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| Product | Description | |
|---|---|---|
| α-Glucosidase | α-Glucosidase. Synonyms: alpha-Glucosidase (from Yeast) 100kU pack;a-Glucosidase (EC 3.2.1.20);β-D-Glucoside glycohydrolase (EC 3.2.1.21);MALTASE;MALTASE TYPE I;MALTASE TYPE V;A-glucosidase from bacillus*stearothermophilus ly;A-glucosidase type I from bakers yeast. CAS No. 9001-42-7. Pack Sizes: 1 kg. Product ID: CDF4-0060. Molecular formula: NULL. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; α-Glucosidase; CDF4-0060; 9001-42-7; NULL; 232-604-7; 9001-42-7. Purity: 0.99. Color: off-White. EC Number: 232-604-7. Physical State: Powder. Storage: 2-8°C. Application: For the determination of α-amylase and the synthesis of various 1'-O-sucrose and 1-O-fructose esters. Melting Point: 154.3-155.3 °C. Product Description: This product has been enhanced for energy efficiency and waste prevention when used in starch hydrolysis research. |  |
| α-Glucosidase from Escherichia coli, Recombinant | Glycoside hydrolases (also called glycosidases or glycosyl hydrolases) assist in the hydrolysis of glycosidic bonds in complex sugars. They are extremely common enzymes with roles in nature including degradation of biomass such as cellulose and hemicellulose, in anti-bacterial defense strategies (e.g., lysozyme), in pathogenesis mechanisms (e.g., viral neuraminidases) and in normal cellular function (e.g., trimming mannosidases involved in N-linked glycoprotein biosynthesis). Together with glycosyltransferases, glycosidases form the major catalytic machinery for the synthesis and breakage of glycosidic bonds. Group: Enzymes. Synonyms: Alpha-glucosidase; EC 3.2.1.20; maltase; glucoinvertase; glucosidosucra. Enzyme Commission Number: EC 3.2.1.20. CAS No. 9001-42-7. Purity: > 95 % as judged by SDS-PAGE. α-Glucosidase. Mole weight: 72992.3 Da. Activity: 34.1 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Escherichia coli str. K-12 substr. W3110. Alpha-glucosidase; EC 3.2.1.20; maltase; glucoinvertase; glucosidosucrase; maltase-glucoamylase; alpha-glucopyranosidase; glucosidoinvertase; alpha-D-glucosidase; alpha-glucoside hydrolase; alpha-1,4-glucosidase; alpha-D-glucoside glucohydrolase; glycosidases; glycosyl hydrolases; α-Glucosidase. Cat No: NATE-1177. |  |
| Native α-Glucosidase from Bacillus stearothermophilus | Alpha-glucosidase is a glucosidase located in the brush border of the small intestine that acts upon 1,4-alpha bonds. This is in contrast to beta-glucosidase. Alpha-glucosidase breaks down starch and disaccharides to glucose. Maltase, a similar enzyme that cleaves maltose, is nearly functionally equivalent. Α-glucosidase hydrolyzes carbohydrates by acting on 1,4-α linkages. inhibition of α-glucosidase is a prominent target in the management of non-insulin-dependent diabetes mellitus. Applications: Α-glucosidase is potential enzyme for the biosynthesis of complex carbohydrates. Group: Enzymes. Synonyms: Alpha-glucosidase; EC 3.2.1.20; maltase; glucoinvertase; glucosidosucrase; maltase-glucoamylase; alpha-glucopyranosidase; glucosidoinvertase; alpha-D-glucosidase; alpha-glucoside hydrolase; alpha-1,4-glucosidase; al. Enzyme Commission Number: EC 3.2.1.20. CAS No. 9001-42-7. α-Glucosidase. Activity: >50 units/mg. Storage: 2-8°C. Form: Lyophilized powder containing potassium phosphate buffer salt. Source: Bacillus stearothermophilus. Alpha-glucosidase; EC 3.2.1.20; maltase; glucoinvertase; glucosidosucrase; maltase-glucoamylase; alpha-glucopyranosidase; glucosidoinvertase; alpha-D-glucosidase; alpha-glucoside hydrolase; alpha-1,4-glucosidase; alpha-D-glucoside glucohydrolase. Cat No: NATE-1163. | |
| Native Microorganism α-Glucosidase (MALTASE) | Glycoside hydrolases (also called glycosidases or glycosyl hydrolases) assist in the hydrolysis of glycosidic bonds in complex sugars. They are extremely common enzymes with roles in nature including degradation of biomass such as cellulose and hemicellulose, in anti-bacterial defense strategies (e.g., lysozyme), in pathogenesis mechanisms (e.g., viral neuraminidases) and in normal cellular function (e.g., trimming mannosidases involved in N-linked glycoprotein biosynthesis). Together with glycosyltransferases, glycosidases form the major catalytic machinery for the synthesis and breakage of glycosidic bonds. Applications: This enzyme is useful for structural investi...tase; alpha-D-glucosidase; alpha-glucoside hydrolase; alpha-1,4-glucosidase; alpha-D-glucoside glucohydrolase; glycosidases; glycosyl hydrolases; α-Glucosidase. Enzyme Commission Number: EC 3.2.1.20. CAS No. 9001-42-7. Activity: 20U/mg-solid or more. Appearance: White amorphous powder, lyophilized. Form: Freeze dried powder. Source: Microorganism. Alpha-glucosidase; EC 3.2.1.20; maltase; glucoinvertase; glucosidosucrase; maltase-glucoamylase; alpha-glucopyranosidase; glucosidoinvertase; alpha-D-glucosidase; alpha-glucoside hydrolase; alpha-1,4-glucosidase; alpha-D-glucoside glucohydrolase; glycosidases; glycosyl hydrolases; α-Glucosidase. Cat No: DIA-194. | |
| Native Rice α-Glucosidase | Alpha-glucosidase is a glucosidase located in the brush border of the small intestine that acts upon 1,4-alpha bonds. This is in contrast to beta-glucosidase. Alpha-glucosidase breaks down starch and disaccharides to glucose. Maltase, a similar enzyme that cleaves maltose, is nearly functionally equivalent. The enzyme catalyses the hydrolyzis of a-1.6 linked a-galactose residues from oligosaccharides. Group: Enzymes. Synonyms: Alpha-glucosidase; EC 3.2.1.20; maltase; glucoinvertase; glucosidosucrase; maltase-glucoamylase; alpha-glucopyranosidase; glucosidoinvertase; alpha-D-glucosidase; alpha-glucoside hydrolase; alpha-1,4-glucosidase; alpha-D-glucoside glucohydrolase. Enzyme Commission Number: EC 3.2.1.20. CAS No. 9001-42-7. α-Glucosidase. Source: Rice. Alpha-glucosidase; EC 3.2.1.20; maltase; glucoinvertase; glucosidosucrase; maltase-glucoamylase; alpha-glucopyranosidase; glucosidoinvertase; alpha-D-glucosidase; alpha-glucoside hydrolase; alpha-1,4-glucosidase; alpha-D-glucoside glucohydrolase. Cat No: NATE-0041. | |
| Native Saccharomyces cerevisiae α-Glucosidase | Alpha-glucosidase is a glucosidase located in the brush border of the small intestine that acts upon 1,4-alpha bonds. This is in contrast to beta-glucosidase. Alpha-glucosidase breaks down starch and disaccharides to glucose. Maltase, a similar enzyme that cleaves maltose, is nearly functionally equivalent. Protein determined by biuret. Applications: For the determination of α-amylase and the synthesis of various 1?-o-sucrose and 1-o-fructose esters. α-glucosidase is used for the determination of α-amylase and the synthesis of various 1?-o-sucrose and 1-o-fructose esters. it was also used in the measurement of glycosidase inhibition. Group: Enzymes. Synonyms: α-glucosidase; maltase; glucoinvertase; glucosidosucrase; maltase-glucoamylase; α-glucopyranosidase; glucosidoinve. Enzyme Commission Number: EC 3.2.1.20. CAS No. 9001-42-7. α-Glucosidase. Mole weight: Mr ~63 kDa. Activity: 4-8 units/mg; > 10 units/mg protein (using p-nitrophenyl α-D-glucoside as substrate.). Storage: -20°C. Form: lyophilized powder. Source: Saccharomyces cerevisiae. α-glucosidase; maltase; glucoinvertase; glucosidosucrase; maltase-glucoamylase; α-glucopyranosidase; glucosidoinvertase; α-D-glucosidase; α-glucoside hydrolase; α-1,4-glucosidase; EC 3.2.1.20; 9001-42-7. Cat No: NATE-0752. | |
| Oligo-α-1,6-Glucosidase 13A from Bacillus cereus, Recombinant | Sucrase-isomaltase is a glucosidase enzyme located in on the brush border of the small intestine with system name oligosaccharide 6-alpha-glucohydrolase. Sucrase-isomaltase is a type II transmembrane glycoprotein located in the brush border of the small intestine. It has preferential expression in the apical membranes of enterocytes. The enzyme's purpose is to digest dietary carbohydrates such as starch, glucose, and isomaltose. By further processing the broken-down products, energy in the form of ATP can be generated. Group: Enzymes. Synonyms: EC 3.2.1.10; oligo-1,6-glucosidase; limit dextrinase; isomaltase; exo-oligo-1,6-glucosidase; dextrin 6alpha-glucanohydrolase; . Enzyme Commission Number: EC 3.2.1.10. Purity: >90% by SDS-PAGE. Oligo-1,6-Glucosidase. Mole weight: 67.8 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus cereus. EC 3.2.1.10; oligo-1,6-glucosidase; limit dextrinase; isomaltase; exo-oligo-1,6-glucosidase; dextrin 6alpha-glucanohydrolase; alpha-limit dextrinase; dextrin 6-glucanohydrolase; oligosaccharide alpha-1,6-glucohydrolase; Sucrase-isomaltase; Oligo-1,6-α-Glucosidase 13A. Cat No: NATE-1446. | |
| Oligo-α-1,6-Glucosidase 13A from Bifidobacterium adolescentis, Recombinant | Sucrase-isomaltase is a glucosidase enzyme located in on the brush border of the small intestine with system name oligosaccharide 6-alpha-glucohydrolase. Sucrase-isomaltase is a type II transmembrane glycoprotein located in the brush border of the small intestine. It has preferential expression in the apical membranes of enterocytes. The enzyme's purpose is to digest dietary carbohydrates such as starch, glucose, and isomaltose. By further processing the broken-down products, energy in the form of ATP can be generated. Group: Enzymes. Synonyms: EC 3.2.1.10; oligo-1,6-glucosidase; limit dextrinase; isomaltase; exo-oligo-1,6-glucosidase; dextrin. Enzyme Commission Number: EC 3.2.1.10. Purity: >90% by SDS-PAGE. Oligo-1,6-Glucosidase. Mole weight: 68.6 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bifidobacterium adolescentis. EC 3.2.1.10; oligo-1,6-glucosidase; limit dextrinase; isomaltase; exo-oligo-1,6-glucosidase; dextrin 6alpha-glucanohydrolase; alpha-limit dextrinase; dextrin 6-glucanohydrolase; oligosaccharide alpha-1,6-glucohydrolase; Sucrase-isomaltase; Oligo-1,6-α-Glucosidase 13A. Cat No: NATE-1447. | |
| 1,2:5,6-Di-O-isopropylidene-a-L-glucofuranose | 1,2:5,6-Di-O-isopropylidene-a-L-glucofuranose is an organic compound used in biomedical research, particularly in the development of anti-diabetic drugs. It plays a pivotal role in creating inhibitors for the enzyme alpha-glucosidase. Synonyms: α-L-Glucofuranose, 1,2:5,6-bis-O-(1-methylethylidene)-; (3aS,5R,6R,6aS)-5-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-ol; 1-O,2-O:5-O,6-O-Diisopropylidene-alpha-L-glucofuranose. Grades: ≥97%. CAS No. 79943-22-9. Molecular formula: C12H20O6. Mole weight: 260.28. |  |
| 1,2-Dideoxy-2-fluoro-galactonojirimycin | 1,2-Dideoxy-2-fluoro-galactonojirimycin, an alpha-glucosidase inhibitor, stands as an essential pharmacological agent for addressing Pompe disease - a lysosomal storage disorder characterized by massive glycogen buildup in tissues leading to muscle and organ failure. Through its inhibitory effect, this drug curbs glycogen accumulation in lysosomes, ultimately preventing muscle and tissue damage. Its clinical significance in the treatment of the disorder cannot be overemphasized. Synonyms: 2-F-DGJ. Molecular formula: C6H12NO3F. Mole weight: 165.16. | |
| 1,2-Dideoxy-2-piperidin-1-yl-a-D-glucopyranoso-[2,1-d]-2-thiazoline | 2-Thiazoline-alpha-D-glucopyranoso-[2,1-d]-1-yl-piperidin-2-dideoxy has been extensively employed in the biomedical sector as a potent glycosidase enzyme inhibitor, primarily alpha-glucosidases. The broad variation in sentence length and perplexity that characterizes the informative description of this compound underscores its potential therapeutic value for the treatment of diabetes and glycogen storage disease. | |
| 1,4-Dideoxy-1,4-imino-D-xylitol HCl | 1,4-Dideoxy-1,4-imino-D-xylitol HCl is a pharmaceutical compound used in the treatment of diabetes. It acts as an inhibitor of alpha-glucosidases, reducing the breakdown of complex carbohydrates into simple sugars. By slowing down carbohydrate absorption, it helps control blood glucose levels, thereby managing diabetes. Synonyms: (2R,3S,4S)-2-(Hydroxymethyl)pyrrolidine-3,4-diol hydrochloride; 186759-56-8; 1,4-dideoxy-1,4-imino-d-xylitol hydrochloride; 52019-89-3; 101399-04-6; (2R,3S,4S)-2-(hydroxymethyl)pyrrolidine-3,4-diol; hydrochloride; SCHEMBL2562496; W-202962; (2R,3S,4S)-2-(Hydroxymethyl)pyrrolidine-3,4-diolhydrochloride. CAS No. 52019-89-3. Molecular formula: C5H11NO3.HCl. Mole weight: 169.61. | |
| 1-(4-methoxy-phenoxy)-a-D-talopyranose | 1-(4-methoxy-phenoxy)-α-D-talopyranose is an intricate chemical compound, highly sought-after in the biomedical sector for its unparalleled therapeutic potential. It plays a pivotal role in treating complex disorders such as diabetes and cancer, acting as an alpha-glucosidase inhibitor that regulates blood glucose levels in patients with diabetes. In preclinical studies, this compound has demonstrated excellent antiproliferative properties and has emerged as a promising candidate in impeding the growth and metastasis of cancer cells. | |
| 1,5,6,7-Tetra-O-benzylvoglibose | 1,5,6,7-Tetra-O-benzylvoglibose, a carbohydrate-derived substance employed in the field of biomedicine, has been exhaustively researched due to its potential as an anti-diabetic medication in the fight against type 2 diabetes. This compound is ingeniously engineered to obstruct alpha-glucosidase enzymes, which play a critical role in carbohydrate digestion. Its ability to curtail postprandial blood glucose levels is a promising therapeutic choice in the management of type 2 diabetes. Synonyms: TBV. CAS No. 115250-39-0. Molecular formula: C38H45NO7. Mole weight: 627.77. | |
| 1,5-Anhydro-4,6-O-benzylidene-2-O-toluoyl-D-glucitol | 1,5-Anhydro-4,6-O-benzylidene-2-O-toluoyl-D-glucitol, a chemical compound praised for its antidiabetic properties, is typically utilized as a key ingredient in the development of groundbreaking medications. This compound facilitates effective glucose management by selectively targeting alpha-glucosidase enzymes, an important regulatory mechanism for optimal blood sugar levels in the body of patients afflicted with diabetes. CAS No. 156715-23-0. Molecular formula: C21H22O6. Mole weight: 370.4. | |
| 1,5-Anhydro-4,6-O-benzylidene-3-O-[2,4-dichlorophenyl]thiocarbonyloxy-2-O-toluoyl-D-glucitol | 1,5-Anhydro-4,6-O-benzylidene-3-O-[2,4-dichlorophenyl]thiocarbonyloxy-2-O-toluoyl-D-glucitol, a novel compound, has shown potent inhibition of alpha-glucosidase enzymes, making it a promising candidate for diabetes therapy. By reducing carbohydrate absorption, it is expected to effectively lower blood glucose levels. Its potential as a therapeutic agent for type 2 diabetes warrants further investigation, given its unique chemical profile and mechanism of action. Molecular formula: C28H24Cl2O7S. Mole weight: 575.46. | |
| 1,5-Dideoxy-1,5-imino-D-xylitol | 1,5-Dideoxy-1,5-imino-D-xylitol - a prospective remedial agent enlisted for the management of diabetes, corpulence and hypertension. It acts as an alpha-glucosidase inhibitor that curtails the hydrolysis and assimilation of carbohydrates, eventually leading to lower plasma glucose levels and refined insulin sensitivity. Furthermore, it possesses noteworthy efficacy in diminishing lipid deposition and augmenting hepatic functioning, as evidenced by various studies. Molecular formula: C5H11NO3. Mole weight: 133.15. | |
| 1-Deoxy-2-fluoronojirimycin | 1-Deoxy-2-fluoronojirimycin is a pharmacological therapy available for patients suffering from type 1 Gaucher disease. This rare genetic ailment is known to result in the accumulation of lipids within a few vital organs and tissues. Inhibiting enzyme alpha-glucosidase, which plays a crucial role in breaking down intricate sugars, is the primary mechanism of action of this drug. By obstructing the enzymatic activity, 1-Deoxy-2-fluoronojirimycin effectively mitigates lipid buildup, thereby enhancing the symptoms of Gaucher's disease. Molecular formula: C6H12FNO4. Mole weight: 181.16. | |
| 2,3-Anhydro-4,6-O-benzylidene-N-Boc-1,5-deoxy-1,5-imino-D-glucitol | 2,3-Anhydro-4,6-O-benzylidene-N-Boc-1,5-deoxy-1,5-imino-D-glucitol is a promising biomolecule with significant therapeutic potential for treating diabetes and related complications. This compound is noted for its capacity for inhibiting alpha-glucosidase, an enzyme pivotal in carbohydrate metabolism, which culminates in the reduction of postprandial glucose levels. The utilization of this molecule has the potential to revolutionize diabetes treatment and improve patient outcomes, with its multifaceted properties demonstrating hope for the future of diabetic management. Molecular formula: C18H23NO5. Mole weight: 333.38. | |
| 2,5-Anhydro-D-glucitol-1,6-bis-(dibenzylphosphate) | 2,5-Anhydro-D-glucitol-1,6-bis-(dibenzylphosphate), an intriguing molecule, presents itself as an eminent prospect with potential therapeutic properties for diabetes. This molecule portrays itself as an alpha-glucosidase inhibitor, curbing the carbohydrate breakdown which leads to glucose production. With this enzyme in check, postprandial hyperglycemia, an issue that is widely prevalent in diabetic patients, can be controlled. Furthermore, the multifunctional molecule, primarily built for diabetes control, exhibits enormous anti-inflammatory and antioxidant properties. The presence of these properties makes this molecule, with its potential benefits, a pivotal element for managing developed diabetic complications. Synonyms: dibenzyl [ (2S, 3R, 5R)-5-[bis (phenylmethoxy)phosphoryloxymethyl]-3, 4-dihydroxyoxolan-2-yl]methyl phosphate. Molecular formula: C34H38O11P2. Mole weight: 684.61. | |
| 2,5-Dideoxy-2,5-imino-L-mannitol | 2,5-Dideoxy-2,5-imino-L-mannitol is a compound used in the research of type 2 diabetes. It acts as an alpha-glucosidase inhibitor, reducing the breakdown and absorption of carbohydrates. This compound, derived from L-mannitol, interacts with specific enzymes involved in glucose metabolism. Synonyms: DMDP; 2R,5R-Bis(hydroxylmethyl)-(3R,4R)-dihydroxypyrrolidine,; (2R,3R,4R,5R)-2,5-β(hydroxymethyl)pyrrolidine-3,4-diol; L-DMDP; (2R,3R,4R,5R)-3,4-Dihydroxy-2,5-pyrrolidinedimethanol; NSC613239; D-Mannitol, 2,5-dideoxy-2,5-imino-, (6R-(6alpha,7alpha,7(R*)))-. Grades: ≥98%. CAS No. 59920-31-9. Molecular formula: C6H13NO4. Mole weight: 163.17. | |
| 2-Acetamido-4,6-O-benzylidene-N-(tert-butoxycarbonyl)-1,2,5-trideoxy-1,5-imino-D-glucitol | 2-Acetamido-4,6-O-benzylidene-N-(tert-butoxycarbonyl)-1,2,5-trideoxy-1,5-imino-D-glucitol is a synthetic compound used in the biomedical industry for treating type 2 diabetes. It works by inhibiting alpha-glucosidase, an enzyme that breaks down carbohydrates in the small intestine, slowing down the absorption of glucose and reducing blood sugar level. Synonyms: 2-ACETAMIDO-4,6-O-BENZYLIDENE-N-(TERT-BUTOXYCARBONYL)-1,2,5-TRIDEOXY-1,5-IMINO-D-GLUCITOL; tert-butyl (4aR,7S,8R,8aR)-7-acetamido-8-hydroxy-2-phenyl-4,4a,6,7,8,8a-hexahydro-[1,3]dioxino[5,4-b]pyridine-5-carboxylate; tert-Butyl (4aR,7S,8R,8aR)-7-acetamido-8-hydroxy-2-phenylhexahydro-5H-[1,3]dioxino[5,4-b]pyridine-5-carboxylate; starbld0032901; DTXSID00565023; tert-Butyl (4aR,7S,8R,8aR)-7-acetamido-8-hydroxy-2-phenylhexahydro-2H,5H-[1,3]dioxino[5,4-b]pyridine-5-carboxylate. CAS No. 1221795-90-9. Molecular formula: C20H28N2O6. Mole weight: 392.45. | |
| 2-Amino-2-deoxy-glucitol | 2-Amino-2-deoxy-glucitol, also known as miglitol, is a pharmacological agent used in the management of hyperglycemia associated with type 2 diabetes mellitus. Its mechanism of action involves the inhibition of alpha-glucosidase enzymes responsible for the breakdown of carbohydrates in the small intestine. This leads to a delay in the absorption of glucose, resulting in lower postprandial blood glucose levels. Despite its efficacy, miglitol may cause gastrointestinal side effects such as flatulence and diarrhea and is best used in combination with other antidiabetic agents. Synonyms: 5-aminohexane-1,2,3,4,6-pentol; 2351-14-6; SCHEMBL3797037; DTXSID60313360; NSC269409; NSC-269409. CAS No. 2351-14-6. Molecular formula: C6H15NO5. Mole weight: 181.19. | |
| 2-Naphthyl a-D-glucopyranoside | 2-Naphthyl a-D-glucopyranoside is a prominent compound compound, serving as a fundamental substrate in enzymatic assays, facilitating the quantification of distinct enzyme activities. Its primary application lies in evaluating glucosidase or glycosidase activities. Esteemed for its pivotal role in investigating pharmaceutical remedies concerning glycosidase anomalies, especially those connected to lysosomal storage ailments and various metabolic dysfunctions, this compound remains invaluable in scientific research and development. Synonyms: 2-Naphthyl alpha-D-glucopyranoside; 2-Naphthylglucoside; 2-NAPHTHYL-ALPHA-D-GLUCOPYRANOSIDE; beta-Naphthyl alpha-D-Glucopyranoside; (2R,3S,4S,5R,6R)-2-(Hydroxymethyl)-6-(naphthalen-2-yloxy)tetrahydro-2H-pyran-3,4,5-triol; A-D-GLUCOPYRANOSIDE,2-NAPHTHALENYL; 2-naphthyl alpha-D-glucoside; (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-naphthalen-2-yloxyoxane-3,4,5-triol; EINECS 246-834-0; 2-naphthyl-glucoside; 2-naphthyl-beta-D-glucoside; Naphthalen-2-yl hexopyranoside; b-Naphthyl a-D-Glucopyranoside; SCHEMBL1378657; beta-Naphthyl-alpha-D-glucoside; NIOSH/LZ5984300; CHEBI:90256; DTXSID50948165; AMY41707; 2-Naphthyl I+/--D-glucopyranoside; MFCD00067170; AKOS022171743; naphthalen-2-yl alpha-D-glucopyranoside; 1-(2-Naphthyl)-alpha-D-glucopyranoside; CS-0450103; LZ59843000; Glucopyranoside, 1-(2-naphthyl)-, alpha-D-; Q27162432; (2R,3R,4S,5R)-2-(hydroxymethyl)-6-naphthalen-2-yloxyoxane-3,4,5-triol; (2R,3S,4S,5R,6R)-2-(HYDROXYMETHYL)-6-(NAPHTHALEN-2-YLOXY)OXANE-3,4,5-TRIOL. CAS No. 25320-79-0. Molecular formula: C16H18O6. Mole weight: 306.31. | |
| 2-O-a-D-Galactopyranosyl-1-deoxynojirimycin | 2-O-a-D-Galactopyranosyl-1-deoxynojirimycin is an immensely influential compound, standing as a paramount and discerning force in inhibiting alpha-glucosidase enzymes. Synonyms: Galactosyl-DNJ. CAS No. 155168-05-1. Molecular formula: C12H23NO9. Mole weight: 325.31. | |
| 4-Methylumbelliferyl 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetamido-a-D-glucopyranoside | 4-Methylumbelliferyl 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetamido-a-D-glucopyranoside, a chemical compound widely employed in the biomedical industry, exhibits remarkable versatility in numerous applications. This compound, esteemed for its indispensability, finds significant utility in drug discovery and development processes, primarily serving as an essential substrate for enzymatic activity assays. Its unparalleled efficacy in detecting and quantifying glucosidases propels the advancement of pharmaceutical research. Synonyms: 4-Methylumbelliferyl3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetamido-a-D-glucopyranoside; [(2R,3S,4R,5R,6R)-3,4-diacetyloxy-6-(4-methyl-2-oxochromen-7-yl)oxy-5-[(2,2,2-trifluoroacetyl)amino]oxan-2-yl]methyl acetate; (2R,3S,4R,5R,6R)-2-(Acetoxymethyl)-6-((4-methyl-2-oxo-2H-chromen-7-yl)oxy)-5-(2,2,2-trifluoroacetamido)tetrahydro-2H-pyran-3,4-diyl diacetate; 4-METHYLUMBELLIFERYL 2-TRIFLUOROACETYL-3,4,6-O-TRIACETYL-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE; MGLRSUPYLXVODY-FYKMYLNBSA-N; 2-Nitrophenyl b-D-glucuronide; DTXSID00745388; 4-Methylumbelliferyl 2-Trifluoroacetyl-3,4,6-O-triacetyl-2-deoxy-?-D-glucopyranoside; 4-Methylumbelliferyl 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetamido-a-D-glucopyranoside; W-201159; [(2R,3S,4R,5R,6R)-3,4-bis(acetyloxy)-6-[(4-methyl-2-oxo-2H-chromen-7-yl)oxy]-5-(2,2,2-trifluoroacetamido)oxan-2-yl]methyl acetate; 4-Methyl-2-oxo-2H-1-benzopyran-7-yl 3,4,6-tri-O-acetyl-2-deoxy-2-(2,2,2-trifluoroacetamido)-alpha-D-glucopyranoside. CAS No. 137686-92-1. Molecular formula: C24H24F3NO11. Mole weight: 559.44. | |
| 4-Methylumbelliferyl a-D-glucopyranoside | It is a fluorogenic substrate in the assay of a-glucosidase. Synonyms: 7-(α-D-Glucopyranosyloxy)-4-methyl-2H-1-benzopyran-2-one; 7-(α-D-Glucopyranosyloxy)-4-methyl-coumarin; 4-Methylumbelliferyl α-D-Glucose; 4-MU-alpha-D-glucoside; 4-Methyl-7-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2H-chromen-2-one; 2H-1-Benzopyran-2-one, 7-(a-D-glucopyranosyloxy)-4-methyl-. Grades: ≥95%. CAS No. 17833-43-1. Molecular formula: C16H18O8. Mole weight: 338.31. | |
| 4-Nitrophenyl 6-deoxy-6-(2-pyridylamino)-a-D-penta-(1-4)-glucopyranoside | 4-Nitrophenyl 6-deoxy-6-(2-pyridylamino)-α-D-penta-(1-4)-glucopyranoside is a versatile chemical compound exemplifying its significance lies in the realm of glucosidase inhibitors and the revolutionary field of carbohydrate-based drug design. With its exceptional structure, this compound unveils a gateway to unraveling the enigmatic pathologies associated with enzyme functionality and carbohydrate metabolism. Synonyms: (2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-6-[(2S,4R,5R,6S)-6-[(2R,3S,4R,5R,6R)-6-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-(4-nitrophenoxy)oxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-2,4,5-trihydroxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-[2-(pyridin-2-ylamino)ethyl]oxane-3,4,5-triol; 4-Nitrophenyl-O-6-deoxy-6-((2-pyridyl)amino)-alpha-D-glucopyranosyl-(1-4)-O-alpha-D-glucopyranosyl-(1-4)-O-alpha-D-glucopyranosyl-(1-4)-O-alpha-D-glucopyranosyl-(1-4)-alpha-D-glucopyranoside; alpha-D-Glucopyranoside, 4-nitrophenyl O-6-deoxy-6-(2-pyridinylamino)-alpha-D-glucopyranosyl-(1-4)-O-alpha-D-glucopyranosyl-(1-4)-O-alpha-D-glucopyranosyl-(1-4)-O-alpha-D-glucopyranosyl-(1-4)-. CAS No. 100111-14-6. Molecular formula: C41H59N3O27. Mole weight: 1025.91. | |
| 4-Nitrophenyl a-D-maltopyranoside | 4-Nitrophenyl a-D-maltopyranoside, a valuable biochemical substrate, has been employed in various analytical studies of alpha-glucosidases from different sources, namely yeast, plants, and bacteria, offering insight into their substrate specificities. This versatile compound can also serve as a powerful tool for identifying inhibitors targeting alpha-glucosidase and glucosidase-related activities. Synonyms: PG2. CAS No. 17400-77-0. Molecular formula: C18H25NO13. Mole weight: 463.39. | |
| 6-a-D-Maltotriosyl-maltotriose | 6-a-D-Maltotriosyl-maltotriose is a compound used in the research of diabetes and related metabolic disorders derived from maltose and acting as a potent inhibitor of alpha-glucosidase enzymes, slowing down the digestion and absorption of complex carbohydrates. Synonyms: Glc(a1-4)Glc(a1-4)Glc(a1-6)Glc(a1-4)Glc(a1-4)Glc; alpha-D-gluco-hexopyranosyl-(1->4)-alpha-D-gluco-hexopyranosyl-(1->4)-alpha-D-gluco-hexopyranosyl-(1->6)-alpha-D-gluco-hexopyranosyl-(1->4)-alpha-D-gluco-hexopyranosyl-(1->4)-D-gluco-hexopyranose. Molecular formula: C36H62O31. Mole weight: 990.86. | |
| Acarbose | Acarbose (BAY g 5421), antihyperglycemic agent, is an orally active alpha-glucosidase inhibitor ( IC 50 =11 nM). Acarbose can potentiate the hypoglycemic effects of sulfonylureas or insulin [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: BAY g 5421. CAS No. 56180-94-0. Pack Sizes: 10 mM * 1 mL; 200 mg; 1 g. Product ID: HY-B0089. |  |
| Acarbose | Acarbose is an inhibitor of alpha-glucosidase isolated from Actinoplance sp., used to treat type 2 diabetes. Uses: Enzyme inhibitors; hypoglycemic agents. Synonyms: Amylostatin J; Bay g 5421; α-GHI; Glucobay; 4,6-dideoxy-4-{[(1S,4S,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl]amino}-alpha-D-glucopyranosyl-(1?4)-alpha-D-glucopyranosyl-(1?4)-beta-D-glucopyranose. Grades: >95% by HPLC. CAS No. 56180-94-0. Molecular formula: C25H43NO18. Mole weight: 645.61. | |
| Acarbose sulfate | Acarbose sulfate is an anti-diabetic drug used to treat type 2 diabetes mellitus and, in some countries, prediabetes. It is an inhibitor of alpha glucosidase, an enteric enzyme that releases glucose from larger carbohydrates. Acarbose sulfate decreased the Fasting Blood Glucose of DM Rats. The fasting blood glucose (FBG) in the acarbose-treated group decreased significantly at week 2 (P<0.05), week 4 (P<0.05), week 6 (P<0.05), and week 8 (P<0.05) compared to the DM group. Synonyms: Bay-g 5421 sulfate; BAY g 5421 sulfate. Grades:>98%. CAS No. 1221158-13-9. Molecular formula: C25H45NO22S. Mole weight: 743.68. | |
| Acarbose tridecaacetate | Acarbose tridecaacetate - an alpha-glucosidase inhibitor utilized in managing type 2 diabetes mellitus, enables the delay in carbohydrate digestion and absorption, thus regulating postprandial glucose levels. Synonyms: O-2,3-Di-O-acetyl-4,6-dideoxy-4-[[4,5,6-tris(acetyloxy)-3-[(acetyloxy)methyl]-2-cyclohexen-1-yl]amino]-a-D-glucopyranosyl-(1-4)-O-2,3,6-tri-O-acetyl-a-D-glucopyranosyl-(1-4)-a-D-glucopyranose 1,2,3,6-tetraacetate. CAS No. 117065-98-2. Molecular formula: C51H69NO31. Mole weight: 1192.08. | |
| Acarviosin | Acarviosin is a potent pharmaceutical compound primarily employed in the research of diabetes and metabolic anomalies, exerts its effects through the remarkable inhibition of the enzymatic activity of alpha-glucosidase. Synonyms: [1S-(1a,4a,5b,6a)]-4,6-Dideoxy-4-[[4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-a-D-glucopyranoside methyl ester 4,6-Dideoxy-4-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-a-D-glucopyranoside methyl ester. CAS No. 80943-41-5. Molecular formula: C14H25NO8. Mole weight: 335.35. | |
| Alkaline Amylase for detergent | Alkaline amylase is a kind of alpha-amylase, incision glucosidase. It can hydrolyze starch into short chain dextrine and a small quantity of low molecular saccharide and rapidly reduce viscosity of starch. The function of alkaline amylase as follows: It can effectively decompose starch polysaccharide remains and remove dirt on fabric. Alkaline amylase can improve washing effect at 30°C. For better effect, alkaline amylase can be used with other detergents. Applications: It can effectively decompose starch polysaccharide remains and remove dirt on fabric. Group: Enzymes. Synonyms: Alkaline Amylase; for detergent; Alkaline amylase; reduce viscosity of starch; decompose starch polysaccharide remains; remove dirt; fabric; Detergent Enzymes; Detergents; Alkaline Amylase for detergent; DETE-2622. Alkaline Amylase. Appearance: powder or liquid. Alkaline Amylase; for detergent; Alkaline amylase; reduce viscosity of starch; decompose starch polysaccharide remains; remove dirt; fabric; Detergent Enzymes; Detergents; Alkaline Amylase for detergent; DETE-2622. Pack: 25kg/paper barrel (powder form), 30kg/polyster barrel (liquid form). Cat No: DETE-2622. | |
| α-Galactosidase, positionally specific from Escherichia coli, Recombinant | Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Activity using maltose as substrate at ph 6.0 at 25 deg c is ~2x > that obtained using p-nitrophenyl-α-d-glucoside as substrate at ph 6.8 at 37 oc. protein determined by biuret. Applications: Α-glucosidase is potential enzyme for the biosynthesis of complex carbohydrates. Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.22. CAS No. 9025-35-8. GLA. Activity: > 50 units/mg protein. Storage: 2-8°C. Form: Lyophilized powder containing potassium phosphate buffer salt. Source: E. coli. Species: Escherichia coli. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Cat No: NATE-0293. | |
| Amylase, gluco- | Synonyms: amyl oglucosidasefromaspergillusniger; AMYLOGLUCOSIDASE; AMYLOGLUCOSIDASE, ASPERGILLUS NIGER; ALPHA1,4-D-GLYCAN (GLUCOHYDROLASE); 1,4-ALPHA-D-GLUCAN GLUCOHYDROLASE; EC 3.2.1.3; GLUCOAMYLASE; EXO-1,4-ALPHA-GLUCOSIDASE. Grades: 95%. CAS No. 9032-08-0. Molecular formula: MFCD00081321. | |
| benzyl 2-acetamido-3-O-benzyl-2-deoxy-6-O-tosyl-α-D-glucopyranoside | Benzyl 2-acetamido-3-O-benzyl-2-deoxy-6-O-tosyl-α-D-glucopyranoside is a biochemical compound that is commonly used in biomedicine as a substrate for β-glucosidase activity assays and is also used in carbohydrate research for the synthesis of oligosaccharides. It can also be used as a starting material for the preparation of glycosyl amino acids and glycopeptides as well as to study the kinetics of glucosidase inhibition. Synonyms: Benzyl 2-acetamido-3-O-benzyl-2-deoxy-6-O-[(4-methylphenyl)sulfonyl]-alpha-D-glucopyranoside. Grades: 98%. CAS No. 50908-12-8. Molecular formula: C29H33NO8S. Mole weight: 555.64. | |
| Bromoconduritol (Mixture of Isomers) (6-Bromo-3,4,5-trihydroxy Cyclohex-1-ene) | Bromoconduritol selectively inhibits mammalian alpha-glucosidase 2 (Glc2/Glc1 glucosidase in the glycoprotein processing pathway), yeast alpha-glucosidase, and some beta-glucosidases. It does not inhibit mammalian alpha-glucosidase 1 (Glc3-glucosidase) or mammalian Golgi mannosidase 1 (alpha-1,2-specific) in the glycoprotein processing pathway; the formation of lipid-linked oligosaccharide precursor (dolichol pyrphosphate oligosaccharide) and the transfer of lipid-linked oligosaccharide to proteins.Preparations in ice-cold H2O should be used immediately. The half-time for decomposition of bromoconduritol A (debromination) is 16 min (H2O, pH 7.3, 37°C). Under similar conditions, the half-life of bromoconduritol B is 2 mins. Group: Biochemicals. Alternative Names: 6-Bromo-3,4,5-trihydroxy Cyclohex-1-ene; 6-Bromo-4-cyclohexene-1,2,3-triol. Grades: Highly Purified. CAS No. 42014-74-4. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C?H?O?Br, Molecular Weight: 209.04. US Biological Life Sciences. |  Worldwide |
| Ceftezole sodium | Ceftezole sodium (CTZ sodium) is a broad-spectrum cephem antibiotic against many species of gram-positive and gram-negative bacteria. Ceftezole sodium (CTZ sodium) is an alpha-glucosidase inhibitor with in vivo anti-diabetic activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CTZ sodium. CAS No. 41136-22-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N7096. | |
| Deoxynojirimycin (DNJ) | Deoxynojirimycin inhibits mammalian glucosidase 1. As well, it inhibits intestinal and lysosmal alpha-glucosidases, beta-glucosidase from sweet almonds, pancreatic alpha-amylase and amyloglucosidase. Group: Biochemicals. Alternative Names: DNJ. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Deoxynojirimycin Hydrochloride (DNJ Hydrochloride) | Deoxynojirimycin inhibits mammalian glucosidase 1. As well, it inhibits intestinal and lysosmal alpha-glucosidases, beta-glucosidase from sweet almonds, pancreatic alpha-amylase and amyloglucosidase. Group: Biochemicals. Alternative Names: DNJ Hydrochloride. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Galactosyl isomaltol | Galactosyl isomaltol is a remarkable constituent employed in the biomedical field to study diabetes, emerging as an influential and discriminative suppressor of alpha-glucosidase, characterized by its origin from the organic compound isomaltol. Synonyms: 2-Acetyl-3-furyl-b-D-galactopyranoside. CAS No. 82756-28-3. Molecular formula: C12H16O8. Mole weight: 288.25. | |
| Genistein | Cell-permeable, reversible, substrate competitive tyrosine kinase inhibitor (including EGFR phosphorylation), implicated in almost all cell growth and proliferation signal cascades. Inhibitor of mammalian DNA topoisomerase II. Anticancer agent, inducing cell cycle arrest and apoptosis. Antiangiogenic agent, down-regulates the transcription of genes involved in controlling angiogenesis. Binds estrogen receptor beta. Can increase the rate of growth of some ER expressing breast cancers. Potent alpha-glucosidase inhibitor. Anthelmintic. Anti-diabetic. Activates nuclear receptors, oestrogen receptors and peroxisome proliferator-activated receptors (all PPAR isoforms) and it inhibits various enzyme activities. Inhibitor of GLUT4-mediated glucose uptake in 3T3-L1 adipocytes. Stimulator of autophagy vacuolization. Antioxidant. TRAIL sensitizer. Acts as an agonist at the GPR30 receptor. DNA methyltransferase inhibitor. Genistein exhibits synergistic antibacterial effects on MRSA. Group: Biochemicals. Alternative Names: NSC 36586; Baichanin A; Differenol A; 4',5,7-Trihydroxyisoflavone; 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one. Grades: Highly Purified. CAS No. 446-72-0. Pack Sizes: 10mg, 50mg, 250mg. Molecular Formula: C??H??O?. US Biological Life Sciences. | Worldwide |
| Glucoamylase 97A from Bacteroides thetaiotaomicron, Recombinant | Glucan 1,4-alpha-glucosidase is an enzyme located on the brush border of the small intestine with system name 4-alpha-D-glucan glucohydrolase. This enzyme catalyses the following chemical reaction:Hydrolysis0 of terminal (1->4)-linked alpha-D-glucose residues successively from non-reducing ends of the chains with release of beta-D-glucose. Most forms of the enzyme can rapidly hydrolyse 1,6-alpha-D-glucosidic bonds when the next bond in the sequence is 1,4. Group: Enzymes. Synonyms: glucoamylase; amyloglucosidase; γ-amylase; lysosomal α-glucosidase; acid maltase; exo-1,4-α-glucosidase; glucose amylase; γ-1,4-glucan glucohydrolase; acid . Enzyme Commission Number: EC 3.2.1.3. CAS No. 9032-08-0. Purity: >90% by SDS-PAGE. Glucoamylase. Mole weight: 84.0 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. glucoamylase; amyloglucosidase; γ-amylase; lysosomal α-glucosidase; acid maltase; exo-1,4-α-glucosidase; glucose amylase; γ-1,4-glucan glucohydrolase; acid maltase; 1,4-α-D-glucan glucohydrolase; EC 3.2.1.3; 9032-08-0; Glucoamylase 97A. Cat No: NATE-1308. | |
| L-Allono-1,4-lactone | L-Allono-1,4-lactone is a compound used in the research of diabetes by regulating blood glucose levels. It functions as an inhibitor of alpha-glucosidase enzyme, thus reducing carbohydrate breakdown and delaying sugar absorption. Synonyms: L-Allono-1,4-lactone; (3S,4R,5S)-5-[(1S)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-one; (3S,4R,5S)-5-((S)-1,2-Dihydroxyethyl)-3,4-dihydroxydihydrofuran-2(3H)-one; L-Allonic acid, gamma-lactone; DTXSID401318806. CAS No. 78184-43-7. Molecular formula: C6H10O6. Mole weight: 178.14. | |
| Luteolin (3',4',5,7-Tetrahydroxyflavone, Luteolol, BRN 0292084, C.I. Natural Yellow 2, Digitoflavone, Flacitran, Flavopurpol, Daphneflavonol, Argemexitin) | Anticancer and antimetastatic. alpha-Glucosidase inhibitor. Topoisomerase I Inhibitor. Apoptosis inducer. Anti-inflammatory. 15-Lipoxygenase (15-LOX) inhibitor. IL-6 production inhibitor. Fatty acid synthase (FAS) inhibitor. Antioxidant. Free radical scavenger. Antiadipogenic. PPAR-y. inhibitor. Neuroprotective. Monoamine transporter activator. Inhibitor of phosphodiesterases 1-5 (PDE1-5). PKC(e) and Src kinase inhibitor. HDAC inhibitor. Autophagy modulator. Phosphatidylinositol 3-kinase (PI3K) / Akt signaling inhibitor. p90 ribosomal S6 kinase (RSK1/RSK2) kinase activity inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 491-70-3. Pack Sizes: 5mg, 25mg. Molecular Formula: C15H10O6. US Biological Life Sciences. | Worldwide |
| Melibiulose | Melibiulose is an innovative compound product, designed with a focus on studying the chronic condition of diabetes mellitus. Acting as a potent enzyme inhibitor, it effectively targets and inhibits the activity of alpha-glucosidase. Synonyms: 6-O-(a-D-Galactopyranosyl)-D-fructofuranose; (2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-[[(2R,3S,4S)-3,4,5-trihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]methoxy]tetrahydropyran-3,4,5-triol. CAS No. 111188-56-8. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| Microbial Natural Product Library | A unique collection of 193 microbial natural products for high throughput screening (HTS) and high content screening (HCS); - Targets include alpha-glucosidase, beta-lactamase, TNF-alpha, HDAC, PKC, HSP90, etc. ; - Detailed compound information with structure, target, activity, IC50 value, and biological activity description; - Structurally diverse, medicinally active, and cell permeable; - NMR and HPLC/LCMS validated to ensure high purity and quality. Uses: Scientific use. Product Category: L6500. Categories: Microbial Natural Product Libraries. |  |
| Miglitol | Miglitol is an oral anti-diabetic drug. Uses: 1-deoxynojirimycin; analogs & derivatives; alpha-glucosidases; antagonists & inhibitors; enzyme inhibitors. Synonyms: Miglitol; Glyset. Grades: >98%. CAS No. 72432-03-2. Molecular formula: C8H17NO5. Mole weight: 207.22. | |
| Native Aspergillus niger Amyloglucosidase | Glucan 1,4-alpha-glucosidase is an enzyme located on the brush border of the small intestine with system name 4-alpha-D-glucan glucohydrolase. This enzyme catalyses the following chemical reaction:Hydrolysis0 of terminal (1->4)-linked alpha-D-glucose residues successively from non-reducing ends of the chains with release of beta-D-glucose. Most forms of the enzyme can rapidly hydrolyse 1,6-alpha-D-glucosidic bonds when the next bond in the sequence is 1,4. Stabilized with glucose. Applications: Amyloglucosidase from aspergillus niger is used to hydrolyze α-d-glucosides. it may be used in the brewing of beer and in the production of bread and juices. amyloglucosidase has been used to hydrolyze glycogen into glucose monomers in order to study lipid accumulation in skeletal muscle. Group: Enzymes. Synonyms: glucoamylase; amyloglucosidase; γ-amylase; lysosomal α-glucosidase; acid maltase; exo-1,4-α-glucosidase; g. Enzyme Commission Number: EC 3.2.1.3. CAS No. 9032-08-0. Glucoamylase. Activity: > 300 U/mL. Form: aqueous solution. Source: Aspergillus niger. glucoamylase; amyloglucosidase; γ-amylase; lysosomal α-glucosidase; acid maltase; exo-1,4-α-glucosidase; glucose amylase; γ-1,4-glucan glucohydrolase; acid maltase; 1,4-α-D-glucan glucohydrolase; EC 3.2.1.3; 9032-08-0. Cat No: NATE-0075. | |
| Native Rhizopus sp. Amyloglucosidase | Glucan 1,4-alpha-glucosidase is an enzyme located on the brush border of the small intestine with system name 4-alpha-D-glucan glucohydrolase. This enzyme catalyses the following chemical reaction:Hydrolysis0 of terminal (1->4)-linked alpha-D-glucose residues successively from non-reducing ends of the chains with release of beta-D-glucose. Most forms of the enzyme can rapidly hydrolyse 1,6-alpha-D-glucosidic bonds when the next bond in the sequence is 1,4. Applications: Amyloglucosidase is used to hydrolyze α-d-glucosides. it may be used in the brewing of beer and in the production of bread and juices. amyloglucosidase, from rhizopus sp., has been used to study the cl...; amyloglucosidase; γ-amylase; lysosomal α-glucosidase; acid maltase; exo-1,4-α-glucosidase; glucose amylase; γ-1,4-glucan glucohydrolase; acid maltase; 1,4-α-D-glucan glucohydrolase; EC 3.2.1.3; 9032-08-0. Enzyme Commission Number: EC 3.2.1.3. CAS No. 9032-08-0. Glucoamylase. Activity: > 40,000 units/g solid. Storage: -20°C. Form: Lyophilized salt free powder. Source: Rhizopus sp. glucoamylase; amyloglucosidase; γ-amylase; lysosomal α-glucosidase; acid maltase; exo-1,4-α-glucosidase; glucose amylase; γ-1,4-glucan glucohydrolase; acid maltase; 1,4-α-D-glucan glucohydrolase; EC 3.2.1.3; 9032-08-0. Cat No: NATE-0076. | |
| Native Rhizopus sp. Glucoamylase | Glucan 1,4-alpha-glucosidase is an enzyme located on the brush border of the small intestine with system name 4-alpha-D-glucan glucohydrolase. This enzyme catalyses the following chemical reaction: Hydrolysis of terminal (1->4)-linked alpha-D-glucose residues successively from non-reducing ends of the chains with release of beta-D-glucose. Most forms of the enzyme can rapidly hydrolyse 1,6-alpha-D-glycosidic bonds when the next bond in the sequence is 1,4. Applications: This enzyme is useful for structural investigation of carbohydrates and for enzymatic determination of α-amylase when coupled with the related enzymes in clinical analysis. Group: Enzymes. Synonyms: EC 3.2.1.3; glucoamylase; amyloglucosidase; gamma-amylase; lysosomal alpha-glucosidase; acid maltase; exo-1,4-alpha-glucosidase; glucose amylase; gamma-1,4-glucan glucohydrolase; acid maltase; 1,4-alpha-D-glucan glucohydrolase. Enzyme Commission Number: EC 3.2.1.3. CAS No. 9032-08-0. Activity: 30U/mg-solid or more. Appearance: White amorphous powder (salt-free), lyophilized. Form: Freeze dried powder. Source: Rhizopus sp. EC 3.2.1.3; glucoamylase; amyloglucosidase; gamma-amylase; lysosomal alpha-glucosidase; acid maltase; exo-1,4-alpha-glucosidase; glucose amylase; gamma-1,4-glucan glucohydrolase; acid maltase; 1,4-alpha-D-glucan glucohydrolase. Cat No: DIA-190. | |
| Native Sweet almonds β-Glucosidase | β-glucosidase is a glucosidase enzyme located in on the brush border of the small intestine that acts upon β1->4 bonds linking two glucose or glucose-substituted molecules (i.e., the disaccharide cellobiose). It 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. Beta-glucosidase isolated from sweet almonds is used in the determination of alpha-amylase and in carbohydrate structure research. creative enzyme...9001-22-3. β-Glucosidase. Activity: > 1000 U/mg. Storage: Store desiccated at-15°C or below. Allow to come to room temperature before opening. Before returning to storage, redesiccate under vacuum over silica gel for a minimum of four hours. Re-seal before returning to-15°C or below. Form: A freeze-dried material. Source: Sweet almonds. β-glucosidase; glycoside hydrolase; β-D-glucoside glucohydrolase; EC 3.2.1.6; gentiobiase; cellobiase; emulsin; elaterase; aryl-β-glucosidase; β-D-glucosidase; arbutinase; amygdalinase; p-nitrophenyl β-glucosidase; primeverosidase; amygdalase; linamarase; salicilinase; β-1,6-glucosidase. Cat No: NATE-0770. | |
| Pellitorine | Cell-permeable. A natural product isolated from the roots of Piper Nigrum. Shows larvicidal, antimycobacterial and antituberculosis activity. Modulator of the sensory neuron function to induce tingling parethesia. Tingling-inducing agent. Excellent stable model compound for sensory studies. alpha-Glucosidase inhibitor used in diabetes mellitus, cancer, infection and inflammatory research. ACAT (Acyl-CoA cholesteryl acyl transferase) inhibitor. Potential anti-cancer lead compound. Source:Synthetic. Originally isolated from roots of Anacyclus pryrethrum and fruits of Piper nigrum. Group: Biochemicals. Alternative Names: (E,E)-N-(2-Methylpropyl) 2,4-decadienamide, BRN 1725967. Grades: Highly Purified. CAS No. 18836-52-7. Pack Sizes: 1mg, 5mg. Molecular Formula: C14H25NO, Molecular Weight: 223.4. US Biological Life Sciences. | Worldwide |
| SP-187 HCl | SP-187, also known as N-9-DNJ and UV-4B, is an alpha-Glucosidase inhibitor potentially for the treatment of dengue fever and influenza infection. Proline-producing strains of Serratia marcescens were more osmotolerant than wild-type strains. Growth inhibition by proline analogs was significantly enhanced by increasing the osmotic stress of the medium. Group: Inhibitors. Alternative Names: SP-187 HCl; SP-187 hydrochloride SP-187; SP187; SP 187; N-9-DNJ; UV-4B; N9DNJ; UV4B; N 9 DNJ; UV 4B; Iminosugar UV 4; MON-DNJ; N-9-Methoxynonyldeoxynojirimycin. CAS No. 1333144-07-2. Molecular formula: C16H34ClNO5. Mole weight: 355.9. Appearance: Solid powder. Purity: >98%. IUPACName: (2R,3R,4R,5S)-2-(hydroxymethyl)-1-(9-methoxynonyl)piperidine-3,4,5-triol hydrochloride. Canonical SMILES: O[C@@H]1[C@@H] (CO)N (CCCCCCCCCOC)C[C@H] (O)[C@H]1O. [H]Cl. Catalog: ACM1333144072. |  |
| Voglibose | Voglibose is an orally active alpha-glucosidase inhibitor that prevents the development of colorectal precancerous lesions induced by obesity and diabetes. Voglibose reduces oxidative stress in an inflammatory environment and inhibits the insulin-like growth factor/insulin-like growth factor-1 receptor (IGF/IGF-1R) functional axis [1]. Uses: Scientific research. Group: Natural products. CAS No. 83480-29-9. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B0025. | |
| Voglibose (3, 4-Dideoxy-4-[[2-hydroxy-1- (hydroxymethyl) ethyl]amino]-2-C- (hydroxymethyl) -D-epiinositol) | An alpha-Glucosidase inhibitor used as an antidiabetic. Group: Biochemicals. Alternative Names: 3, 4-Dideoxy-4-[[2-hydroxy-1- (hydroxymethyl) ethyl]amino]-2-C- (hydroxymethyl) -D-epiinositol. Grades: Highly Purified. CAS No. 83480-29-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
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