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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]