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Journal Abstract Search
331 related items for PubMed ID: 37241920
1. Synthesis and Molecular Docking Studies of Alkoxy- and Imidazole-Substituted Xanthones as α-Amylase and α-Glucosidase Inhibitors. Aguila-Muñoz DG, Vázquez-Lira G, Sarmiento-Tlale E, Cruz-López MC, Jiménez-Montejo FE, López Y López VE, Escalante CH, Andrade-Pavón D, Gómez-García O, Tamariz J, Mendieta-Moctezuma A. Molecules; 2023 May 18; 28(10):. PubMed ID: 37241920 [Abstract] [Full Text] [Related]
2. Unveiling anti-diabetic potential of new thiazole-sulfonamide derivatives: Design, synthesis, in vitro bio-evaluation targeting DPP-4, α-glucosidase, and α-amylase with in-silico ADMET and docking simulation. Khamees Thabet H, Ammar YA, Imran M, Hamdy Helal M, Ibrahim Alaqel S, Alshehri A, Ash Mohd A, Abusaif MS, Ragab A. Bioorg Chem; 2024 Oct 18; 151():107671. PubMed ID: 39067419 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
4. Novel carbazole-oxadiazole derivatives as anti-α-glucosidase and anti-α-amylase agents: Design, synthesis, molecular docking, and biological evaluation. Luo S, Zhao L, Peng H, Peng Z, Wang G. Eur J Med Chem; 2024 Sep 05; 275():116600. PubMed ID: 38889608 [Abstract] [Full Text] [Related]
5. Design and synthesis of novel xanthone-triazole derivatives as potential antidiabetic agents: α-Glucosidase inhibition and glucose uptake promotion. Ye GJ, Lan T, Huang ZX, Cheng XN, Cai CY, Ding SM, Xie ML, Wang B. Eur J Med Chem; 2019 Sep 01; 177():362-373. PubMed ID: 31158750 [Abstract] [Full Text] [Related]
9. Benzimidazole Bearing Thiosemicarbazone Derivatives Act as Potent α-Amylase and α-Glucosidase Inhibitors; Synthesis, Bioactivity Screening and Molecular Docking Study. Ullah H, Khan S, Rahim F, Taha M, Iqbal R, Sarfraz M, Shah SAA, Sajid M, Awad MF, Omran A, Albalawi MA, Abdelaziz MA, Al Areefy A, Jafri I. Molecules; 2022 Oct 15; 27(20):. PubMed ID: 36296520 [Abstract] [Full Text] [Related]
11. 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 15; 106():104489. PubMed ID: 33272713 [Abstract] [Full Text] [Related]
12. Multicomponent reaction for the synthesis of new 1,3,4-thiadiazole-thiazolidine-4-one molecular hybrids as promising antidiabetic agents through α-glucosidase and α-amylase inhibition. Gummidi L, Kerru N, Ebenezer O, Awolade P, Sanni O, Islam MS, Singh P. Bioorg Chem; 2021 Oct 15; 115():105210. PubMed ID: 34332231 [Abstract] [Full Text] [Related]
13. Synthesis of indole derivatives as diabetics II inhibitors and enzymatic kinetics study of α-glucosidase and α-amylase along with their in-silico study. Taha M, Alrashedy AS, Almandil NB, Iqbal N, Anouar EH, Nawaz M, Uddin N, Chigurupati S, Wadood A, Rahim F, Das S, Venugopal V, Nawaz F, Khan KM. Int J Biol Macromol; 2021 Nov 01; 190():301-318. PubMed ID: 34481854 [Abstract] [Full Text] [Related]
14. Discovery of new anti-diabetic potential agents based on paracetamol incorporating sulfa-drugs: Design, synthesis, α-amylase, and α-glucosidase inhibitors with molecular docking simulation. Khamees Thabet H, Ragab A, Imran M, Helal MH, Ibrahim Alaqel S, Alshehri A, Ash Mohd A, Rakan Alshammari M, S Abusaif M, A Ammar Y. Eur J Med Chem; 2024 Sep 05; 275():116589. PubMed ID: 38878516 [Abstract] [Full Text] [Related]
15. Discovery of novel thiazole derivatives containing pyrazole scaffold as PPAR-γ Agonists, α-Glucosidase, α-Amylase and COX-2 inhibitors; Design, synthesis and in silico study. Fadaly WAA, Elshewy A, Nemr MTM, Abdou K, Sayed AM, Kahk NM. Bioorg Chem; 2024 Nov 05; 152():107760. PubMed ID: 39197383 [Abstract] [Full Text] [Related]