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PUBMED FOR HANDHELDS

Journal Abstract Search


274 related items for PubMed ID: 34666184

  • 1. Peptide conjugates of 18β-glycyrrhetinic acid as potent inhibitors of α-glucosidase and AGEs-induced oxidation.
    Khan SN, Shaheen F, Aleem U, Sheikh S, Tamfu AN, Ashraf S, Ul-Haq Z, Ullah S, Wahab AT, Choudhary MI, Jahan H.
    Eur J Pharm Sci; 2022 Jan 01; 168():106045. PubMed ID: 34666184
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 3. Novel Coumarin Containing Dithiocarbamate Derivatives as Potent α-Glucosidase Inhibitors for Management of Type 2 Diabetes.
    Mollazadeh M, Mohammadi-Khanaposhtani M, Valizadeh Y, Zonouzi A, Faramarzi MA, Kiani M, Biglar M, Larijani B, Hamedifar H, Mahdavi M, Hajimiri MH.
    Med Chem; 2021 Apr 01; 17(3):264-272. PubMed ID: 32851964
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  • 4. Design, synthesis, docking study, α-glucosidase inhibition, and cytotoxic activities of acridine linked to thioacetamides as novel agents in treatment of type 2 diabetes.
    Mohammadi-Khanaposhtani M, Rezaei S, Khalifeh R, Imanparast S, Faramarzi MA, Bahadorikhalili S, Safavi M, Bandarian F, Nasli Esfahani E, Mahdavi M, Larijani B.
    Bioorg Chem; 2018 Oct 01; 80():288-295. PubMed ID: 29980114
    [Abstract] [Full Text] [Related]

  • 5. Design and synthesis of novel pyrazole-phenyl semicarbazone derivatives as potential α-glucosidase inhibitor: Kinetics and molecular dynamics simulation study.
    Azimi F, Ghasemi JB, Azizian H, Najafi M, Faramarzi MA, Saghaei L, Sadeghi-Aliabadi H, Larijani B, Hassanzadeh F, Mahdavi M.
    Int J Biol Macromol; 2021 Jan 01; 166():1082-1095. PubMed ID: 33157144
    [Abstract] [Full Text] [Related]

  • 6. Comparative study of selective in vitro and in silico BACE1 inhibitory potential of glycyrrhizin together with its metabolites, 18α- and 18β-glycyrrhetinic acid, isolated from Hizikia fusiformis.
    Wagle A, Seong SH, Zhao BT, Woo MH, Jung HA, Choi JS.
    Arch Pharm Res; 2018 Apr 01; 41(4):409-418. PubMed ID: 29532412
    [Abstract] [Full Text] [Related]

  • 7. Design and synthesis of novel quinazolinone-1,2,3-triazole hybrids as new anti-diabetic agents: In vitro α-glucosidase inhibition, kinetic, and docking study.
    Saeedi M, Mohammadi-Khanaposhtani M, Pourrabia P, Razzaghi N, Ghadimi R, Imanparast S, Faramarzi MA, Bandarian F, Esfahani EN, Safavi M, Rastegar H, Larijani B, Mahdavi M, Akbarzadeh T.
    Bioorg Chem; 2019 Mar 01; 83():161-169. PubMed ID: 30366316
    [Abstract] [Full Text] [Related]

  • 8. Synthesis and biological evaluation of new benzimidazole-1,2,3-triazole hybrids as potential α-glucosidase inhibitors.
    Asemanipoor N, Mohammadi-Khanaposhtani M, Moradi S, Vahidi M, Asadi M, Faramarzi MA, Mahdavi M, Biglar M, Larijani B, Hamedifar H, Hajimiri MH.
    Bioorg Chem; 2020 Jan 01; 95():103482. PubMed ID: 31838286
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  • 14. 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 01; 78():269-279. PubMed ID: 29614438
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  • 16. Anti-psoriasis effect of 18β-glycyrrhetinic acid by breaking CCL20/CCR6 axis through its vital active group targeting GUSB/ATF2 signaling.
    Wei J, Zhang J, Hu F, Zhang W, Wu Y, Liu B, Lu Y, Li L, Han L, Lu C.
    Phytomedicine; 2024 Jun 01; 128():155524. PubMed ID: 38552435
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  • 18. Ultrasonic synthesis of tyramine derivatives as novel inhibitors of α-glucosidase in vitro.
    Siddiqui H, Bashir MA, Javaid K, Nizamani A, Bano H, Yousuf S, Rahman AU, Choudhary MI.
    J Enzyme Inhib Med Chem; 2016 Dec 01; 31(6):1392-403. PubMed ID: 26912275
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  • 20. Synthesis of azachalcones, their α-amylase, α-glucosidase inhibitory activities, kinetics, and molecular docking studies.
    Saleem F, Kanwal, Khan KM, Chigurupati S, Solangi M, Nemala AR, Mushtaq M, Ul-Haq Z, Taha M, Perveen S.
    Bioorg Chem; 2021 Jan 01; 106():104489. PubMed ID: 33272713
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