Results 131 to 140 of about 5,907 (191)
Inhibition mechanism and behaviour of wedelolactone against α-glucosidase. [PDF]
J Enzyme Inhib Med ChemZhang J, Zhao M, Wu F, Shi Z, Xie R.
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Gossypium hirsutum gene of unknown function Gohir.A02G131900 encodes a potential plant-specific, dual-domain exo-1,3-β-glucosidase. [PDF]
MicroPubl BiolHernandez G, Hulse-Kemp AM, Storm AR.
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A thermostable and highly active fungal GH3 β-glucosidase generated by random and saturation mutagenesis. [PDF]
Proc Jpn Acad Ser B Phys Biol SciMatsuzaki C +8 more
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Macroalgal Peptides with Predicted α-Glucosidase Inhibitory Activity: Preparation and Molecular Docking. [PDF]
Mar DrugsGhelichi S +4 more
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Jeju Citrus (Citrus unshiu) Leaf Extract and Hesperidin Inhibit Small Intestinal α-Glucosidase Activities In Vitro and Postprandial Hyperglycemia in Animal Model. [PDF]
Int J Mol SciKim GJ +8 more
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Endocrinology and Metabolism Clinics of North America, 1997
Alpha-glucosidase inhibitors are antihyperglycemic agents that lower blood glucose by delaying the digestion and absorption of complex carbohydrates. They are competitive inhibitors of the enzymes in the brush border of enterocytes that cleave eligosaccharides to monosaccharides.
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Alpha-glucosidase inhibitors are antihyperglycemic agents that lower blood glucose by delaying the digestion and absorption of complex carbohydrates. They are competitive inhibitors of the enzymes in the brush border of enterocytes that cleave eligosaccharides to monosaccharides.
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Alpha-glucosidases in human urine
Clinica Chimica Acta, 1967Abstract Two α-glucosidases from human urine have been separated by means of Sephadex G-200 gel filtration and further purified by DEAE-Sephadex chromatography. Both enzymes hydrolyse maltose and glycogen to free glucose. Indirect evidence has been obtained of the possible occurrence of further α-glucosidases in human urine.
C, Franzini, P A, Bonini
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Biochemistry. Biokhimiia, 2001
This review highlights the main properties of mammalian, plant, and microbial alpha-glucosidases. Special attention is given to the classification of these enzymes, possible catalytic mechanisms, their tertiary structure, and the structure of major inhibitors.
V V, Krasikov, D V, Karelov, L M, Firsov
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This review highlights the main properties of mammalian, plant, and microbial alpha-glucosidases. Special attention is given to the classification of these enzymes, possible catalytic mechanisms, their tertiary structure, and the structure of major inhibitors.
V V, Krasikov, D V, Karelov, L M, Firsov
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Acid alpha-glucosidase deficiency (Pompe disease)
Current Neurology and Neuroscience Reports, 2007The development and recent approval of recombinant acid alpha-glucosidase for enzyme replacement therapy have been major milestones in Pompe disease research. Acid alpha-glucosidase is the enzyme responsible for degradation of glycogen polymers to glucose in the acidic milieu of the lysosomes.
Tokiko, Fukuda +3 more
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