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Synthesis and biological evaluation of novel 2,4,5-triarylimidazole-1,2,3-triazole derivatives via click chemistry asa-glucosidase inhibitors.

Jishou University

Ionic liquid-promoted multicomponent synthesis of fused tetrazolo[1,5-a]pyrimidines asa-glucosidase inhibitors.

National Institute of Technology Karnataka

Inhibitory Effects of Highly Oxygenated Lanostane Derivatives from the Fungus Ganoderma lucidum on P-Glycoprotein anda-Glucosidase.

Chinese Academy of Sciences

Synthesis of diethyl 4-substituted-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylates as a new series of inhibitors against yeasta-glucosidase.

University of Karachi

Design, synthesis and docking study of novel tetracyclic oxindole derivatives asa-glucosidase inhibitors.

Key Laboratory of Industrial Fermentation Microbiology (Tianjin University of Science and Technology)

Synthesis of novel indenoquinoxaline derivatives as potenta-glucosidase inhibitors.

University of The Punjab

Synthesis anda-glucosidase inhibitory activity evaluation of N-substituted aminomethyl-ß-d-glucopyranosides.

Xi'An Jiaotong University

(3R,4S,5R,6R,7S)-3,4,5,7-Tetrahydroxyconidine, an azetidine analogue of 6,7-diepicastanospermine and a conformationally constrained d-deoxyaltronojirimycin, from l-arabinose.

University of Oxford

Mexican antidiabetic herbs: valuable sources of inhibitors ofa-glucosidases.

Universidad Nacional Aut£Noma De M£Xico

Synthesis, biological activity, and molecular modeling studies of 1H-1,2,3-triazole derivatives of carbohydrates as alpha-glucosidases inhibitors.

Universidade Federal Do Rio De Janeiro

Biological properties of D- and L-1-deoxyazasugars.

Toyama Medical and Pharmaceutical University

Alpha-1-C-alkyl-1-deoxynojirimycin derivatives as potent and selective inhibitors of intestinal isomaltase: remarkable effect of the alkyl chain length on glycosidase inhibitory profile.

Universit£

Nitrogen-in-the-ring pyranoses and furanoses: structural basis of inhibition of mammalian glycosidases.

Hokuriku University

 

Potent glycosidase inhibitors, N-phenyl cyclic isourea derivatives of 5-amino- and 5-amino-1-C-(hydroxymethyl)-cyclopentane-1,2,3,4-tetraols

TBA

Towards a stable noeuromycin analog with a D-manno configuration: synthesis and glycosidase inhibition of D-manno-like tri- and tetrahydroxylated azepanes.

Umr Cnrs 7201

New glucocerebrosidase inhibitors by exploration of chemical diversity of N-substituted aminocyclitols using click chemistry and in situ screening.

Spanish National Research Council (Consejo Superior De Investigaciones Cienti£?Ficas)

Selectivea-glucosidase substrates and inhibitors containing short aromatic peptidyl moieties.

Seoul National University

Fluorescent-tagged sp2-iminosugars with potentß-glucosidase inhibitory activity.

Universidad De Sevilla

Amplification of the inhibitory activity of miglitol by monofluorination.

Martin-Luther-Universit£T Halle-Wittenberg

New polyhydroxylated pyrrolidine, piperidine, and pyrrolizidine alkaloids from Scilla sibirica.

Hokuriku University

Hybrid angiogenesis inhibitors: synthesis and biological evaluation of bifunctional compounds based on 1-deoxynojirimycin and aryl-1,2,3-triazoles.

University College Dublin

Synthesis of valiolamine and some precursors for bioactive carbaglycosylamines from (-)-vibo-quercitol produced by biogenesis of myo-inositol.

Keio University

Aglycon specificity profiling of alpha-glucosidases using synthetic probes.

Institute of Physical and Chemical Research (Riken)

Polyhydroxylated azetidine iminosugars: Synthesis, glycosidase inhibitory activity and molecular docking studies.

Savitribai Phule Pune University

Pyrimidine-fused heterocycle derivatives as a novel class of inhibitors for a-glucosidase.

Shiraz University

Structure-activity relationships of bergenin derivatives effect on a-glucosidase inhibition.

Kinki University

Green synthesis, inhibition studies of yeast a-glucosidase and molecular docking of pyrazolylpyridazine amines.

University of The Punjab

In search of new a-glucosidase inhibitors: Imidazolylpyrazole derivatives.

University of The Punjab

Synthesis, molecular docking studies of hybrid benzimidazole as a-glucosidase inhibitor.

Universiti Teknologi Mara (Uitm)

Design, synthesis and biological evaluation of novel coumarin thiazole derivatives as a-glucosidase inhibitors.

Jishou University

Synthesis, a-glucosidase inhibitory, cytotoxicity and docking studies of 2-aryl-7-methylbenzimidazoles.

Universiti Teknologi Mara (Uitm), Puncak Alam Campus

Dihydropyrano [2,3-c] pyrazole: Novel in vitro inhibitors of yeast a-glucosidase.

King Abdulaziz University

Synthesis, In vitro and Docking Studies of New Flavone Ethers as a-Glucosidase Inhibitors.

Universiti Teknologi Mara

Benzimidazole derivatives as new a-glucosidase inhibitors and in silico studies.

Universiti Teknologi Mara (Uitm)

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 a-glucosidase, acetylcholinesterase and butyrylcholinesterase.

Gc University

Synthesis, in vitro evaluation and molecular docking studies of biscoumarin thiourea as a new inhibitor of a-glucosidases.

Universiti Teknologi Mara

Evaluation of 2-indolcarbohydrazones as potent a-glucosidase inhibitors, in silico studies and DFT based stereochemical predictions.

Universiti Teknologi Mara (Uitm)

Synthesis, in vitro evaluation and molecular docking studies of thiazole derivatives as new inhibitors of a-glucosidase.

Hazara University

Isatin based Schiff bases as inhibitors of a-glucosidase: Synthesis, characterization, in vitro evaluation and molecular docking studies.

Hazara University

Triazinoindole analogs as potent inhibitors of a-glucosidase: synthesis, biological evaluation and molecular docking studies.

Hazara University

Organocatalyzed solvent free an efficient novel synthesis of 2,4,5-trisubstituted imidazoles for a-glucosidase inhibition to treat diabetes.

Comsats Institute of Information Technology

Novel synthesis of dihydropyrimidines for a-glucosidase inhibition to treat type 2 diabetes: in vitro biological evaluation and in silico docking.

Comsats Institute of Information Technology

New insights into the pharmacological chaperone activity of c2-substituted glucoimidazoles for the treatment of Gaucher disease.

Nankai University

Antioxidant, a-glucosidase and xanthine oxidase inhibitory activity of bioactive compounds from maize (Zea mays L.).

Srtm University

A novel competitive class of α-glucosidase inhibitors: (E)-1-phenyl-3-(4-styrylphenyl)urea derivatives.

Gyeongsang National University