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| Product | Description | |
|---|---|---|
| D-Heptamannuronic Acid Heptasodium Salt | D-Heptamannuronic Acid Heptasodium Salt is a natural polysaccharide derived from the marine bacterium, presents itself as a sodium salt form in this product. Synonyms: Hepta-Mannuronic Acid Sodium Salt. Grades: ≥95% by GPC. Molecular formula: C42H51O43Na7. Mole weight: 1404.76. |  |
| Di-mannuronic acid sodium salt | Di-mannuronic acid sodium salt is an essential bioactive compound, used in studying inflammatory afflictions, including arthritand autoimmune diseases. Furthermore, its utilization extends to the research of cardiovascular disorders. Molecular formula: C12H16O13Na2. Mole weight: 414.23. | |
| D-mannuronic acid sodium | D-Mannuronic Acid Sodium Salt is a vital component used in the production of alginate hydrogels for drug delivery applications in biomedicine. It serves as a crosslinker, enhancing the stability and controlled release of various drugs to study conditions such as cancer, bacterial infections, and cardiovascular diseases. Synonyms: Sodium mannuronate; Sodium D-mannuronate; D-Mannuronic acid sodium salt. CAS No. 921-56-2. Molecular formula: C6H9NaO7. Mole weight: 216.12. | |
| D-Mannuronic acid sodium | D-Mannuronic acid sodium, isolated from Macrocystis pyrifera , has the potential in autoimmune encephalomyelitis (EAE), adjuvant induced arthritis (AIA), nephrotic syndrome, and acute glomerulonephritis studies [1]. Uses: Scientific research. Group: Natural products. CAS No. 921-56-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N7703. |  |
| D-Nonamannuronic Acid Nonasodium Salt | D-Nonamannuronic Acid Nonasodium Salt is a multifaceted biochemical compound, finding a multitude of applications, particularly in the production of potent antiviral drugs with exceptional efficacy against influenza A as well as B viruses. Synonyms: Nona-Mannuronic Acid Sodium Salt. Grades: ≥93% by GPC. Molecular formula: C54H65O55Na9. Mole weight: 1800.96. | |
| D-Octamannuronic Acid Octasodium Salt | D-Octamannuronic Acid Octasodium Salt is an extraordinary biomedical compound that exhibits remarkable potential in research of a myriad of ailments, including cardiovascular disorders and inflammation.This prodigious compound demonstrates promising efficacy against bacterial infections through its profound disruption of biofilm formation. Synonyms: Octa-Mannuronic Acid Sodium Salt. Grades: ≥94% by GPC. Molecular formula: C48H58O49Na8. Mole weight: 1602.86. | |
| Hexa-mannuronic acid sodium salt | Hexa-mannuronic acid sodium salt is a cutting-edge compound with remarkable anti-inflammatory activities, aiding in research of multifarious inflammatory disorders, including the complex pathologies of rheumatoid arthritand asthma. Molecular formula: C36H44O37Na6. Mole weight: 1206.65. | |
| Penta-mannuronic acid sodium salt | Penta-mannuronic acid sodium salt is an indispensable compound product, exhibiting remarkable efficacy in studying diverse ailments such as drug-resistant bacteria infections and inflammation-associated disorders like rheumatoid arthritis. Molecular formula: C30H37O31Na5. Mole weight: 1008.55. | |
| Tetra-mannuronic acid sodium salt | Tetra-mannuronic acid sodium salt is a promising compound, standing out as a tool for the research of an array of distressing inflammatory disorders, specifically encompassing the prolific rheumatoid arthritand ulcerative colitis. This extraordinary compound demonstrates profound immunomodulatory potential by effectively orchestrating cytokine production and transcendently inhibiting unwarranted inflammation. Molecular formula: C24H30O25Na4. Mole weight: 810.44. | |
| Tri-mannuronic acid sodium salt | Tri-mannuronic acid sodium salt is a paramount pharmaceutical compound, finding remarkable application in studying an array of maladies including cancer, inflammation and cardiovascular disorders. Notably, this compound has exceptional propensity to selectively engage intricate cellular pathways and control pertinent molecular mechanisms. Molecular formula: C18H23O19Na3. Mole weight: 612.33. | |
| D-Mannurono-6,3-lactone | D-Mannurono-6,3-lactone is an indispensable compound, acting as a precursor in vitamin C synthesis to augment collagen generation and facilitate the absorption of iron. Moreover is an exceptional attribute of D-Mannurono-6,3-lactone lies in its antioxidants capabilities, proficiently safeguarding cellular entities against the detrimental effects of oxidative burdens. P. Synonyms: D-Mannuronic acid lactone;D-Mannofuranuronic acid gamma-lactone. CAS No. 7424-9-1. Molecular formula: C6H8O6. Mole weight: 176.12. | |
| N-Acetyl-D-mannosaminuronic acid | Synonyms: Mannacua; N-Acetylmannosaminuronic acid; N-Acetyl-D-mannosaminuronic acid; 57496-35-2; 32TW3B2ZFO; Mannuronic acid, 2-acetamido-2-deoxy-; Mannuronic acid, 2-(acetylamino)-2-deoxy-; D-Mannuronic acid, 2-(acetylamino)-2-deoxy-; 32452-11-2; UNII-32TW3B2ZFO; SCHEMBL1311637; DTXSID40206105; 2-acetamido-2-deoxymannuronic acid; Q27256190. Molecular formula: C8H13NO7. Mole weight: 235.19. | |
| Sodium Mannuronate Methylsilanol | Use as emulsifying agent, dispersing agent. Group: Silicone surfactantsdispersing agentsemulsifying agents. Alternative Names: Mannuronic acid, monosodium salt, compd. with methylsilanetriol (1:1), D-. CAS No. 23732-95-8. Molecular formula: C7H13NaO7Si. Mole weight: 260.25. Catalog: ACM23732958. |  |
| UDP-2,3-diacetamido-2,3-dideoxyglucuronic acid 2-epimerase | This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of the B-band lipopolysaccharide of Pseudomonas aeroginosa serotype O5 and of the band-A trisaccharide of Bordetella pertussis, both important respiratory pathogens. The enzyme is highly specific as UDP-α-D-GlcNAc, UDP-α-D-GlcNAcA (UDP-2-acetamido-2-deoxy-α-D-glucuronic acid) and UDP-α-D-GlcNAc3NAc (UDP-2,3-diacetamido-2,3-dideoxy-α-D-glucose) cannot act as substrates. Group: Enzymes. Synonyms: UDP-GlcNAc3NAcA 2-epimerase; UDP-α-D-GlcNAc3NAcA 2-epimerase; 2,3-diacetamido-2,3-dideoxy-α-D-glucuronic acid 2-epimerase; WbpI; WlbD. Enzyme Commission Number: EC 5.1.3.23. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5409; UDP-2,3-diacetamido-2,3-dideoxyglucuronic acid 2-epimerase; EC 5.1.3.23; UDP-GlcNAc3NAcA 2-epimerase; UDP-α-D-GlcNAc3NAcA 2-epimerase; 2,3-diacetamido-2,3-dideoxy-α-D-glucuronic acid 2-epimerase; WbpI; WlbD. Cat No: EXWM-5409. |  |
| UDP-2-acetamido-2-deoxy-ribo-hexuluronate aminotransferase | A pyridoxal 5'-phosphate protein. This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of B-band lipopolysaccharide. The enzymes from Pseudomonas aeruginosa serotype O5 and Thermus thermophilus form a complex with the previous enzyme in the pathway, EC 1.1.1.335 (UDP-N-acetyl-2-amino-2-deoxyglucuronate oxidase). Group: Enzymes. Synonyms: WbpE; WlbC. Enzyme Commission Number: EC 2.6.1.98. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2939; UDP-2-acetamido-2-deoxy-ribo-hexuluronate aminotransferase; EC 2.6.1.98; WbpE; WlbC. Cat No: EXWM-2939. | |
| UDP-2-acetamido-3-amino-2,3-dideoxy-glucuronate N-acetyltransferase | This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of B-band lipopolysaccharide. Group: Enzymes. Synonyms: WbpD; WlbB. Enzyme Commission Number: EC 2.3.1.201. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2146; UDP-2-acetamido-3-amino-2,3-dideoxy-glucuronate N-acetyltransferase; EC 2.3.1.201; WbpD; WlbB. Cat No: EXWM-2146. | |
| UDP-N-acetyl-2-amino-2-deoxyglucuronate dehydrogenase | This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of B-band lipopolysaccharide. The enzymes from Pseudomonas aeruginosa serotype O5 and Thermus thermophilus form a complex with the the enzyme catalysing the next step the pathway (EC 2.6.1.98, UDP-2-acetamido-2-deoxy-ribo-hexuluronate aminotransferase). The enzyme also possesses an EC 1.1.99.2 (L-2-hydroxyglutarate dehydrogenase) activity, and utilizes the 2-oxoglutarate produced by EC 2.6.1.98 to regenerate the tightly bound NAD+. The enzymes from Bordetella pertussis and Chromobacterium violaceum do not bind NAD+ as tightly and do not require 2-oxoglutarate to function. Group: Enzymes. Synonyms: WlbA; WbpB. Enzyme Commission Number: EC 1.1.1.335. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0249; UDP-N-acetyl-2-amino-2-deoxyglucuronate dehydrogenase; EC 1.1.1.335; WlbA; WbpB. Cat No: EXWM-0249. | |
| UDP-N-acetylglucosamine 6-dehydrogenase | This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of B-band lipopolysaccharide. Group: Enzymes. Synonyms: uridine diphosphoacetylglucosamine dehydrogenase; UDP-acetylglucosamine dehydrogenase; UDP-2-acetamido-2-deoxy-D-glucose:NAD oxidoreductase; UDP-GlcNAc dehydrogenase; WbpA; WbpO. Enzyme Commission Number: EC 1.1.1.136. CAS No. 9054-83-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0040; UDP-N-acetylglucosamine 6-dehydrogenase; EC 1.1.1.136; 9054-83-5; uridine diphosphoacetylglucosamine dehydrogenase; UDP-acetylglucosamine dehydrogenase; UDP-2-acetamido-2-deoxy-D-glucose:NAD oxidoreductase; UDP-GlcNAc dehydrogenase; WbpA; WbpO. Cat No: EXWM-0040. | |
| Native Alginate Lyase | In enzymology, a poly (beta-D-mannuronate) lyase (EC 4.2.2.3) is an enzyme that catalyzes the chemical reaction:Eliminative cleavage of polysaccharides containing beta-D-mannuronate residues to give oligosaccharides with 4-deoxy-alpha-L-erythro-hex-4-enopyranuronosyl groups at their ends. This enzyme belongs to the family of lyases, specifically those carbon-oxygen lyases acting on polysaccharides. This enzyme participates in fructose and mannose metabolism. Applications: Alginate lyase is used to break down alginate or alginic acid and to reduce viscosity. it is useful during follicle isolation, encapsulation, and culture. Group: Enzymes. Synonyms: alginate lyase I; alginate lyase; alginase I; alginase II; alginase; poly (β-D-1,4-mannuronide) lyase; EC 4.2.2.3; 9024-15-1. Enzyme Commission Number: EC 4.2.2.3. CAS No. 9024-15-1. Alginate lyase. Activity: > 10,000 units/g solid. Storage: 2-8°C. Form: powder. alginate lyase I; alginate lyase; alginase I; alginase II; alginase; poly (β-D-1,4-mannuronide) lyase; EC 4.2.2.3; 40591-57-9. Cat No: NATE-0050. | |
| UDP-N-acetyl-D-mannosaminuronic acid | Synonyms: Udp-N-acetyl-D-mannosaminuronic acid; UDP-N-acetyl-alpha-D-mannosaminouronic acid; UDP-N-acetyl-2-amino-2-deoxy-D-mannuronate; uridine 5'-[3-(2-acetamido-2-deoxy-alpha-D-mannopyranosyluronic acid) dihydrogen diphosphate]; (2s,3s,4r,5s,6r)-5-Acetamido-6-[[[(2r,3s,4r,5r)-5-[2,4-Bis(Oxidanylidene)pyrimidin-1-Yl]-3,4-Bis(Oxidanyl)oxolan-2-Yl]methoxy-Oxidanyl-Phosphoryl]oxy-Oxidanyl-Phosphoryl]oxy-3,4-Bis(Oxidanyl)oxane-2-Carboxylic Acid; UDP-N-acetyl-alpha-D-mannosaminuronate; C06240; CHEBI:70738; (2S,3S,4R,5S,6R)-5-acetamido-6-[[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-3,4-dihydroxyoxane-2-carboxylic acid; J-700273; Q27139053; (2S, 3S, 4R, 5S, 6R)-5- (acetylamino)-6-{[ (R)-{[ (R)-{[ (2R, 3S, 4R, 5R)-5- (2, 4-dioxo-3, 4-dihydropyrimidin-1 (2H)-yl)-3, 4-dihydroxytetrahydrofuran-2-yl]methoxy} (hydroxy)phosphoryl]oxy} (hydroxy)phosphoryl]oxy}-3, 4-dihydroxytetrahydro-2H-pyran-2-carboxylic acid (non-preferred name); SAJ. Molecular formula: C17H25N3O18P2. Mole weight: 621.3. | |
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