- Signaling Pathways
- Metabolic Enzyme/Protease
- Glycosidase
Glycosidase
Glycosidase
- [1]. Wang X, et al. Metabolites extracted from microorganisms as potential inhibitors of glycosidases (α-glucosidase and α-amylase): A review. Front Microbiol. 2022 Nov 17;13:1050869.
- [2]. Ohtsubo K, et al. Glycosylation in cellular mechanisms of health and disease. Cell. 2006 Sep 8;126(5):855-67. [Content Brief]
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Glycosidase Substrates
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Glycosidase Related Products (697)
Related Products (697)
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Antibodies (3)
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β-Galactosidase, Sweet almond
0 Imagesβ-Galactosidase, Sweet almond is a glycoside hydrolase that hydrolyzes the β-glycosidic bonds formed between galactose and its organic moieties. β-Galactosidase, Sweet almond can hydrolyze lactose to form glucose and galactose, and enter glycolysis; it can also catalyze the transgalactosylation of lactose into allolactose; allolactose can be cracked into monosaccharides. -
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Alpha-1,6-fucosidase C
0 ImagesCat. No.: HY-E70029ASynonyms: AlfCAlpha-1,6-fucosidase C (AlfC) is a GH29 fucosidase that shows specificity to α1,6-linked Fuc48. -
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HPA-IN-2
0 ImagesCat. No.: HY-143269CAS No.: 2885971-91-3HPA-IN-2 (Compound 2a-1) is a potent and selective human pancreatic α-amylase (HPA) inhibitor with IC50 values of 8.2 μM and 450.7 μM against HPA and α-glucosidase, respectively. -
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Delphinidin-3-O-galactoside chloride (Standard)
0 ImagesCat. No.: HY-N6606RCAS No.: 28500-00-7Delphinidin-3-O-galactoside chloride (Standard) is the analytical standard of Delphinidin-3-O-galactoside chloride (HY-N6606). This product is intended for research and analytical applications. Delphinidin-3-O-galactoside chloride is an anthocyanin found in abbiteye blueberry. Delphinidin-3-O-galactoside chloride show inhibitory activitiesagainst α-glucosidase with an IC50 of 68.33 μM, and tyrosinase with an IC50 of 34.14 μM. Delphinidin-3-O-galactoside chloride attenuates HO-1 and HSP70 messenger RNA down-regulation, suppresses cytotoxicity, reduces endoplasmic reticulum stress responses, scavenges free radicals, reduces intracellular triglyceride levels and lipid droplet accumulation. Delphinidin-3-O-galactoside chloride can be used for the researches of diabesity, melanoma and inflammation. -
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α-Glucosidase-IN-47
0 ImagesCat. No.: HY-157489CAS No.: 3029697-33-1α-Glucosidase-IN-47 (compound 8H) is a non-competitive α-glucosidase (α-glucosidase) inhibitor with IC50 value is 38.2 μM and Ki value is 38.2 μM. α-Glucosidase-IN-47 can be used in diabetes research.. -
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Dichotomine C
0 ImagesCat. No.: HY-N15708CAS No.: 755036-45-4Synonyms: (R)-(-)-Dichotomine CDichotomine C ((R)-(-)-Dichotomine C) is a β-carboline-type alkaloid with antiallergic effects. Dichotomine C inhibits the release of β-hexosaminidase in RBL-2H3 cells with an IC50 of 62 μM. Dichotomine C inhibits the releases of antigen-IgE-mediated TNF-α and IL-4 in RBL-2H3 cells with IC50s of 19 μM and 15 μM, respectively. Dichotomine C can be used for the study of type I allergic reactions. -
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Licheninase
0 ImagesCat. No.: HY-E70013ACAS No.: 37288-51-0Synonyms: EC 3.2.1.73Licheninase (EC 3.2.1.73) is a glycoside hydrolase that acts on the β-glucan cell walls of cereals, fungal and seaweeds. Licheninase specifically hydrolyzes the β(1→4) linkages in mixed-linkage β(1→3)/β(1→4)-glucans. Licheninase promotes cellulose degradation. -
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5-C-phenethyl-DNJ
0 ImagesCat. No.: HY-178202CAS No.: 2734265-58-65-C-phenethyl-DNJ is a selective α-glucosidase GAA inhibitor, with its Ki value for rhGAA being 0.81 μM. 5-C-phenethyl-DNJ exhibits extremely high selectivity for GANAB, GBA1, and GBA2. 5-C-phenethyl-DNJ can be used for the study of Pompe disease. -
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Kojibiose (Standard)
0 ImagesCat. No.: HY-113133RCAS No.: 2140-29-6Kojibiose (Standard) is the analytical standard of Kojibiose. This product is intended for research and analytical applications. Kojibiose, an orally active prebiotic disaccharide, can specifically inhibit the activity of α-glucosidase I. kojibiose is a proliferation factor for Bifidobacterium, lactic acid bacteria, and eubacteria. kojibiose is a low-calorie sweetener capable of increasing the absorption of iron. Kojibiose exhibits antitoxic activity. Kojibiose reduces hepatic expression of inflammatory markers in vivo[1][2]. -
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- SX29
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Parvisoflavone B
0 ImagesCat. No.: HY-N17601CAS No.: 50277-02-6Parvisoflavone B is a prenylated flavonoid. Parvisoflavone B can be isolated from root bark of Erythrina mildbraedii. Parvisoflavone B inhibits PTP1B activity with an IC50 of 42.6 μM. Parvisoflavone B inhibits α-glucosidase with an IC50 of 12.19 μM. Parvisoflavone B can be used in the research of type 2 diabetes and obesity. -
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α-Glucosidase-IN-91
0 ImagesCat. No.: HY-174310α-Glucosidase-IN-91 (Compound 15j) is a competitive and potent inhibitor for α-Glucosidase (IC50 = 6.6 μM). α-Glucosidase-IN-91 has a potent binding affinity towards α-Glucosidase. α-Glucosidase-IN-91 exhibits high stability, interacting and inhibiting α-Glucosidase selectively. α-Glucosidase-IN-91 can be studied in research for type 2 diabetes and blood glucose control. -
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Chalcomoracin
0 ImagesCat. No.: HY-N20674CAS No.: 76472-89-4Chalcomoracin is an orally active anticancer agent. Chalcomoracin exhibits anticancer, antibacterial, and α-glucosidase inhibitory activities, with an IC50 of 14.23 µM against yeast α-glucosidase and an IC50 of 5.5 μM against FabI of Staphylococcus aureus. Chalcomoracin reduces the phosphorylation levels of ERK, JNK, and P38; enhances the phosphorylation level of ERK1/2; regulates the MAPK, mTOR, AKT, and p53 signaling pathways; upregulates the expression of Chop, Bip, PINK1, GRP78, and GADD153; and downregulates the expression of Alix. Chalcomoracin induces apoptosis (apoptosis), endoplasmic reticulum stress (endoplasmic reticulum stress), paraptosis (paraptosis), ROS production, mitophagy (mitophagy), and autophagy (autophagy); it inhibits cancer cell viability, colony-forming ability, migration, invasion, proliferation, tumorigenesis, fatty acid synthesis, S. aureus growth, vitreous-stimulated retinal cell activity, and cell cycle progression at the G0/G1 phase. Chalcomoracin can be used in research related to hepatocellular carcinoma, non-small cell lung cancer, triple-negative breast cancer, prostate cancer, proliferative vitreoretinopathy, pancreatic cancer, diabetes, and bacterial infections. -
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α-Galactosidase, Clostridium cellulolyticum
0 ImagesCat. No.: HY-P2871Dα-Galactosidase, Clostridium cellulolyticum (EC 3.2.1.22) is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. Two recombinant forms of α-Galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). -
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α-Glucosidase-IN-125
0 ImagesCat. No.: HY-189401α-Glucosidase-IN-125 (compound 7h) is a potent α-glucosidase (α-glucosidase) inhibitor with an IC50 of 20.73 μM. α-Glucosidase-IN-125 inhibits α-glucosidase activity by binding to the active site of α-glucosidase, thereby delaying carbohydrate digestion and reducing postprandial hyperglycemia. α-Glucosidase-IN-125 can be used for research on type 2 diabetes. -
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β-Mannosidase, Bacteroides thetaiotaomicron
0 ImagesCat. No.: HY-P2858Bβ-Mannosidase, Bacteroides thetaiotaomicron (EC 3.2.1.25), is the final exoglycosidase in the N-linked glycoprotein oligosaccharide catabolism pathway. β-Mannosidase catalyzes the following chemical reaction: hydrolysis of the terminal non-reducing β-D-mannose residue in β-D-mannoside. -
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2'-Rhamnoechinacoside
0 ImagesCat. No.: HY-N13188CAS No.: 1422390-59-7Synonyms: Michelioside A2'-Rhamnoechinacoside (Michelioside A), a compound of phenylethanoid glycosides, is a α-glucosidase inhibitor with anti-tumor activity, which is derived from Phlomis stewartii. 2'-Rhamnoechinacoside can be used for research of UV-absorbing and cancers. -
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- α-Glucosidase-IN-31
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α-Glucosidase-IN-124
0 ImagesCat. No.: HY-189389α-Glucosidase-IN-124 is an α-glucosidase inhibitor with an IC50 of 18.55 μM. α-Glucosidase-IN-124 also exhibits inhibitory activity against α-amylase. α-Glucosidase-IN-124 delays carbohydrate digestion and reduces postprandial hyperglycemia by inhibiting α-glucosidase and α-amylase. α-Glucosidase-IN-124 can be used in diabetes-related research. -
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α-Glucosidase-IN-109
0 ImagesCat. No.: HY-181091α-Glucosidase-IN-109 is an orally active α-glucosidase inhibitor with an IC50 of 0.0136 μM. α-Glucosidase-IN-109 modulates carbohydrate and lipid metabolism, reduces fasting blood glucose levels, alleviates weight loss, and exhibits protective effects on liver and kidney function. α-Glucosidase-IN-109 can be used in research related to type 2 diabetes. -
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