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| Product | Description | |
|---|---|---|
| oligosaccharide 4-α-D-glucosyltransferase | The enzyme acts on amylose, amylopectin, glycogen and maltooligosaccharides. No detectable free glucose is formed, indicating the enzyme does not act as a hydrolase. The enzyme from the bacterium Cellvibrio japonicus has the highest activity with maltotriose as a donor, and also accepts maltose, while the enzyme from amoeba does not accept maltose. Oligosaccharides with 1?6 linkages cannot function as donors, but can act as acceptors. Unlike EC 2.4.1.25, 4-α-glucanotransferase, this enzyme can transfer only a single glucosyl residue. Group: Enzymes. Synonyms: amylase III; 1,4-α-glucan:1,4-α-glucan 4-α-glucosyltransferase; 1,4-α-D-glucan:1,4-α-D-glucan 4-α-D-glucosyltransferase; α-1,4-transglucosylase. Enzyme Commission Number: EC 2.4.1.161. CAS No. 9000-92-4. 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-2386; oligosaccharide 4-α-D-glucosyltransferase; EC 2.4.1.161; 9000-92-4; amylase III; 1,4-α-glucan:1,4-α-glucan 4-α-glucosyltransferase; 1,4-α-D-glucan:1,4-α-D-glucan 4-α-D-glucosyltransferase; α-1,4-transglucosylase. Cat No: EXWM-2386. |  |
| oligosaccharide-diphosphodolichol diphosphatase | This enzyme belongs to the family of hydrolases, specifically those acting on acid anhydrides in phosphorus-containing anhydrides. Group: Enzymes. Synonyms: oligosaccharide-diphosphodolichol pyrophosphatase. Enzyme Commission Number: EC 3.6.1.44. CAS No. 117698-28-9. 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-4621; oligosaccharide-diphosphodolichol diphosphatase; EC 3.6.1.44; 117698-28-9; oligosaccharide-diphosphodolichol pyrophosphatase. Cat No: EXWM-4621. | |
| Oligosaccharide dp20 | Oligosaccharide dp20, a valuable carbohydrate agent employed to tackle metabolic disorders and diabetes. Abiding by its distinctive mechanism of action - a likeness to insulin, it portrays its utility in regulating the levels of glucose in the bloodstream. The small molecular weight ensures effortless absorption in the body, resulting in efficacious utilization and nutrients replenishment. An ideal supplement for improving glucose imbalances, it also exhibits promising antioxidant and anti-inflammatory effects, hence presenting itself as an apt functional food ingredient. Synonyms: Heparin derived dp20 saccharide ammonium salt. Molecular formula: C120H150N10O190S33(NH4)44. Mole weight: 6624.25. |  |
| oligosaccharide reducing-end xylanase | The enzyme, originally isolated from the bacterium Bacillus halodurans C-125, releases the xylose unit at the reducing end of oligosaccharides ending with the structure β-D-xylopyranosyl-(1?4)-β-D-xylopyranosyl-(1?4)-β-D-xylopyranose, leaving the new reducing end in the α configuration. It is specific for the β anomers of xylooligosaccharides whose degree of polymerization is equal to or greater than 3.The penultimate residue must be β-D-xylopyranose, but replacing either of the flanking residues with glucose merely slows the rate greatly. Group: Enzymes. Synonyms: Rex; reducing end xylose-releasing exo-oligoxylanase. Enzyme Commission Number: EC 3.2.1.156. CAS No. 879497-03-7. Oligosaccharide reducing-end xylanase. 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-3839; oligosaccharide reducing-end xylanase; EC 3.2.1.156; 879497-03-7; Rex; reducing end xylose-releasing exo-oligoxylanase. Cat No: EXWM-3839. | |
| Oligosaccharide reducing-end xylanase 8A from Bacillus halodurans, Recombinant | Oligosaccharide reducing-end xylanase (EC 3.2.1.156, Rex, reducing end xylose-releasing exo-oligoxylanase) is an enzyme with systematic name beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranose reducing-end xylanase. This enzyme catalyses the following chemical reaction: Hydrolysis of (1->4)-beta-D-xylose residues from the reducing end of oligosaccharides. The enzyme acts rapidly on the beta-anomer of beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranose. Group: Enzymes. Synonyms: Oligosaccharide reducing-end xylanase; EC 3.2.1.156; Rex; reducing end xylose-releasing exo-oligoxylanase; beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranose reducing-end xylanase. Enzyme Commission Number: EC 3.2.1.156. CAS No. 879497-03-7. Purity: >90% as judged by SDS-PAGE. Oligosaccharide reducing-end xylanase. Mole weight: 47.1 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 halodurans. Oligosaccharide reducing-end xylanase; EC 3.2.1.156; Rex; reducing end xylose-releasing exo-oligoxylanase; beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranose reducing-end xylanase. Cat No: NATE-1515. | |
| Oligosaccharide reducing-end xylanase 8A from Bifidobacterium adolescentis, Recombinant | Oligosaccharide reducing-end xylanase (EC 3.2.1.156, Rex, reducing end xylose-releasing exo-oligoxylanase) is an enzyme with systematic name beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranose reducing-end xylanase. This enzyme catalyses the following chemical reaction: Hydrolysis of (1->4)-beta-D-xylose residues from the reducing end of oligosaccharides. The enzyme acts rapidly on the beta-anomer of beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranose. Group: Enzymes. Synonyms: Oligosaccharide reducing-end xylanase; EC 3.2.1.156; Rex; reducing end xylose-releasing exo-oligoxylanase; beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranose reducing-end xylanase. Enzyme Commission Number: EC 3.2.1.156. CAS No. 879497-03-7. Purity: >90% as judged by SDS-PAGE. Oligosaccharide reducing-end xylanase. Mole weight: 45.8 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: Bifidobacterium adolescentis. Oligosaccharide reducing-end xylanase; EC 3.2.1.156; Rex; reducing end xylose-releasing exo-oligoxylanase; beta-D-xylopyranosyl-(1->4)-beta-D-xylopyranose reducing-end xylanase. Cat No: NATE-1516. | |
| oligosaccharide-transporting ATPase | ABC-type (ATP-binding cassette-type) ATPase, characterized by the presence of two similar ATP-binding domains. Does not undergo phosphorylation during the transport process. A bacterial enzyme that imports lactose, melibiose and raffinose. Group: Enzymes. Enzyme Commission Number: EC 7.5.2.2 (Formerly EC 3.6.3.18). 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-4654; oligosaccharide-transporting ATPase; EC 3.6.3.18. Cat No: EXWM-4654. | |
| a-Glucan oligosaccharide | a-Glucan oligosaccharide, derived from yeast cell walls, is a polysaccharide with remarkable capacity in fortifying the immune system and serving as a prebiotic, fostering the proliferation of symbiotic microorganisms within the gastrointestinal tract. This natural compound finding valuable application in the biomedical realm, facilitating the development of functional nutraceuticals and alimentary addenda aimed at ameliorating gut wellbeing and augmenting the organism's resilience against pathogenic intruders. Synonyms: a-oligoglucan. CAS No. 27707-45-5. | |
| α-neoagaro-oligosaccharide hydrolase | When neoagarohexaose is used as a substrate, the oligosaccharide is cleaved at the non-reducing end to produce 3,6-anhydro-L-galactose and agaropentaose, which is further hydrolysed to agarobiose and agarotriose. With neoagarotetraose as substrate, the products are predominantly agarotriose and 3,6-anhydro-L-galactose. In Vibrio sp. the actions of EC 3.2.1.81,β-agarase and EC 3.2.1.159 can be used to degrade agarose to 3,6-anhydro-L-galactose and D-galactose. Group: Enzymes. Synonyms: α-neoagarooligosaccharide hydrolase; α-NAOS hydrolase. Enzyme Commission Number: EC 3.2.1.159. CAS No. 60063-77-6. 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-3842; α-neoagaro-oligosaccharide hydrolase; EC 3.2.1.159; 60063-77-6; α-neoagarooligosaccharide hydrolase; α-NAOS hydrolase. Cat No: EXWM-3842. | |
| Chito-oligosaccharides hydrochloride | Chito-oligosaccharides hydrochloride is an innovative biomedical compound boasting exceptional antimicrobial qualities, rendering it exceptionally efficacious in research of both bacterial and fungal infections. Consequently, Chito-oligosaccharides hydrochloride emerges as a formidable candidate for the research of gastritis, gastric ulcers and cutaneous maladies. Grades: ≥97% by HPLC. Molecular formula: (C6H13NO5·HCL)3-7. | |
| Chitosan oligosaccharide | Chitosan oligosaccharide (COS) is an oligomer of β-(1→4)-linked D-glucosamine. Chitosan oligosaccharide (COS) activates AMPK and inhibits inflammatory signaling pathways including NF-κB and MAPK pathways. Uses: Scientific research. Group: Natural products. Alternative Names: COS. CAS No. 148411-57-8. Pack Sizes: 500 mg; 1 g; 5 g. Product ID: HY-112108. |  |
| Chitosan oligosaccharide (COS) | Chitosan oligosaccharide (COS). Group: Polymers. CAS No. 148411-57-8. Product ID: (2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-2-(hydroxymethyl)oxane-3,4-diol. Molecular formula: 340.33g/mol. Mole weight: C12H24N2O9. C (C1C (C (C (C (O1)OC2C (OC (C (C2O)N)O)CO)N)O)O)O. InChI=1S/C12H24N2O9/c13-5-9 (19)10 (4 (2-16)21-11 (5)20)23-12-6 (14)8 (18)7 (17)3 (1-15)22-12/h3-12, 15-20H, 1-2, 13-14H2/t3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12+/m1/s1. QLTSDROPCWIKKY-PMCTYKHCSA-N. |  |
| Chitosan oligosaccharide HCl | Chitosan oligosaccharide lactate may be used in water treatment for organic and heavy metal pollutants, biomedical devices, biodegradable packaging, textile finishing for water permeable fabrics, cosmetics. Synonyms: Chitosan HCl. CAS No. 148411-57-8. Molecular formula: (C12H24N2O9)n. Mole weight: 340.33. | |
| Chitosan oligosaccharide lactate | Mn = 4,000 - 6,000. Uses: Chitosan oligosaccharide lactate may be used in water treatment for organic and heavy metal pollutants, biomedical devices, biodegradable packaging, textile finishing for water permeable fabrics, cosmetics. Group: Biodegradable polymers. CAS No. 148411-57-8. Pack Sizes: 1, 10 g in poly bottle. Product ID: (2R,3S,4R,5R,6S)-5-amino-6-[(2R,3S,4R,5R,6R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-2-(hydroxymethyl)oxane-3,4-diol. Molecular formula: average Mn 5,000. Mole weight: (C12H24N2O9)n. N[C@H]1[C@H] (O)O[C@H] (CO)[C@@H] (O[C@@H]2O[C@H] (CO)[C@@H] (O)[C@H] (O)[C@H]2N)[C@@H]1O. 1S/C12H24N2O9/c13-5-9 (19)10 (4 (2-16)21-11 (5)20)23-12-6 (14)8 (18)7 (17)3 (1-15)22-12/h3-12, 15-20H, 1-2, 13-14H2/t3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12+/m1/s1. QLTSDROPCWIKKY-PMCTYKHCSA-N. | |
| cycloisomaltooligosaccharide glucanotransferase | Specific for (1?6)-α-D-glucans (dextrans) and, unlike cyclomaltodextrin glucanotransferase (EC 2.4.1.19), without activity towards (1?4)-α-D-glucans, such as amylose. It also has no activity on oligosaccharides, such as amylopectin and pullulan,containing (1?6)-α-D-glucosidic linkages at branch points. The enzyme from Bacillus circulans T-3040 has been shown to form cycloisomalto-oligosaccharides of three sizes (7, 8 and 9 glucose units). It will also catalyse the disproportionation of two isomalto-oligosaccharides molecules to yield a series of isomalto-oligosachharides and the addition of D-glucose to cycloisomalto-oligosaccharides with ring opening to form isomalto-oligosaccharides. Group: Enzymes. Enzyme Commission Number: EC 2.4.1.248. 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-2477; cycloisomaltooligosaccharide glucanotransferase; EC 2.4.1.248. Cat No: EXWM-2477. | |
| D-Cello-oligosaccharides | | |
| D-Fructose oligosaccharides (DP2-8) | | |
| dolichyl-diphosphooligosaccharide-protein glycotransferase | Occurs in eukaryotes that form a glycoprotein by the transfer of a glucosyl-mannosyl-glucosamine polysaccharide to the side-chain of an L-asparagine residue in the sequence -Asn-Xaa-Ser- or -Asn-Xaa-Thr- (Xaa not Pro) in nascent polypeptide chains. The basic oligosaccharide is the tetradecasaccharide Glc3Man9GlcNAc2 (for diagram click here). However, smaller oligosaccharides derived from it and oligosaccharides with additional monosaccharide units attached may be involved. See ref for a review of N-glycoproteins in eukaryotes. Man3GlcNAc2 seems to be common for all of the oligosaccharides involved with the terminal N-acetylglucosamine linked to the protein L-aspa... oligopolysaccharidotransferase; STT3. Enzyme Commission Number: EC 2.4.99.18. CAS No. 75302-32-8. 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-2702; dolichyl-diphosphooligosaccharide-protein glycotransferase; EC 2.4.99.18; 75302-32-8; dolichyldiphosphooligosaccharide-protein glycosyltransferase; asparagine N-glycosyltransferase; dolichyldiphosphooligosaccharide-protein oligosaccharyltransferase; dolichyl pyrophosphodiacetyl chitobiose-protein glycosyltransferase; oligomannosyltransferase; oligosaccharide transferase; dolichyldiphosphoryloligosaccharide-protein oligosaccharyl | |
| Fructo-oligosaccharide DP10/GF9 | Fructo-oligosaccharide DP10/GF9 is a fructooligosaccharides isolated from many plants such as sugarcane. Grades: 0.98. CAS No. 118150-64-4. Molecular formula: C60H102O51. Mole weight: 1639.4. | |
| Fucosyl GM1 oligosaccharide | Fucosyl GM1 oligosaccharide is a multifaceted biomedical compound with immune response augmentation and neuroprotective potency. Fucosyl GM1 oligosaccharide has applications in research of Alzheimer's disease, Parkinson's disease and multiple sclerosis. Synonyms: Fuca1-2Galb1-3GalNAcb1-4(Neu5Aca2-3)Galb1-4Glc. Molecular formula: C43H71N2O33Na. Mole weight: 1167.01. | |
| Galacturonan oligosaccharides DP range : 25-50 sodium salt | | |
| GD1a-Oligosaccharide | GD1a-Oligosaccharide is an esteemed compound, demonstrating remarkable potential in studying peripheral neuropathies as well as neurodegenerative disorders. Functioning as an astute modulator of ganglioside metabolism, it exerts an exquisite influence on nerve cell viability while stimulating the process of neuronal regeneration. Synonyms: GD1aSaccharide. CAS No. 1627679-86-0. Molecular formula: C48H79N3O37. Mole weight: 1290.14. | |
| GD1b-Oligosaccharide | GD1b-Oligosaccharide is a crucial component widely used in the research of neurological diseases, including Alzheimer's and Parkinson's. With its bioactive properties, GD1b-Oligosaccharide holds promise for targeted drug delivery systems, disease diagnostics and advanced research in neurobiology. Synonyms: Galb1-3GalNAcb1-4(Neu5Aca2-8Neu5Aca2-3)Galb1-4Glc. Molecular formula: C48H77N3O37Na2. Mole weight: 1334.10. | |
| GD2-Oligosaccharide | GD2-Oligosaccharide is a biomedical product used in the research of neuroblastoma. It has been found to target the GD2 antigen present on neuroblastoma cells. Molecular formula: C42H67N3O32Na2. Mole weight: 1171.96. | |
| GD2-Oligosaccharide-b-(N-acetyl-propargyl) | GD2-Oligosaccharide-b-(N-acetyl-propargyl) is a remarkable biomedical compound, emerging as a formidable compound in the research of neuroblastoma, an affliction predominantly encountered during early stages of life. Synonyms: GD2-Saccharide-b-NAc-propargyl. Molecular formula: C47H72N4O32Na2. Mole weight: 1251.06. | |
| GD2-Oligosaccharide-desthiobiotin | GD2-Oligosaccharide-desthiobiotin is a compound product used in the research of GD2-positive cancers, composed of desthiobiotin and GD2 oligosaccharide. It specifically targets GD2 receptors on cancer cells. Molecular formula: C65H106N10O37 2Na. Mole weight: 1665.56. | |
| GD2-Oligosaccharide-sp-biotin | GD2-Oligosaccharide-sp-biotin is a powerful tool used for researching various diseases such as neuroblastoma, melanoma and certain other cancers. It specifically targets GD2 oligosaccharide. The addition of biotin enables efficient detection and purification of GD2 oligosaccharide in experimental settings. Molecular formula: C65H104N10O37SNa2. Mole weight: 1695.61. | |
| Glucomannan oligosaccharides | | |
| Glycosaminoglycan related oligosaccharides | | |
| Glycyl-Oligosaccharidesmannose 1 | Glycyl-Oligosaccharidesmannose 1 is an intriguing and cutting-edge biomedical resource, assuming an indispensable function by studying manifold maladies attributed to a scarcity of mannose. Molecular formula: C24H42N4O16. Mole weight: 642.61. | |
| Glycyl-Oligosaccharidesmannose 3(a) | Glycyl-Oligosaccharidesmannose 3(a) is a quintessential compound, unveiling its prowess in studying glycosylation disorders. Molecular formula: C36H62N4O26. Mole weight: 966.89. | |
| Glycyl-Oligosaccharidesmannose 5 | Glycyl-Oligosaccharidesmannose 5 is a crucial compound utilized in the biomedical industry to study beta-mannosidosis. This product aids in the breakdown of complex sugars, promoting enzyme activity and preventing the accumulation of harmful substances. It plays a vital role in studying symptoms associated with this rare genetic disorder. Molecular formula: C48H82N4O36. Mole weight: 1291.17. | |
| Glycyl-Oligosaccharidesmannose 6 | Glycyl-Oligosaccharidesmannose 6 is a biomedical compound serving for studying lysosomal storage disorders, most notably Mannosidosis. Functioning as a highly crucial substrate for the powerful enzyme β-mannosidase, it exerts a significant influence on the degradation process of surplus oligosaccharides. Molecular formula: C54H92N4O41. Mole weight: 1453.31. | |
| GM1a-Oligosaccharide | GM1a-Oligosaccharide is a cutting-edge compound designated for research in neurodegenerative maladies, namely the formidable Parkinson's disease and Alzheimer's disease. Its pronounced efficacy stems from its remarkable capacity to augment the physiological process of neuronal regeneration while concurrently proactively mitigating neuronal cell mortality. Synonyms: Galb1-3GalNAcb1-4(Neu5Aca2-3)Galb1-4Glc. Molecular formula: C37H61N2O29Na. Mole weight: 1020.87. | |
| GM1b-Oligosaccharide | GM1b-Oligosaccharide is an innovative and promising compound, showcasing its potential in studying complex neurodegenerative ailments including Parkinson's and Alzheimer's diseases. Derived from the GM1 ganglioside, this compound offers a remarkable neuroprotective effect by significantly augmenting neuronal survival and effectively thwarting cognitive decline. Molecular formula: C37H61N2O29Na. Mole weight: 1020.87. | |
| GM2-Oligosaccharide | GM2-Oligosaccharide is a prominent constituent in the realm of biomedical applications, finding extensive utility in the investigation of lysosomal storage disorders. Acting as an invaluable compoundin the scientific domain, this oligosaccharide facilitates the exploration of intricate processes underlying GM2 ganglioside metabolism. Molecular formula: C31H51N2O24Na. Mole weight: 858.73. | |
| GM2-Oligosaccharide-spacer-NH2 ammonium | GM2-Oligosaccharide-spacer-NH2 ammonium is a vital compound used in biomedicine. Its application lies in the treatment of GM2 gangliosidoses, a group of genetic disorders caused by the deficiency of vital enzymes. Synonyms: GalNAcb-4(NeuAca2-3)Galb-4Glcb-NAc-spacer-NH2. Molecular formula: C44H75N7O27·NH3. Mole weight: 1151.13. | |
| GM2-Oligosaccharide-sp-biotin | | |
| GQ3-Oligosaccharide | GQ3-Oligosaccharide is an extraordinary bioactive compound employed in the research of neurodegenerative ailments, showcasing remarkable neuroprotective attributes. GQ3-Oligosaccharide actively contributes to the diminution of oxidative stress and inflammation, thereby facilitating the augmentation of neuronal viability and efficacious functioning. Synonyms: Neu5Aca2-8Neu5Aca2-8Neu5Acb2-8Neu5Aca2-3Galb1-4Glc. Molecular formula: C56H86N4O43Na4. Mole weight: 1595.24. | |
| GT1a-Oligosaccharide | GT1a-Oligosaccharide is an advanced oligosaccharide, finding applications in studying intricate neurological afflictions. Its specialized affinity towards toxins and pathogens endows it with unparalleled efficiency in studying viral invasions. Synonyms: Neu5Aca2-8Neu5Aca2-3Galb1-3GalNAcb1-4 (Neu5Aca2-3)Galb1-4Glc. Molecular formula: C59H93N4O45Na3. Mole weight: 1647.34. | |
| GT1b-Oligosaccharide | GT1b-Oligosaccharide is an extraordinary compound, manifesting promising applications in studying the complexities of neurological disorders and autoimmune diseases. CAS No. 75663-36-4. Molecular formula: C59H96N4O45. Mole weight: 1581.39. | |
| GT1c-Oligosaccharide | GT1c-Oligosaccharide is a remarkable compound widely utilized in studying intricate cellular mechanisms in a spectrum of ailments, such as debilitating cancers and complex neurodegenerative disorders. Synonyms: Galb1-3GalNAcb1-4(Neu5Aca2-8Neu5Aca2-8Neu5Aca2-3)Galb1-4Glc. Molecular formula: C59H93N4O45Na3. Mole weight: 1647.34. | |
| GT2-Oligosaccharide | GT2-Oligosaccharide is a multifaceted biomedical marvel, effectively aiding in the formidable research of cardiovascular diseases, cancer, and diabetes. Acting as a prowess-inducing inhibitor of α-glucosidases, this spellbinding remedy boasts unprecedented potential in orchestrating the delicate symphony of blood glucose regulation. Synonyms: GalNAcb1-4(Neu5Aca2-8Neu5Aca2-8Neu5Aca2-3)Galb1-4Glc. Molecular formula: C53H83N4O40Na3. Mole weight: 1485.20. | |
| GT3-Oligosaccharide | GT3-Oligosaccharide is an extraordinary biomedical compound emanating from pristine natural sources, acting as a potent antioxidant. It is anti-inflammatory and immunomodulatory crusader, finding applications in studying cancer, cardiovascular ailments and neurodegenerative ravages. Synonyms: Neu5Aca2-8Neu5Aca2-8Neu5Aca2-3Galb1-4Glc. Molecular formula: C45H70N3O35Na3. Mole weight: 1282.01. | |
| Heparin sulfate NS-oligosaccharide NS | | |
| Heparin sulfate oligosaccharide NAc | | |
| high-mannose-oligosaccharide β-1,4-N-acetylglucosaminyltransferase | The activity of the intersecting mannose residue as acceptor is dependent on two other mannose residues attached by α-1,3 and α-1,6 links. Group: Enzymes. Synonyms: uridine diphosphoacetylglucosamine-oligosaccharide acetylglucosaminyltransferase; acetylglucosamine-oligosaccharide acetylglucosaminyltransferase; UDP-GlcNAc:oligosaccharide β-N-acetylglucosaminyltransferase; UDP-N-acetyl-D-glucosamine:high-mannose-oligosaccharide β-1,4-N-acetylglucosaminyltransferase. Enzyme Commission Number: EC 2.4.1.197. CAS No. 123425-54-7. 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-2424; high-mannose-oligosaccharide β-1,4-N-acetylglucosaminyltransferase; EC 2.4.1.197; 123425-54-7; uridine diphosphoacetylglucosamine-oligosaccharide acetylglucosaminyltransferase; acetylglucosamine-oligosaccharide acetylglucosaminyltransferase; UDP-GlcNAc:oligosaccharide β-N-acetylglucosaminyltransferase; UDP-N-acetyl-D-glucosamine:high-mannose-oligosaccharide β-1,4-N-acetylglucosaminyltransferase. Cat No: EXWM-2424. | |
| Maltodextrin oligosaccharides - DP10 to DP40 | | |
| Maltodextrin oligosaccharides - DP2 to DP15 | | |
| Maltose alternan oligosaccharide | Maltose alternan oligosaccharide is a biomedical product used to study various health condition such as diabetes. Additionally, research suggests that it may have antioxidant and anti-inflammatory properties, making it useful in studying oxidative stress-related diseases. Synonyms: MAOS. | |
| mannosyl-oligosaccharide 1,2-α-mannosidase | Involved in the synthesis of glycoproteins. Group: Enzymes. Synonyms: mannosidase 1A; mannosidase 1B; 1,2-α-mannosidase; exo-α-1,2-mannanase; mannose-9 processing α-mannosidase; glycoprotein processing mannosidase I; mannosidase I; Man9-mannosidase; ManI; 1,2-α-mannosyl-oligosaccharide α-D-mannohydrolase. Enzyme Commission Number: EC 3.2.1.113. CAS No. 9068-25-1. 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-3796; mannosyl-oligosaccharide 1,2-α-mannosidase; EC 3.2.1.113; 9068-25-1; mannosidase 1A; mannosidase 1B; 1,2-α-mannosidase; exo-α-1,2-mannanase; mannose-9 processing α-mannosidase; glycoprotein processing mannosidase I; mannosidase I; Man9-mannosidase; ManI; 1,2-α-mannosyl-oligosaccharide α-D-mannohydrolase. Cat No: EXWM-3796. | |
| mannosyl-oligosaccharide 1,3-1,6-α-mannosidase | Involved in the synthesis of glycoproteins. Group: Enzymes. Synonyms: mannosidase II; exo-1,3-1,6-α-mannosidase; α-D-mannosidase II; α-mannosidase II; α1-3,6-mannosidase; GlcNAc transferase I-dependent α1,3[α1,6]mannosidase; Golgi α-mannosidase II; ManII; 1,3(1,6)-α-D-mannosidase; 1,3-(1,6-)mannosyl-oligosaccharide α-D-mannohydrolase. Enzyme Commission Number: EC 3.2.1.114. CAS No. 82047-77-6. 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-3797; mannosyl-oligosaccharide 1,3-1,6-α-mannosidase; EC 3.2.1.114; 82047-77-6; mannosidase II; exo-1,3-1,6-α-mannosidase; α-D-mannosidase II; α-mannosidase II; α1-3,6-mannosidase; GlcNAc transferase I-dependent α1,3[α1,6]mannosidase; Golgi α-mannosidase II; ManII; 1,3(1,6)-α-D-mannosidase; 1,3-(1,6-)mannosyl-oligosaccharide α-D-mannohydrolase. Cat No: EXWM-3797. | |
| mannosyl-oligosaccharide glucosidase | Also acts, more slowly, on the corresponding glycolipids and glycopeptides. Involved in the formation of high-mannose and complex glycoproteins. Group: Enzymes. Synonyms: Glc3Man9NAc2 oligosaccharide glucosidase; trimming glucosidase I. Enzyme Commission Number: EC 3.2.1.106. CAS No. 78413-07-7. 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-3789; mannosyl-oligosaccharide glucosidase; EC 3.2.1.106; 78413-07-7; Glc3Man9NAc2 oligosaccharide glucosidase; trimming glucosidase I. Cat No: EXWM-3789. | |
| membrane-oligosaccharide glycerophosphotransferase | β-Linked glucose residues in simple glucosides, such as gentiobiose, can act as acceptors. In the presence of low concentrations of acceptor, free cyclic 1,2-phosphoglycerol is formed. Group: Enzymes. Synonyms: periplasmic phosphoglycerotransferase; phosphoglycerol cyclase. Enzyme Commission Number: EC 2.7.8.21. CAS No. 80146-86-7. 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-3321; membrane-oligosaccharide glycerophosphotransferase; EC 2.7.8.21; 80146-86-7; periplasmic phosphoglycerotransferase; phosphoglycerol cyclase. Cat No: EXWM-3321. | |
| Neoagaro oligosaccharides | | |
| phosphatidylglycerol-membrane-oligosaccharide glycerophosphotransferase | 1,2-β- and 1,6-β-linked glucose residues in membrane polysaccharides and in synthetic glucosides can act as acceptors. Group: Enzymes. Synonyms: phosphoglycerol transferase; oligosaccharide glycerophosphotransferase; phosphoglycerol transferase I. Enzyme Commission Number: EC 2.7.8.20. CAS No. 80146-86-7. 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-3320; phosphatidylglycerol-membrane-oligosaccharide glycerophosphotransferase; EC 2.7.8.20; 80146-86-7; phosphoglycerol transferase; oligosaccharide glycerophosphotransferase; phosphoglycerol transferase I. Cat No: EXWM-3320. | |
| undecaprenyl-diphosphooligosaccharide-protein glycotransferase | A bacterial enzyme that has been isolated from Campylobacter jejuni and Campylobacter lari. It forms a glycoprotein by the transfer of a glucosyl-N-acetylgalactosaminyl-N,N'-diacetylbacillosamine (GalNAc2(Glc)GalNAc3diNAcBac) polysaccharide and related oligosaccharides to the side-chain of an L-asparagine residue in the sequence -Asp/Glu-Xaa-Asn-Xaa'-Ser/Thr- (Xaa and Xaa' not Pro) in nascent polypeptide chains. Requires Mn2+ or Mg2+. Occurs on the external face of the plasma membrane. The polyprenol involved is normally tritrans,heptacis-undecaprenol but a decaprenol is used by some species. Group: Enzymes. Synonyms: PglB. Enzyme Commission Number: EC 2.4.99.19. 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-2703; undecaprenyl-diphosphooligosaccharide-protein glycotransferase; EC 2.4.99.19; PglB. Cat No: EXWM-2703. | |
| Xyloglucan oligosaccharides - from tamarind seed | | |
| 1,2,3,4,6-Penta-O-acetyl-1-thio-β-D-galactopyranose | 1-Thio-β-D-galactopyranose, acetylated at positions 2,3,4,5,6, is an intricate chemical compound that serves as a distinguished reactant for the production of complex oligosaccharides. Its diverse applications include the creation of high-capacity β-galactosidase inhibitors for plausible therapies of lactose intolerance and varying scientific experiments. The compound's adeptness to acetylate five positions of β-D-galactopyranose molecule, and form disaccharide linkages with various other sugars, makes it a critical reagent in achieving structural diversity and examining the structure-activity relationship of saccharides. Synonyms: 1,2,3,4,6-Penta-O-acetyl-1-thio-beta-D-galactopyranose; NSC89877; Glucopyranose deriv.; Oprea1_802175; DTXSID70929370; NSC-89877; NSC409737; AKOS005591985; NSC-409737; FT-0674883.alpha.-D-Glucopyranose, 1-thio-, pentaacetate; 2,3,4,6-Tetra-O-acetyl-1-S-acetyl-1-thio-.alpha.-D-glucopyranose; (3,4,5-triacetoxy-6-acetylsulfanyl-tetrahydropyran-2-yl)methyl acetate; 3,5-BIS(ACETYLOXY)-2-[(ACETYLOXY)METHYL]-6-(ACETYLSULFANYL)TETRAHYDRO-2H-PYRAN-4-YL ACETATE. CAS No. 6806-56-0. Molecular formula: C16H22O10S. Mole weight: 406.4. | |
| 1,2,3,4,6-Penta-O-acetyl-a-D-galactopyranose | Complex oligosaccharides and glycoconjugates in biomedicine require a quintessential intermediate to synthesize efficientlybehold, 1,2,3,4,6-Penta-O-acetyl-a-D-galactopyranose. This key compound serves as the cornerstone of building blocks for an assortment of drugs, including those aimed at combating cancer and boosting immunotherapy efficacy. Synonyms: a-D-Galactose pentaacetate. CAS No. 4163-59-1. Molecular formula: C16H22O11. Mole weight: 390.34. | |
| 1-(2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl)imidazole | 1-(2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl)imidazole, a highly efficient glycosylation reagent, has shown remarkable utility in the synthesis of glycans and glycoconjugates. Its applications have expanded to the development of glycoside hydrolase inhibitors as well as in the preparation of oligosaccharides. The versatility and efficacy of this chemical compound make it a valuable tool in glycosylation research. Synonyms: 1-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)imidazole; 38953-70-7; [(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-imidazol-1-yloxan-2-yl]methyl acetate; DTXSID60855871; 1-(2,3,4,6-Tetra-O-acetyl-beta-D-glucopyranosyl)-1H-imidazole; [(2R,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-(1H-imidazol-1-yl)oxan-2-yl]methyl acetate; (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(1H-imidazol-1-yl)tetrahydro-2H-pyran-3,4,5-triyl triacetate. CAS No. 38953-70-7. Molecular formula: C17H22N2O9. Mole weight: 398.4. | |
| 1,2,3,4-Tetra-O-acetyl-6-O-(tert-butyldiphenylsilyl)-b-D-glucopyranose | 1,2,3,4-Tetra-O-acetyl-6-O-(tert-butyldiphenylsilyl)-b-D-glucopyranose, a crucial intermediate of carbohydrates, has multiplicative significance in the synthesis of glycosylated natural products and pharmaceuticals. In oligosaccharide and glycopeptide synthesis, it prevails ubiquitously and serves as a consistent starting material. This synthetic intermediate has apparent potential as a precursor for creating glycosidase inhibitors, which act as vital pharmaceutical agents. Molecular formula: C30H38O10Si. Mole weight: 586.72. | |
| 1,2,3,4-Tetra-O-acetyl-6-O-triisopropylsilyl-a-D-mannopyranose | 1,2,3,4-Tetra-O-acetyl-6-O-triisopropylsilyl-a-D-mannopyranose is a carbohydrate derivative that serves as a crucial intermediate in the chemical synthesis of diverse glycosylated compounds. This molecule is often employed in the preparation of both glycosyl donors and acceptors, which then go on to form a host of chemically diverse oligosaccharides possessing a range of biological activities. Among its many applications, 1,2,3,4-Tetra-O-acetyl-6-O-triisopropylsilyl-a-D-mannopyranose is invaluable for the synthesis of a variety of biologically active glycosylated natural products, glycoproteins, and carbohydrate-based vaccines. Molecular formula: C23H40O10Si. Mole weight: 504.66. | |
| 1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldimethylsilyl-b-D-galactopyranose | 1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldimethylsilyl-b-D-galactopyranose, a noteworthy chemical compound, has garnered attention in the realm of oncology for its potential in the development of pioneering drugs to battle prevalent illnesses such as breast and lung cancer. Additionally, it has shown its versatility as a reagent in carbohydrate chemistry, and as a fundamental building block in the synthesis of intricate oligosaccharides. Its significance cannot be underestimated in these domains, providing a crucial foundation for cutting-edge research and breakthrough discoveries. Molecular formula: C40H42O10Si. Mole weight: 710.86. | |
| 1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldimethylsilyl-b-D-glucopyranose | 1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldimethylsilyl-b-D-glucopyranose, a derivative of carbohydrates, serves as a fundamental component in the syntheses of glycopeptides, glycoproteins, and glycolipids. This carbohydrate derivative further showcases its significance in the production of oligosaccharide antigens. Molecular formula: C40H42O10Si. Mole weight: 710.86. | |
| 1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldiphenylsilyl-a-D-mannopyranose | 1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldiphenylsilyl-a-D-mannopyranose, a derivative of carbohydrate, is widely employed in the production of glycosylated natural products and oligosaccharides. Its utility as a primary component in the synthesis of diverse glycosylated drugs, inclusive of antiviral drugs and anticancer agents, is notable. Molecular formula: C40H42O10Si. Mole weight: 710.86. | |
| 1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldiphenylsilyl-b-D-galactopyranose | 1,2,3,4-Tetra-O-benzoyl-6-O-tert-butyldiphenylsilyl-b-D-galactopyranose is a paramount chemical reagent employed in oligosaccharides' synthesis, extensively adopted in biomedical research to investigate carbohydrates' significance in biological systems, and design advanced therapies and therapeutics for previously untreatable diseases countenancing cancer and infectious diseases - its impact and admissibility towards this domain remains prodigious and prodigiously relevant. Molecular formula: C40H42O10Si. Mole weight: 710.86. | |
| 1,2,3,4-Tetra-O-benzoyl-6-O-triisopropylsilyl-b-D-galactopyranose | 1,2,3,4-Tetra-O-benzoyl-6-O-triisopropylsilyl-b-D-galactopyranose, a vital synthetic intermediate, exhibits crucial applications in the production of numerous glycopeptides and glycolipids. Studies suggest that the compound serves as a valuable donor in the one-pot synthesis of ganglioside GM1 hexasaccharide. Moreover, its utilization in the preparation of oligosaccharides found in breast cancer antigens emphasizes its significance. The complex nature of the compound, with its high degree of perplexity and burstiness, renders it an essential ingredient in the field of bio-organic chemistry. Molecular formula: C46H54O10Si. Mole weight: 795.02. | |
| 1,2,3,4-Tetra-O-benzoyl-a-D-glucuronide methyl ester | 1,2,3,4-Tetra-O-benzoyl-α-D-glucuronide methyl ester, a compound of considerable interest in glycoside synthesis, is specifically useful in producing oligosaccharides that contain β-galactopyranosyl or N-acetyllactosamine units. It has an additional utility as a protective group for glucuronide derivatives in carbohydrate chemistry. By serving as a reagent, it allows for efficient amination of carbohydrates. Its employment is characterized by a high degree of perplexity due to the intricacy of the chemical processes, along with a pronounced degree of burstiness due to the variation in lengths of the respective oligosaccharides. Molecular formula: C35H28O11. Mole weight: 624.59. | |
| 1,2,3,4-Tetra-O-pivaloyl-6-O-(tert-butyldimethylsilyl)-b-D-glucopyranose | 1,2,3,4-Tetra-O-pivaloyl-6-O-(tert-butyldimethylsilyl)-b-D-glucopyranose is a highly significant and pivotal chemical compound extensively utilized in the synthesis of a multitude of therapeutic drugs for tackling the ailments of diabetes and cancer. Its fundamental application lies in the generation of glycosyl donors essential for oligosaccharide synthesis and as a crucial reagent employed in glycosylation reactions. The multifaceted role of this compound in medicinal chemistry makes it an indispensable asset for pharmaceutical research and development. Molecular formula: C32H58O10Si. Mole weight: 630.90. | |
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