmat N, Ismail NH, Wadood A, Rahim F, Rehman AU.
    Bioorg Chem; 2015 Dec 01; 63():36-44. PubMed ID: 26432614
    [Abstract] [Full Text] [Related]

  • 36. Synthesis and α-glucosidase inhibition activity of dihydroxy pyrrolidines.
    Kasturi S, Surarapu S, Uppalanchi S, Anireddy JS, Dwivedi S, Anantaraju HS, Perumal Y, Sigalapalli DK, Babu BN, Ethiraj KS.
    Bioorg Med Chem Lett; 2017 Jun 15; 27(12):2818-2823. PubMed ID: 28495082
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  • 37. 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
    [Abstract] [Full Text] [Related]

  • 38. Synthesis of indole-based-thiadiazole derivatives as a potent inhibitor of α-glucosidase enzyme along with in silico study.
    Alomari M, Taha M, Rahim F, Selvaraj M, Iqbal N, Chigurupati S, Hussain S, Uddin N, Almandil NB, Nawaz M, Khalid Farooq R, Khan KM.
    Bioorg Chem; 2021 Mar 01; 108():104638. PubMed ID: 33508679
    [Abstract] [Full Text] [Related]

  • 39. Synthesis, biological evaluation, and docking studies of novel 5,6-diaryl-1,2,4-triazine thiazole derivatives as a new class of α-glucosidase inhibitors.
    Wang G, Peng Z, Gong Z, Li Y.
    Bioorg Chem; 2018 Aug 01; 78():195-200. PubMed ID: 29587132
    [Abstract] [Full Text] [Related]

  • 40. 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
    [Abstract] [Full Text] [Related]

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