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Journal Abstract Search

485 related items for PubMed ID: 31158750

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  • 23. Inhibition of the carbohydrate-hydrolyzing enzymes α-amylase and α-glucosidase by hydroxylated xanthones.
    Santos CMM, Proença C, Freitas M, Araújo AN, Silva AMS, Fernandes E.
    Food Funct; 2022 Jul 18; 13(14):7930-7941. PubMed ID: 35788613
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  • 25. Synthesis, α-glucosidase inhibition, and molecular docking studies of novel N-substituted hydrazide derivatives of atranorin as antidiabetic agents.
    Duong TH, Paramita Devi A, Tran NM, Phan HV, Huynh NV, Sichaem J, Tran HD, Alam M, Nguyen TP, Nguyen HH, Chavasiri W, Nguyen TC.
    Bioorg Med Chem Lett; 2020 Sep 01; 30(17):127359. PubMed ID: 32738998
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  • 27. Synthesis of 1H-1,2,3-triazole derivatives as new α-glucosidase inhibitors and their molecular docking studies.
    Avula SK, Khan A, Rehman NU, Anwar MU, Al-Abri Z, Wadood A, Riaz M, Csuk R, Al-Harrasi A.
    Bioorg Chem; 2018 Dec 01; 81():98-106. PubMed ID: 30118991
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  • 28. Discovery of new 2-phenyl-1H-benzo[d]imidazole core-based potent α-glucosidase inhibitors: Synthesis, kinetic study, molecular docking, and in vivo anti-hyperglycemic evaluation.
    Li Y, Zhang JH, Xie HX, Ge YX, Wang KM, Song ZL, Zhu KK, Zhang J, Jiang CS.
    Bioorg Chem; 2021 Dec 01; 117():105423. PubMed ID: 34717239
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  • 33. 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. In vitro and in silico studies of bis (indol-3-yl) methane derivatives as potential α-glucosidase and α-amylase inhibitors.
    Zheng PF, Xiong Z, Liao CY, Zhang X, Feng M, Wu XZ, Lin J, Lei LS, Zhang YC, Wang SH, Xu XT.
    J Enzyme Inhib Med Chem; 2021 Dec 01; 36(1):1938-1951. PubMed ID: 34459690
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  • 36. 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 01; 77():190-202. PubMed ID: 29421697
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  • 38. Binding mechanism and synergetic effects of xanthone derivatives as noncompetitive α-glucosidase inhibitors: a theoretical and experimental study.
    Liu Y, Ma L, Chen WH, Park H, Ke Z, Wang B.
    J Phys Chem B; 2013 Oct 31; 117(43):13464-71. PubMed ID: 24083955
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  • 39. Pyridine sulfonamide as a small key organic molecule for the potential treatment of type-II diabetes mellitus and Alzheimer's disease: In vitro studies against yeast α-glucosidase, acetylcholinesterase and butyrylcholinesterase.
    Riaz S, Khan IU, Bajda M, Ashraf M, Qurat-Ul-Ain, Shaukat A, Rehman TU, Mutahir S, Hussain S, Mustafa G, Yar M.
    Bioorg Chem; 2015 Dec 31; 63():64-71. PubMed ID: 26451651
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  • 40. New carbazole linked 1,2,3-triazoles as highly potent non-sugar α-glucosidase inhibitors.
    Iqbal S, Khan MA, Javaid K, Sadiq R, Fazal-Ur-Rehman S, Choudhary MI, Basha FZ.
    Bioorg Chem; 2017 Oct 31; 74():72-81. PubMed ID: 28756277
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