- 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 Inhibitors
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Glycosidase Substrates
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Glycosidase Ligands
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Glycosidase Related Products (688)
Related Products (688)
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Antibodies (3)
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EB-0176
0 ImagesCat. No.: HY-145275CAS No.: 2758314-64-4EB-0176 is a potent inhibitor of ER α-glucosidases (α-Glu) Iand II with IC50s of 0.6439 and 0.0011 μM, respectively. EB-0176 is a N-substituted derivative of valiolamine with broad-spectrum antiviral. EB-0176 has the potential for the reseach of broad-spectrum agent against the existing and emerging viruses. -
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β-Glucosidase 1A, Thermus thermophilus
0 ImagesCat. No.: HY-E71305Kβ-Glucosidase 1A, Thermus thermophilus (EC 3.2.1.21) is a glucosidase enzyme that acts upon β1->4 bonds linking two glucose or glucose-substituted molecules (i.e., the disaccharide cellobiose) . β-Glucosidase is one of the cellulases, enzymes involved in the decomposition of cellulose and related polysaccharides; more specifically, an exocellulase with specificity for a variety of beta-D-glycoside substrates. It catalyzes the hydrolysis of terminal non-reducing residues in beta-D-glucosides with release of glucose. -
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PBI-6DNJ
0 ImagesCat. No.: HY-150723CAS No.: 2857098-72-5PBI-6DNJ is an orally active and potent multivalent glycosidase inhibitor. PBI-6DNJ exhibits good inhibition activity against α-glucosidase from mice, with a Ki of 0.14 μM. PBI-6DNJ exhibits good hypoglycemic activity. PBI-6DNJ can be used for type 2 diabetes research. -
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α-Glucosidase-IN-57
0 ImagesCat. No.: HY-163433CAS No.: 3034302-49-0α-Glucosidase-IN-57 (Compound 10c) is a competitive and orally active α-glucosidase inhibitor with an IC50 value of 0.180 μM and a Ki of 0.15 μM. α-Glucosidase-IN-57 can reduce fasting and overall blood glucose levels in mice, and can be used for anti-diabetes research. -
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Theophylline-triazole-estrone
0 ImagesCat. No.: HY-187715Theophylline-triazole-estrone is an α-glucosidase inhibitor with an IC50 of 123.9 μM. Theophylline-triazole-estrone interacts with the catalytic site of α-glucosidase and binds to the anti-apoptotic protein BCL-2. Theophylline-triazole-estrone reduces cancer cell viability and can be used in research related to type 2 diabetes and breast cancer. -
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α1-3,4 Fucosidase, Sweet almond
0 ImagesCat. No.: HY-132177Jα1-3,4 Fucosidase, Sweet almond is an enzyme that breaks down fucose. Fucosidosis is an autosomal recessive lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues. -
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ABCB1-IN-4
0 ImagesCat. No.: HY-168944CAS No.: 1500779-21-4ABCB1-IN-4 (Compound C6z) is an orally active and potent dual α-amylase and α-glucosidase inhibitor with IC50 values of 1.63 μM and 0.14 μM, respectively. ABCB1-IN-4 is promising for research of diabetes. -
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G721-0282
0 ImagesG721-0282 is an orally active CHI3L1 inhibitor. G721-0282 can reduce the expression of inflammatory proteins and cytokines. G721-0282 inhibits the activation of the NF-κB signaling pathway. G721-0282 inhibits neuroinflammation and reduces anxious behavior. G721-0282 significantly inhibits the proliferation of osteosarcoma (OS) cells by suppressing the STAT3 signaling pathway. G721-0282 induces OS cell apoptosis by upregulating pro-apoptotic protein levels and downregulating anti-apoptotic protein levels. G721-0282 can be used for researches on neuroinflammatory conditions and cancer. -
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Panaxjapyne A
0 ImagesCat. No.: HY-N22020CAS No.: 1242413-82-6Panaxjapyne A is a baker's yeast α-glucosidase inhibitor with an IC50 of 71.82 μM. Panaxjapyne A can be used in diabetes-related research. -
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Antibacterial agent 207
0 ImagesCat. No.: HY-162451Antibacterial agent 207 (Compound Ru1) has antibacterial activity against S. aureus (MIC: 1 μg/mL), and low resistance frequencies. Antibacterial agent 207 destroys the bacterial cell membrane, promote production of ROS in bacteria. -
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- α2-3 Neuraminidase, Salmonella typhimurium LT2
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16-Oxoserratenediol
0 ImagesCat. No.: HY-N16575CAS No.: 24513-52-816-Oxoserratenediol (Compound 11) is a serratene-type triterpenoid found in Lycopodium cernuum L.. 16-Oxoserratenediol is a α-glucosidase inhibitor with inhibition rate of 43.93% at 100 μM. 16-Oxoserratenediol can be used for the research of diabetes. -
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Deacylhericene
0 ImagesCat. No.: HY-N18381CAS No.: 158314-36-4Deacylhericene is an α-glucosidase inhibitor with an IC50 of 12.5 μM. Deacylhericene functionally inhibits the activity of α-glucosidase. -
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- α-Glucosidase-IN-40
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Quinoline-2-carboxylic acid-d6
0 ImagesCat. No.: HY-W002011SCAS No.: 1219802-18-2Quinoline-2-carboxylic acid-d6 is the deuterium labeled Quinoline-2-carboxylic acid (HY-W002011). Quinoline-2-carboxylic acid exhibits antidiabetic activity. Quinoline-2-carboxylic acid can be used as drug intermediate for synthesis of various active compounds. -
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α-Amylase/α-Glucosidase-IN-18
0 ImagesCat. No.: HY-168961α-Amylase/α-Glucosidase-IN-18 (Compound 9g) is the inhibitor for α-Amylase and α-Glucosidase with IC50 of 49.17 nM and 10.71 nM. α-Amylase/α-Glucosidase-IN-18 can be used in research of type 2 diabetes mellitus. -
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Antidiabetic agent 2
0 ImagesCat. No.: HY-155961CAS No.: 3052242-32-4Antidiabetic agent 2 (Compound 56) is a glucose-uptake promoter. Antidiabetic agent 2 inhibits DPP-4, PTP-1B, α-amylase, and α-glucosidase with IC50s of 0.036, 0.042, 0.241, 0.185 μM. Antidiabetic agent 2 decreases blood glucose levels. -
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(3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol
0 ImagesCat. No.: HY-W385597CAS No.: 267421-93-2(3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol (Compound 1) is a glycosidase inhibitor. (3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol is an intermediate for many active molecules. -
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Guavinoside B
0 ImagesCat. No.: HY-N17855CAS No.: 372955-18-5Guavinoside B is an orally active α-glucosidase inhibitor with an IC50 of 0.21 mM. Guavinoside B upregulates the expressions of Nrf2, GCLC and NQO1 induced by Acetaminophen (HY-66005), downregulates the expression of p-JNK, and reduces intracellular ROS levels. Guavinoside B decreases serum TNF-α levels induced by Acetaminophen, alleviates hepatocellular infiltration and necrosis, and improves liver-related biochemical parameters. Guavinoside B is applicable to the research of diabetes and Acetaminophen-induced liver injury. -
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2,3-Indolobetulonic acid
0 ImagesCat. No.: HY-134960CAS No.: 905837-93-62,3-Indolobetulonic acid (compound 2), a triterpenoid, is α-glucosidase inhibitor with an IC50 of 1.8 µM. -
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