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| Product | Description | |
|---|---|---|
| 1,2:3,4-Di-O-isopropylidene-a-L-galactopyranose | 1,2:3,4-Di-O-isopropylidene-a-L-galactopyranose, a chemical entity well-known for its ability to shield reactive hydroxyls, plays a fundamental role in the domain of carbohydrate and glycolipid synthesis. Its instrumental pertinence in rational drug design and disease-related investigations lies in the identification and characterization of key carbohydrate-mediated biomolecules. By enabling versatile derivatization of galactose's hallowed hydroxyls, this compound facilitates manifold research avenues. Synonyms: alpha-L-Galactopyranose, 1,2:3,4-bis-O-(1-methylethylidene)-; 1-O,2-O:3-O,4-O-Diisopropylidene alpha-L-galactopyranose; ((3AS,5S,5aR,8aR,8bS)-2,2,7,7-tetramethyltetrahydro-5H-bis([1,3]dioxolo)[4,5-b:4',5'-d]pyran-5-yl)methanol. Grade: ≥95%. CAS No. 70932-37-5. Molecular formula: C12H20O6. Mole weight: 260.28. |  |
| 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 shows its significance in the production of oligosaccharide antigens. 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-benzyl-6-O-tert-butyldimethylsilyl-a-D-mannopyranose | 1,2,3,4-Tetra-O-benzyl-6-O-tert-butyldimethylsilyl-a-D-mannopyranose, a crucial compound in carbohydrate chemistry, exhibits multifarious utility in the production of glycosyl donors and acceptors. Its employment extends to the synthesis of glycoproteins and glycolipids as well. The manifold abilities of this compound make it an indispensable tool for researchers in the field of glycoscience. Molecular formula: C40H50O6Si. Mole weight: 654.93. | |
| 1,2,3,4-Tetra-O-benzyl-a-D-mannopyranoside | 1,2,3,4-Tetra-O-benzyl-α-D-mannopyranoside, an exceptionally powerful biomedicine compound, stands as a paramount therapeutic agent addressing a myriad of afflictions. By impeding glycosylation, this potent marvel assumes a pivotal function in the synthesis of glycoproteins and glycolipids. Embracing a vast potential, it showcases promising applications in the realms of anti-cancer therapy, immunology, and microbial exploration. Synonyms: Benzyl 2,3,4-tri-O-benzyl-a-D-mannopyranoside. CAS No. 57783-76-3. Molecular formula: C34H36O6. Mole weight: 540.65. | |
| 1,2,3,6-Tetra-O-benzoyl-b-D-mannopyranose | 1,2,3,6-Tetra-O-benzoyl-b-D-mannopyranose is a carbohydrate moiety harnessed for glycoconjugate biosynthesis - molecules bearing carbohydrates linked covalently to proteins or lipids. Frequently utilized for the synthesis of glycopeptides and glycolipids, these play pivotal roles in the exploration of infectious ailments and neoplasms. The molecule's intricate structure confers a lasting impact on the formation and investigation of biologically relevant chemical compounds. CAS No. 171482-60-3. Molecular formula: C34H28O10. Mole weight: 596.58. | |
| 1,2,4,6-Tetra-O-acetyl-3-azido-3-deoxy-D-glucopyranose | 1,2,4,6-Tetra-O-acetyl-3-azido-3-deoxy-D-glucopyranose, a highly versatile azido sugar, finds wide application in the synthesis of glycoconjugates, including glycolipids, glycopeptides, and oligosaccharides. Its capacity to engage with alkynes through click chemistry makes it a potent investigative tool for studying glycosylation and also holds considerable promise in the treatment of diverse inflammatory and autoimmune disorders. Consequently, this compound promises to be indispensable to a range of cutting-edge scientific endeavors. CAS No. 185114-94-7. Molecular formula: C14H19N3O9. Mole weight: 373.32. | |
| 1,2-diacylglycerol 3-α-glucosyltransferase | The enzyme from the bacterium Acholeplasma laidlawii, which lacks a cell wall, produces the major non-bilayer lipid in the organism. The enzyme from the bacterium Agrobacterium tumefaciens acts under phosphate deprivation, generating glycolipids as surrogates for phospholipids. The enzyme belongs to the GT4 family of configuration-retaining glycosyltransferases. Many diacylglycerols with long-chain acyl groups can act as acceptors. cf. EC 2.4.1.336, monoglucosyldiacylglycerol synthase. Group: Enzymes. Synonyms: mgs (gene name); UDP-glucose:diacylglycerol glucosyltransferase; UDP-glucose:1,2-diacylglycerol glucosyltransferase; uridine diphosphoglucose-diacylglycerol glucosyltransferas. Enzyme Commission Number: EC 2.4.1.337. 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-2575; 1,2-diacylglycerol 3-α-glucosyltransferase; EC 2.4.1.337; mgs (gene name); UDP-glucose:diacylglycerol glucosyltransferase; UDP-glucose:1,2-diacylglycerol glucosyltransferase; uridine diphosphoglucose-diacylglycerol glucosyltransferase; UDP-glucose-diacylglycerol glucosyltransferase; UDP-glucose:1,2-diacylglycerol 3-D-glucosyltransferase; UDP-glucose:1,2-diacyl-sn-glycerol 3-D-glucosyltransferase; 1,2-diacylglycerol 3-glucosyltransferase (ambiguous). Cat No: EXWM-2575. |  |
| 1,2-Dipalmitoyl-3-iododeoxy-rac-glycerol | 1,2-Dipalmitoyl-3-iododeoxy-rac-glycerol is used to prepare glycolipid amphipathic micellar delivery systems for DNA and RNA biological active polyions. Group: Biochemicals. Grades: Highly Purified. CAS No. 40290-36-6. Pack Sizes: 10mg, 25mg. Molecular Formula: C35H67IO4, Molecular Weight: 678.81. US Biological Life Sciences. |  Worldwide |
| 1,2-Dipalmitoyl-3-iododeoxy-rac-glycerol-d5 | 1,2-Dipalmitoyl-3-iododeoxy-rac-glycerol-d5 is labelled 1,2-Dipalmitoyl-3-iododeoxy-rac-glycerol (D486925) which is used to prepare glycolipid amphipathic micellar delivery systems for DNA and RNA biological active polyions. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C35H62D5IO4, Molecular Weight: 683.84. US Biological Life Sciences. | Worldwide |
| 1,3,6-Tri-O-benzoyl-2-deoxy-a-D-glucopyranoside | 1,3,6-Tri-O-benzoyl-2-deoxy-a-D-glucopyranoside - a primary chemical in glycobiology research - functions as a noteworthy molecular probe to identify lectins or carbohydrate-binding proteins. Additionally, it has revealed its potential in synthesizing glycosyl derivatives, mimetics of polysaccharides, and glycolipids for scientific and academic purposes. Molecular formula: C27H30O5. Mole weight: 434.52. | |
| 1,3-Di-O-acetyl-2-deoxy-5-O-benzoyl-L-erythro-pentofuranose | 1,3-Di-O-acetyl-2-deoxy-5-O-benzoyl-L-erythro-pentofuranose is a complex, synthetic compound that finds wide-ranging applications in the field of biochemistry and carbohydrate chemistry. It serves as an essential building block for a diverse array of glycoproteins and glycolipids, owing to its unique chemical properties and structural features. Moreover, its crucial role in numerous research projects underscores the significant contribution this compound continues to make towards advancing our understanding of complex biological systems. Molecular formula: C16H18O7. Mole weight: 322.31. | |
| 13-hydroxydocosanoate 13-β-glucosyltransferase | 13-β-D-Glucosyloxydocosanoate can also act as acceptor, leading to the formation by Candida bogoriensis of the extracellular glycolipid, hydroxydocosanoate sophoroside diacetate. Group: Enzymes. Synonyms: 13-glucosyloxydocosanoate 2'-β-glucosyltransferase; UDP-glucose:13-hydroxydocosanoic acid glucosyltransferase; uridine diphosphoglucose-hydroxydocosanoate glucosyltransferase; UDP-glucose-13-hydroxydocosanoate glucosyltransferase. Enzyme Commission Number: EC 2.4.1.158. CAS No. 70457-13-5. 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-2382; 13-hydroxydocosanoate 13-β-glucosyltransferase; EC 2.4.1.158; 70457-13-5; 13-glucosyloxydocosanoate 2'-β-glucosyltransferase; UDP-glucose:13-hydroxydocosanoic acid glucosyltransferase; uridine diphosphoglucose-hydroxydocosanoate glucosyltransferase; UDP-glucose-13-hydroxydocosanoate glucosyltransferase. Cat No: EXWM-2382. | |
| 18:0(2S-OH) Sulfo GalCer Ammonium salt | 18:0(2S-OH) Sulfo GalCer Ammonium salt, a synthetic compound employed in biomedical research, has the capacity to serve as a potent therapeutic agent for the treatment of various malignancies- specifically leukemia and lymphoma. Boasting versatile therapeutic potential, it has been shown to exhibit anti-inflammatory properties, and has exciting potential for the treatment of autoimmune diseases like multiple sclerosis. With its staggering attributes as a sulfo glycolipid, this intriguing compound holds tremendous promise and warrants thorough exploration in the realm of drug development. Synonyms: 3-O-sulfo-D-galactosyl-β-1,1'-N-[2''(S)-hydroxystearoyl]-D-erythro-sphingosine (ammonium salt); Ammonium (2S,3R,4E)-3-hydroxy-2-{[(2S)-2-hydroxyoctadecanoyl]amino}-4-octadecen-1-yl 3-O-sulfonato-β-D-threo-hexopyranoside; Octadecanamide, 2-hydroxy-N-[(1S,2R,3E)-2-hydroxy-1-[[(3-O-sulfo-β-D-galactopyranosyl)oxy]methyl]-3-heptadecen-1-yl]-, ammonium salt (1:1), (2S)-. Grade: >99%. CAS No. 2260670-28-6. Molecular formula: C42H84N2O12S. Mole weight: 841.19. | |
| 1-D-a-Galactopyranosyl-4-O-[1-(2-octadecylthioethyl)-(b-D-galactopyranoside)] | 1-D-a-Galactopyranosyl-4-O-[1-(2-octadecylthioethyl)-(b-D-galactopyranoside)] is a synthetic glycolipid. In immunology, it plays a vital role as an immune system stimulator, aiding in the development and research of vaccines and therapeutics for infectious diseases. | |
| 1H,1H,2H,2H-Perfluorooctyl-1-thiol | 1H,1H,2H,2H-Perfluorooctyl-1-thiol acts as a reagent in the preparation, structure, and antitumor activity of dinuclear arene ruthenium thiolato complexes with fluorous side-chains. Reagent in the preparation of glycolipidic nitrones as potential antioxidant drugs for neurodegenerative disorders. Group: Biochemicals. Grades: Highly Purified. CAS No. 34451-26-8. Pack Sizes: 500mg, 1g. Molecular Formula: C8H5F13S. US Biological Life Sciences. | Worldwide |
| 2-[2-[2- (2-Chloroethoxy) ethoxy]ethoxy]ethanol | 2-[2-[2- (2-Chloroethoxy) ethoxy]ethoxy]ethanol is a polyethylene glycol used in the synthesis of novel glycolipids that bind HIV-1 cell surface glycoprotein Gp120 with potential application to pharmaceutical HIV-1 drugs. Also used in the synthesis of PET imaging agents targeting brain β-amyloid. Group: Biochemicals. Alternative Names: 11-Chloro-3,6,9-trioxa-1-undecanol; 11-Chloro-3,6,9-trioxaundecanol; 2- (2- (2- (2-Chloroethoxy) ethoxy) ethoxyethanol; Triethylene Glycol Mono(2-chloroethyl)ether. Grades: Highly Purified. CAS No. 5197-66-0. Pack Sizes: 250mg. Molecular Formula: C?H??ClO?, Molecular Weight: 212.67. US Biological Life Sciences. | Worldwide |
| 2,3,4,6-Tetra-O-acetyl-a-D-galactopyranosyl chloride | 2,3,4,6-Tetra-O-acetyl-α-D-galactopyranosyl chloride, an essential compound employed in the biomedical sector, holds paramount significance in the synthesis of carbohydrates, including proteoglycans and glycolipids. Its prospective role extends to the creation of pharmaceuticals targeting ailments associated with carbohydrate metabolism disorders. Furthermore, it serves as a valuable tool in investigating cellular interactions and signaling pathways, unraveling crucial insights in the realm of scientific research. Synonyms: 1-Chloro-2,3,4,6-tetra-o-acetyl-a-D-galactopyranose. CAS No. 14227-87-3. Molecular formula: C14H19ClO9. Mole weight: 366.75. | |
| 2,3,4,6-Tetra-O-acetyl-b-D-galactopyranosyl isothiocyanate | 2,3,4,6-Tetra-O-acetyl-b-D-galactopyranosyl isothiocyanate is a biomedicine product used in the field of chemical biology. This compound acts as a reagent for the selective labeling and modification of carbohydrates containing primary amines. It finds application in the study of glycoproteins, glycolipids, and other biomolecules involved in cellular processes. This product is indispensable in research related to carbohydrate-based therapeutics and drug design. Synonyms: 2,3,4,6-Tetra-O-acetyl-b-D-galactopyranosyl isothiocyanate; 41135-18-6; [(2R,3S,4S,5R,6R)-3,4,5-triacetyloxy-6-isothiocyanatooxan-2-yl]methyl acetate; SCHEMBL5489564; W-202694; 2,3,4,6-Tetra-O-acetyl-.beta.-D-galactopyranosyl isothiocyanate; [(2R,3S,4S,5R,6R)-3,4,5-triacetoxy-6-isothiocyanato-tetrahydropyran-2-yl]methyl acetate. CAS No. 41135-18-6. Molecular formula: C15H19NO9S. Mole weight: 389.38. | |
| 2,3,4,6-Tetra-O-benzyl-L-mannopyranose | 2,3,4,6-Tetra-O-benzyl-L-mannopyranose, a chemical entity, is widely employed as a reagent in the synthesis of diverse glycoconjugates including, but not limited to, glycoproteins and glycolipids. It finds significant usage in the development of potential vaccines and drug delivery systems, aimed at targeting and remediation of pathologies linked with carbohydrate metabolism. With its broad applicability in diverse scientific domains, this compound has emerged as a crucial tool in glycochemistry research. Synonyms: 2,3,4,6-Tetra-O-benzyl-L-mannopyranose; 103368-00-9. CAS No. 103368-00-9. Molecular formula: C34H36O6. Mole weight: 540.7. | |
| 2,3,4,6-Tetra-O-pivaloyl-a-D-mannopyranosyl bromide | 2,3,4,6-Tetra-O-pivaloyl-α-D-mannopyranosyl bromide, a chemical compound, serves as a glycosyl donor for synthesizing glycoconjugates. Due to its versatility, it has been utilized for synthesizing oligosaccharides, glycoproteins, and glycolipids. Additionally, it holds immense therapeutic potential for treating infectious diseases and cancer. Synonyms: [(2R,3R,4S,5S,6R)-6-bromo-3,4,5-tris(2,2-dimethylpropanoyloxy)tetrahydropyran-2-yl]methyl 2,2-dimethylpropanoate. CAS No. 1360879-08-8. Molecular formula: C26H43BrO9. Mole weight: 579.52. | |
| 2,3,4-Tri-O-acetyl-a-L-rhamnopyranosyl azide | 2,3,4-Tri-O-acetyl-α-L-rhamnopyranosyl azide, a vital chemical agent, is extensively employed in the fabrication of glycoconjugates - glycopeptides and glycolipids, among others. Moreover, its role in the comprehensive elucidation of the metabolic pathways and biosynthesis of oligosaccharides cannot be discounted. Its utilization in these domains holds significant implications for the progression of biomedical research, providing insights into the structural and functional attributes of biomolecules. Synonyms: 2,3,4-TRI-O-ACETYL-ALPHA-L-RHAMNOPYRANOSYL AZIDE. Grade: 95%. CAS No. 95580-90-8. Molecular formula: C12H17N3O7. Mole weight: 315.28. | |
| 2,3,4-Tri-O-acetyl-b-L-fucopyranosyl dibenzyl phosphate | 2,3,4-Tri-O-acetyl-b-L-fucopyranosyl dibenzyl phosphate, a derivative of phosphorylated fucoside, is often employed in the production of glycolipids and glycoproteins. This compound displays a remarkable ability to selectively suppress specific fucosylated glycoenzymes that fuel tumor growth and metastasis, marking it as an excellent candidate for potential cancer therapies. Synonyms: [(2S,3R,4R,5S,6R)-4,5-Diacetyloxy-6-bis(phenylmethoxy)phosphoryloxy-2-methyloxan-3-yl] acetate; 6-Deoxy-beta-L-galactopyranose 2,3,4-triacetate 1-[bis(phenylmethyl) phosphate]; (2R,3S,4R,5R,6S)-2-((bis(benzyloxy)phosphoryl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triyl triacetate; SCHEMBL9300189; |A-L-Galactopyranose, 6-deoxy-, 2,3,4-triacetate 1-[bis(phenylmethyl) phosphate]; A889013; beta-L-Galactopyranose, 6-deoxy-, 2,3,4-triacetate 1-[bis(phenylmethyl) phosphate]; (2R,3S,4R,5R,6S)-4,5-bis(acetyloxy)-2-{[bis(benzyloxy)phosphoryl]oxy}-6-methyloxan-3-yl acetate. CAS No. 128473-05-2. Molecular formula: C26H31O11P. Mole weight: 550.49. | |
| 2-Acetamido-1,3,6-tri-O-acetyl-2-deoxy-a-D-glucopyranose | N-Acetylglucosamine triacetate, a derivative of 2-deoxyglucose, is a ubiquitous compound within the biomedical industry employed as a crucial precursor for the synthesis of diverse glycosylated molecules, including glycoproteins and glycolipids. Furthermore, it has demonstrated promising therapeutic effects in conditions such as osteoarthritis and inflammatory bowel disease by modulating cellular signaling pathways vital to their pathogenesis, collectively underscoring its therapeutic value. CAS No. 73024-74-5. Molecular formula: C14H21NO9. Mole weight: 347.32. | |
| 2-Acetamido-2-deoxy-6-O-(2-acetamido-2-deoxy-α-D-glucopyranosyl)-α-D-galactopyranose | 2-Acetamido-2-deoxy-6-O-(2-acetamido-2-deoxy-α-D-glucopyranosyl)-α-D-galactopyranose is a vital compound used in biomedicine. It plays a crucial role as a building block for the synthesis of glycoconjugates. This compound has potential applications in the development of glycolipid-based vaccines and glycoprotein research. Its unique structure enables it to be utilized in the study of glycosylation-related diseases and drug discovery targeting glycan-mediated processes. Synonyms: GlcNAc-a1,6-GalNAc; 2-(Acetylamino)-6-O-[2-(acetylamino)-2-deoxy-α-D-glucopyranosyl]-2-deoxy-α-D-galactopyranose; N-((2S,3R,4R,5S,6R)-2-(((2R,3R,4R,5R,6S)-5-Acetamido-3,4,6-trihydroxytetrahydro-2H-pyran-2-yl)methoxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide. CAS No. 1504562-14-4. Molecular formula: C16H28N2O11. Mole weight: 424.40. | |
| 2-Acetamido-2-deoxy-L-lyxojirimycin | 2-Acetamido-2-deoxy-L-lyxojirimycin, a potent glycosidase inhibitor, is valuable in the remediation of enzyme deficiency-related ailments like Gaucher's and Pompe disease. Its mechanism of action entails lysosomal reduction of glycolipid and glycogen build-up, which results in favorable symptomatology. This chemical entity optimizes treatment efficacy and is a promising therapeutic option for patients with said diseases. CAS No. 1207675-21-5. Molecular formula: C7H14N2O3. Mole weight: 174.20. | |
| 2-Acetamido-3,4,6-tri-O-acetyl-1-O-[(N-Cbz-aminoethoxy)ethoxy]-2-deoxy-b-D-galactopyranose | 2-Acetamido-3,4,6-tri-O-acetyl-1-O-[(N-Cbz-aminoethoxy)ethoxy]-2-deoxy-b-D-galactopyranose, a carbohydrate derivative, has found its potential significance in the biomedical sector for exploring glycolipids and their intricacies. As an unparalleled tool, it can pave the way for diverse research opportunities in glycosylation disorders and holds promise in discovering new leads for disease intervention, including cancer. The versatility of this compound's glycan structure and its potential therapeutic significance underscore its importance as a compelling research asset. Synonyms: (2R,3R,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-(2-(2-(benzyloxycarbonylamino)ethoxy)ethoxy)tetrahydro-2H-pyran-3,4-diyl diacetate; 2-(Benzyloxycarbonylamino)ethoxy)ethoxy 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-D-galactopyranoside; Carbamic acid, N-[2-[2-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]ethoxy]ethyl]-, phenylmethyl ester; Phenylmethyl N-[2-[2-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]ethoxy]ethyl]carbamate; 2-Acetamido-3,4,6-tri-O-acetyl-1-O-[(N-Cbz-aminoethoxy)ethoxy]-2-deoxy-b-D-galactopyranose. Grade: ≥95%. CAS No. 1261568-35-7. Molecular formula: C26H36N2O12. Mole weight: 568.57. | |
| 2-Acetamido-6-O-(2-acetamido-2-deoxy-a-D-galactopyranosyl)-2-deoxy-D-galactopyranose | 2-Acetamido-6-O-(2-acetamido-2-deoxy-a-D-galactopyranosyl)-2-deoxy-D-galactopyranose is a vital compound used in biomedicine. It plays a crucial role as a building block for the synthesis of glycoconjugates. This compound has potential applications in the development of glycolipid-based vaccines and glycoprotein research. Its unique structure enables it to be utilized in the study of glycosylation-related diseases and drug discovery targeting glycan-mediated processes. Synonyms: GalNAc-a1,6-GalNAc; 2-(Acetylamino)-6-O-[2-(acetylamino)-2-deoxy-α-D-galactopyranosyl]-2-deoxy-D-galactopyranose; GalNAc(a1-6)GalNAc; 2-Acetamido-2-deoxy-alpha-D-galacto-hexopyranosyl-(1->6)-2-acetamido-2-deoxy-D-galacto-hexopyranose; N-((2S,3R,4R,5R,6R)-2-(((2R,3R,4R,5R)-5-Acetamido-3,4,6-trihydroxytetrahydro-2H-pyran-2-yl)methoxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide. Molecular formula: C16H28N2O11. Mole weight: 424.40. | |
| 2-Azidoethyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 2-Azidoethyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a versatile compound widely used in the biomedical industry. It serves as a valuable tool in drug discovery and development, specifically for synthesizing new carbohydrate-based antibiotics and antiviral drugs. Additionally, this compound is employed in research related to glycobiology and molecular biology, aiding in the study of glycoproteins and glycolipids involved in various diseases, including cancer and infectious diseases. Synonyms: Azidoethyl N-Acetyl-b-D-glucosaminide; beta-D-Glucopyranoside, 2-azidoethyl 2-(acetylamino)-2-deoxy-; N-Acetyl-1-O-(2-azidoethyl)-beta-D-glucosamine; beta-GlcNAc-N3; 1-(2-Azidoethoxy)-2-acetamido-2deoxy-beta-D-glucopyranoside. Grade: ≥98% by HPLC. CAS No. 142072-12-6. Molecular formula: C10H18N4O6. Mole weight: 290.27. | |
| 2-Benzamido-2-deoxy-D-glucopyranose (α/β mixture) | 2-Benzamido-2-deoxy-D-glucopyranose (α/β mixture) is an intriguing compound widely employed in the realm of biomedicine due to its multifarious pharmacological applications. Its unique composition, comprising both α and β isomers, renders it an indispensable foundational entity for synthesizing glycolipids, glycopeptides is and glycoconjugates. Its ability to undergo structural modifications endows it with significant value in combating diseases associated with carbohydrate metabolism and glycan signaling pathways. Synonyms: 2-(Benzoylamino)-2-deoxy-D-glucopyranose. Grade: 98%. CAS No. 14086-91-0. Molecular formula: C13H17NO6. Mole weight: 283.28. | |
| 2-(Benzyloxycarbonylamino)-2-deoxy-D-mannose | 2-(Benzyloxycarbonylamino)-2-deoxy-D-mannose, a saccharide molecule found in the biomedical sector, serves as a key building block for the fabrication of glycolipids and glycoproteins by aiding in the production of glycoconjugates. It is also utilized as a fundamental substrate in the synthesis of numerous sugar analogues, highlighting its versatility in chemical processes. The exceptional utility of this carbohydrate compound emphasizes its significance in the fields of chemical biology and medicinal chemistry. Synonyms: 2-(Benzyloxycarbonylamino)-2-deoxy-D-mannose; 1174233-24-9; D-Mannose, 2-deoxy-2-[[(phenylmethoxy)carbonyl]amino]-; benzyl N-[(2S,3R,4S,5R)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl]carbamate; Benzyl ((2S,3R,4S,5R)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl)carbamate; 2-(Benzyloxycarbonylamino)-2-deoxy-D-glucose; SCHEMBL8822978; 16684-31-4. CAS No. 1174233-24-9. Molecular formula: C14H19NO7. Mole weight: 313.31. | |
| 2-Bromoethyl a-L-fucopyranoside | 2-Bromoethyl α-L-fucopyranoside, a glycosylation reagent regularly employed in biochemical research, is a compound of utmost importance. By synthesizing glycans and glycoconjugates containing fucose, cellular processes such as immunity, signaling, and adhesion can be thoroughly investigated. Additionally, it functions as a fundamental building block for synthesizing glycolipids and glycopeptides, paving the way for advanced research in various fields. Molecular formula: C8H15BrO5. Mole weight: 271.11. | |
| 2'-(N-Hexadecanoylamino)-4'-nitrophenyl-b-D-galactopyranoside | 2'-(N-Hexadecanoylamino)-4'-nitrophenyl-b-D-galactopyranoside, a substrate well-known for its use in enzymatic assays to test β-galactosidase activity, stands tall. Its applications also extend to the study of lipid-modifying enzymes and glycolipid metabolism. Synonyms: N-[2-(β-D-Galactopyranosyloxy)-5-nitrophenyl]hexadecanamide; 2-Hexadecanoylamino-4-nitrophenyl β-D-galactopyranoside. CAS No. 63424-42-0. Molecular formula: C28H46N2O9. Mole weight: 554.67. | |
| 3,4,6-Tri-O-benzyl-2-deoxy-2-phthalimdo-b-D-glucopyranosyl azide | 3,4,6-Tri-O-benzyl-2-deoxy-2-phthalimdo-b-D-glucopyranosyl azide is a potent compound serving as a key intermediate for the research and development of glycopeptides and glycolipids for therapeutic purposes. With its unique azide group, this compound enables efficient and selective bioconjugation for drug delivery systems, targeted cancer therapy, and diagnostic imaging applications in the reserch of various diseases. Molecular formula: C35H32N4O6. Mole weight: 604.65. | |
| 3-Aminopropyl b-D-galactopyranoside | 3-Aminopropyl b-D-galactopyranoside is a valuable compound commonly used as a glycosylation compound and chaperone in various biochemistry studies. This compound serves as a precursor for the research and development of glycolipids and glycoproteins. Additionally, it has been employed to investigate lectin-carbohydrate interactions. Molecular formula: C9H19NO6. Mole weight: 237.25. | |
| 3-Galactosyl-N-acetyl-D-lactosamine | 3-Galactosyl-N-acetyl-D-lactosamine is an essential constituent in glycoprotein and glycolipid bioresearch and development assuming a pivotal function in mediating cell-cell adhesion, cellular interactions and vital cell signaling events. Revered within the biomedical realm, this compound facilitates the comprehensive exploration of glycans' structural and functional aspects, thereby unraveling their intricate involvement in manifold afflictions, existing as cancer, inflammation and autoimmune disorders. Synonyms: Galb1-3Galb1-4GlcNAc. | |
| 3-galactosyl-N-acetylglucosaminide 4-α-L-fucosyltransferase | This enzyme is the product of the Lewis blood group gene. Normally acts on a glycoconjugate where R (see reaction) is a glycoprotein or glycolipid. Although it is a 4-fucosyltransferase, it has a persistent 3-fucosyltransferase activity towards the glucose residue in free lactose. This enzyme fucosylates on O-4 of an N-acetylglucosamine that carries a galactosyl group on O-3, unlike EC 2.4.1.152, 4-galactosyl-N-acetylglucosaminide 3-α-L-fucosyltransferase, which fucosylates on O-3 of an N-acetylglucosamine that carries a galactosyl group on O-4. Enzymes catalysing the 4-α-fucosylation of the GlcNAc in β-D-Gal-(1?3)-β-GlcNAc sequences (with some activity also as 3-α-fucosyltransferases) are present in plants, where the function in vivo is the modification of N-glycans. In addition, the fucTa gene of Helicobacter strain UA948 encodes a fucosyltransferase with both 3-α- and 4-α-fucosyltransferase activities. Group: Enzymes. Synonyms: (Lea)-dependent (α-3/4)-fucosyltransferase; α(1,3/1,4) fucosyltransferase III; α-(1?4)-L-fucosyltransferase; α-4-L-fucosyltransferase; β-acetylglucosaminylsaccharide fucosyltransferase; FucT-II; Lewis α-(1?3/4)-fucosyltransferase; Lewis blood group α-(1?3/4)-fucosyltransferase; Lewis(Le) blood . Enzyme Commi | |
| 4,6-O-Benzylidene-1,2,3-tri-O-pivaloyl-b-D-galactopyranose | 4,6-O-Benzylidene-1,2,3-tri-O-pivaloyl-b-D-galactopyranose is a remarkably intricate and versatile molecule, assuming a vital position in research of a myriad of ailments. Chief among its utility is the targeted intervention on glycosylated compounds, encompassing glycoproteins and glycolipids, crucially implicated in afflictions ranging from malignant neoplasms to infectious maladies and sundry disorders. Molecular formula: C28H40O9. Mole weight: 520.63. | |
| 4-galactosyl-N-acetylglucosaminide 3-α-L-fucosyltransferase | Normally acts on a glycoconjugate where R (see reaction) is a glycoprotein or glycolipid. This enzyme fucosylates on O-3 of an N-acetylglucosamine that carries a galactosyl group on O-4, unlike EC 2.4.1.65, 3-galactosyl-N-acetylglucosaminide 4-α-L-fucosyltransferase, which fucosylates on O-4 of an N-acetylglucosamine that carries a galactosyl group on O-3. Group: Enzymes. Synonyms: Lewis-negative α-3-fucosyltransferase; plasma α-3-fucosyltransferase; guanosine diphosphofucose-glucoside α1?3-fucosyltransferase; galactoside 3-fu. Enzyme Commission Number: EC 2.4.1.152. CAS No. 39279-34-0. 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-2378; 4-galactosyl-N-acetylglucosaminide 3-α-L-fucosyltransferase; EC 2.4.1.152; 39279-34-0; Lewis-negative α-3-fucosyltransferase; plasma α-3-fucosyltransferase; guanosine diphosphofucose-glucoside α1?3-fucosyltransferase; galactoside 3-fucosyltransferase; GDP-L-fucose:1,4-β-D-galactosyl-N-acetyl-D-glucosaminyl-R 3-L-fucosyltransferase; GDP-β-L-fucose:1,4-β-D-galactosyl-N-acetyl-D-glucosaminyl-R 3-L-fucosyltransferase; GDP-β-L-fucose:1,4-β-D-galactosyl-N-acetyl-D-glucosaminyl-R 3-α-L-fucosyltransferase. Cat No: EXWM-2378. | |
| 4-Methylphenyl 2-O-benzoyl-3,6-di-O-benzyl-4-O-(9-fluorenylmethoxycarbonyl)-1-thio-β-D-galactopyranoside | 4-Methylphenyl 2-O-benzoyl-3,6-di-O-benzyl-4-O-(9-fluorenylmethoxycarbonyl)-1-thio-β-D-galactopyranoside is a compound extensively utilized in the field of biomedical research, serving as a pivotal compound in glycosylation reactions, offering a versatile platform for the research and development of diverse glycoproteins and glycolipids. Synonyms: β-D-Galactopyranoside, 4-methylphenyl 3,6-bis-O-(phenylmethyl)-1-thio-, 2-benzoate 4-(9H-fluoren-9-ylmethyl carbonate). CAS No. 2088577-19-7. Molecular formula: C49H44O8S. Mole weight: 792.94. | |
| 4-Nitrophenyl b-globo-N-tetraoside | 4-Nitrophenyl b-globo-N-tetraoside is a valuable compound widely used in the biomedical industry. This product acts as a substrate for enzymes involved in the degradation of glycolipids, playing a crucial role in studies related to lysosomal storage diseases. Its ability to mimic glycolipid structures aids in investigating disease mechanisms and developing potential therapeutic strategies. Synonyms: GalNAc-b-1,3-Gal-a-1,4-Gal-b-1,4-Glc-b-pNP; 4-Nitrophenyl O-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl-(1→3)-O-α-D-galactopyranosyl-(1→4)-O-β-D-galactopyranosyl-(1→4)-β-D-glucopyranoside; GalNAc(b1-3)Gal(a1-4)Gal(b1-4)Glc(b)-O-Ph(4-NO2); Gb4-β-pNP; GalNAcβ(1-3)Galα(1-4)Galβ(1-4)Glc-β-pNP. CAS No. 1134635-03-2. Molecular formula: C32H48N2O23. Mole weight: 828.72. | |
| 5-Fluorouridine 5'-Diphosphate Galactose | 5-Fluorouridine 5'-Diphosphate Galactose is a crucial molecule in biomedicine used for treating certain diseases. It plays a vital role as a competitive inhibitor of UDP-galactose 4-epimerase, which is involved in the synthesis of glycoproteins and glycolipids. This product finds applications in the development of targeted therapies for cancer, as it acts by inhibiting the galactosylation process essential for tumor growth and metastasis. Synonyms: Fudp-5. CAS No. 92748-40-8. Molecular formula: C15H23FN2O17P2. Mole weight: 584.29. | |
| 5'-GalNAc C3 Phosphoramidite | 5'-GalNAc C3 Phosphoramidite is a specialized reagent used in oligonucleotide synthesis to introduce N-acetylgalactosamine (GalNAc) at the 5'-end of the oligonucleotide sequence. GalNAc is a carbohydrate moiety commonly found in glycoproteins and glycolipids and is involved in various biological processes, including cell signaling and immune response modulation. By attaching GalNAc to oligonucleotides, researchers can develop molecular probes and therapeutics targeting specific carbohydrate-binding proteins, such as lectins and receptors. This modification enables the study of carbohydrate-protein interactions and the development of oligonucleotide-based drugs for therapeutic applications, including gene regulation, RNA interference, and targeted delivery. Synonyms: Phosphoramidous acid, N,N-bis(1-methylethyl)-, 2-cyanoethyl [1-[1-oxo-6-[[1-oxo-4-[[3,4,6-tri-O-acetyl-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]oxy]butyl]amino]hexyl]-4-[[tris(4-methoxyphenyl)methoxy]methyl]-4-piperidinyl]methyl ester; (2R,3R,4R,5R,6R)-5-Acetamido-2-(acetoxymethyl)-6-(4-((6-(4-((((2-cyanoethoxy)(diisopropylamino)phosphaneyl)oxy)methyl)-4-((tris(4-methoxyphenyl)methoxy)methyl)p. Grade: >98%. CAS No. 2437303-51-8. Molecular formula: C62H88N5O17P. Mole weight: 1206.36. | |
| 6-a-Sialyl-N-acetyllactosamine-PAA-biotin | 6-a-Sialyl-N-acetyllactosamine-PAA-biotin is a groundbreaking and indispensable compound, facilitating the study of glycoproteins and glycolipids' sialylation processes. This extraordinary compound manifests as a meticulously engineered ligand, exhibiting exceptional selectivity towards lectins and antibodies that essentially target sialic acid residues. Synonyms: Neu5Ac-a-2-6-Gal-b-1-4-GlcNAc-O(CH2)3-PAA-(CH2)6-biotin; 6-SLN-biotin. | |
| 6-Deoxy-L-altrose | 6-Deoxy-L-altrose, a scarce sugar, has gained an esteemed place in the biomedical research community due to its ability to probe glycoproteins and glycolipids. Additionally, research has discovered its manifold potential in treating MRSA infections as well as in fighting inflammation. The peculiarity in its constitution offers diverse prospects in drug design as well as in exploring carbohydrate-related pathologies. Synonyms: 6-Deoxyaltrose; 18546-02-6; 6-Deoxy-L-altrose; (2S,3R,4R,5R)-2,3,4,5-tetrahydroxyhexanal; 6-DEOXY-D-ALTROSE; D-Altrose, 6-deoxy-; SCHEMBL1458729; DTXSID20171781. CAS No. 18546-02-6. Molecular formula: C6H12O5. Mole weight: 164.16. | |
| 7DW8-5 | 7DW8-5, a novel glycolipid, an analog of α-galactosylceramide (α-GalCer), is an immunostimulate iNKT agonist and a vaccine adjuvant that can harness and amplify the immunotherapeutic potential of NKT cells to treat certain microbial infections such as malaria and HIV. Studies have shown that the adjuvant effect of 7DW8-5 wasmediated by CD1dmolecules. Synonyms: [(2S,3S,4R)-1-O-(α-D-galactopyranosyl)-N-(11-(4-fluorophenyl)undecanoyl)-2-amino-1,3,4-octadecanetriol)]; N-[(2S,3S,4R)-3,4-dihydroxy-1-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadecan-2-yl]-11-(4-fluorophenyl)undecanamide; 11-(4-Fluorophenyl)-N-[(2s,3s,4r)-1-(Alpha-D-Galactopyranosyloxy)-3,4-Dihydroxyoctadecan-2-Yl]undecanamide; CHEBI:86489; 7DW8-5; 7DW. CAS No. 1056025-00-3. Molecular formula: C41H72FNO9. Mole weight: 742. | |
| 9-Amino-N-acetylneuraminic acid | 9-Amino-N-acetylneuraminic acid, a remarkable biomedicine product, holds immense potential in combating various diseases and disorders. By serving as a precursor for sialic acid synthesis, it facilitates the formation of crucial glycoproteins and glycolipids. This product assumes a pivotal role in multifaceted biological mechanisms, encompassing cellular communication, immunological responses, and viral infection pathways. Synonyms: N-Acetyl-9-amino-9-deoxyneuraminic Acid; 5-N-acetyl-9-amino-9-deoxy neuraminic acid; 5-(Acetylamino)-9-amino-3,5,9-trideoxy-D-glycero-D-galacto-2-nonulosonic acid. CAS No. 112037-47-5. Molecular formula: C11H20N2O8. Mole weight: 308.29. | |
| acyl-[acyl-carrier-protein]-UDP-N-acetylglucosamine O-acyltransferase | Involved with EC 2.4.1.182 (lipid-A-disaccharide synthase) and EC 2.7.1.130 (tetraacyldisaccharide 4'-kinase) in the biosynthesis of the phosphorylated glycolipid, Lipid A, in the outer membrane of Escherichia coli. Group: Enzymes. Synonyms: UDP-N-acetylglucosamine acyltransferase; uridine diphosphoacetylglucosamine acyltransferase; acyl-[acyl-carrier-protein]-UDP-N-acetylglucosamine O-acyltransferase; (R)-3-hydroxytetradecanoyl-[acyl-carrier-protein]:UDP-N-acetylglucosamine 3-O-(3-hydroxytetradecanoyl)transferase. Enzyme Commission Number: EC 2.3.1.129. CAS No. 105843-69-4. 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-2066; acyl-[acyl-carrier-protein]-UDP-N-acetylglucosamine O-acyltransferase; EC 2.3.1.129; 105843-69-4; UDP-N-acetylglucosamine acyltransferase; uridine diphosphoacetylglucosamine acyltransferase; acyl-[acyl-carrier-protein]-UDP-N-acetylglucosamine O-acyltransferase; (R)-3-hydroxytetradecanoyl-[acyl-carrier-protein]:UDP-N-acetylglucosamine 3-O-(3-hydroxytetradecanoyl)transferase. Cat No: EXWM-2066. | |
| α(1-3,4,6) Galactosidase from Green coffee bean, 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). Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. GLA. Mole weight: 39700 daltons. Activity: 71,000 units/mg. Storage: 4°C. Form: 20 mM Tris-HCl (pH 7.5), 50 mM NaCl and 1 mM EDTA. Source: E. coli. Species: Green coffee bean. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α(1-3,4,6) Galactosidase. Cat No: NATE-1263. | |
| α(1-3,6) Galactosidase from Xanthomonas manihotis, 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). Α1-3,6 galactosidase is a highly specific exoglycosidase that catalyzes the hydrolysis of α1-3 and α1-6 linked d-galactopyranosyl residues from oligosaccharides. Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Purity: > 95% determined by SDS-PAGE. GLA. Mole weight: 70000 daltons. Activity: 137,000 units/mg. Storage: Recommended storage temperature is 4°C. Avoid repeated freeze/thaw cycles. Form: 50 mM NaCl, 20 mM Tris-HCl (pH 7.5 25°C) and 1 mM Na2EDTA. Source: E. coli. Species: Xanthomonas manihotis. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α(1-3,6) Galactosidase. Cat No: NATE-1279. | |
| α-2,3/8-sialyltransferase from Campylobacter jejuni, Recombinant | Sialyltransferases are enzymes that transfer sialic acid to nascent oligosaccharide. Each sialyltransferase is specific for a particular sugar substrate. Sialyltransferases add sialic acid to the terminal portions of the sialylated glycolipids (gangliosides) or to the N-or O-linked sugar chains of glycoproteins. Sialyltransferases belong to glycosyltransferase family 29 (CAZY GT_29) which use a nucleotide monophosphosugar as the donor (CMP-NeuA) instead of a nucleotide diphosphosugar. Group: Enzymes. Synonyms: α (2,3)-Sialyltransferase; Beta-galactoside alpha-2,3-sialyltransferase; Beta-galactosamide alpha-2,3-sialyltransferase; CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase. Enzyme Commission Number: EC 2.4.99.-. Purity: min 95% by SDS-PAGE. α-Sialyltransferase. Mole weight: 31 kDa. Source: E. coli. Species: Campylobacter jejuni. α (2,3)-Sialyltransferase; Beta-galactoside alpha-2,3-sialyltransferase; Beta-galactosamide alpha-2,3-sialyltransferase; CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase; α-2,3/8-sialyltransferase; EC 2.4.99.-. Cat No: NATE-1476. | |
| α-2,3-Sialyltransferase from Pasteurella multocida, Recombinant | Sialyltransferases are enzymes that transfer sialic acid to nascent oligosaccharide. Each sialyltransferase is specific for a particular sugar substrate. Sialyltransferases add sialic acid to the terminal portions of the sialylated glycolipids (gangliosides) or to the N-or O-linked sugar chains of glycoproteins. Sialyltransferases belong to glycosyltransferase family 29 (CAZY GT_29) which use a nucleotide monophosphosugar as the donor (CMP-NeuA) instead of a nucleotide diphosphosugar. Group: Enzymes. Synonyms: α (2,3)-Sialyltransferase; Beta-galactoside alpha-2,3-sialyltransferase; Beta-galactosamide alpha-2,3-sialyltransferase; CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase. Enzyme Commission Number: EC 2.4.99.4. CAS No. 71124-51-1. α-Sialyltransferase. Mole weight: 46.4 kDa. Activity: > 2 units/mg. Storage: Store the product at -20 °C. It remains active for at least 1 year when stored properly. Form: Lyophilized powder containing Tris-HCl and NaCl. Source: E. coli BL21. Species: Photobacterium damsela. α (2,3)-Sialyltransferase; Beta-galactoside alpha-2,3-sialyltransferase; Beta-galactosamide alpha-2,3-sialyltransferase; CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase. Cat No: NATE-1171. | |
| α-2,3-Sialyltransferase, pasteurella multocida | alpha-2,3-Sialyltransferase (PmST3) (EC 2.4.99.4) is a beta-galactoside. alpha-2,3-Sialyltransferase (PmST3) catalyzes the transfer of sialic acid to carbohydrate groups of glycoproteins and glycolipids [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Fh8-PmST3. CAS No. 71124-51-1. Pack Sizes: 50 U. Product ID: HY-E70062. |  |
| α-2,3-Sialyltransferase, Recombinant | Sialyltransferases are enzymes that transfer sialic acid to nascent oligosaccharide. Each sialyltransferase is specific for a particular sugar substrate. Sialyltransferases add sialic acid to the terminal portions of the sialylated glycolipids (gangliosides) or to the N-or O-linked sugar chains of glycoproteins. Sialyltransferases belong to glycosyltransferase family 29 (CAZY GT_29) which use a nucleotide monophosphosugar as the donor (CMP-NeuA) instead of a nucleotide diphosphosugar. Α-2,3-sialyltransferase is used for in vitro sialylation of all galβ1-4glcnac units on glycoproteins, such as monoclonal antibodies (mabs). clear colorless to slightly colored so...d. Group: Enzymes. Synonyms: α (2,3)-Sialyltransferase; Beta-galactoside alpha-2,3-sialyltransferase; Beta-galactosamide alpha-2,3-sialyltransferase; CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase. Purity: > 90%. α-Sialyltransferase. Mole weight: 34.5 kDa. Activity: > 80 U/ug (1 Unit = pmol / min, using 10 ug enzyme in Sialyltransferase activity assay). Stability: at -15°C to -25°C: within specification range for 12 months. Appearance: clear, colorless to slightly colored solution. α-2,3-Sialyltransferase; α (2,3)-Sialyltransferase; Beta-galactoside alpha-2,3-sialyltransferase; Beta-galactosamide alpha-2,3-sialyltransferase | |
| α(2,6)-Sialyltransferase from Photobacterium damsela, Recombinant | Sialyltransferases are enzymes that transfer sialic acid to nascent oligosaccharide. Each sialyltransferase is specific for a particular sugar substrate. Sialyltransferases add sialic acid to the terminal portions of the sialylated glycolipids (gangliosides) or to the N-or O-linked sugar chains of glycoproteins. Sialyltransferases belong to glycosyltransferase family 29 (CAZY GT_29) which use a nucleotide monophosphosugar as the donor (CMP-NeuA) instead of a nucleotide diphosphosugar. Sialyltransferase transfers Neu5Ac from CMP-Neu5Ac to the galactosyl terminus of acceptor molecules including glycoproteins, glycolipids, and oligosaccharides. Applications: ...lactosamide-alpha-2,6-sialyltransferase; ST6Gal1; EC 2.4.99.1. Enzyme Commission Number: EC 2.4.99.1. CAS No. 9075-81-4. α-Sialyltransferase. Mole weight: 56.8 kDa. Activity: > 5 units/mg protein. Stability: Store the product at -20 °C. It remains active for at least 1 year when stored properly. Form: Supplied as a lyophilized powder containing Tris-HCl and NaCl. Source: E. coli BL21. Species: Photobacterium damsela. α(2,6)-Sialyltransferase; Beta-galactoside alpha-2,6-sialyltransferase; Beta-galactosamide alpha-2,6-sialyltransferase; CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,6-sialyltransferase; ST6Gal1; EC 2.4.99.1. Cat No: NATE-0759. | |
| α-Galactosidase 110A from Bacteroides fragilis, 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). 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.-. CAS No. 9025-35-8. Purity: >90% by SDS-PAGE. GLA. Mole weight: 67.9 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 fragilis. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 110A. Cat No: NATE-1405. | |
| α-Galactosidase 110A from Bacteroides thetaiotaomicron, 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). 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. Purity: >50% by SDS-PAGE. GLA. Mole weight: 65.1 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: Bacteroides thetaiotaomicron. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 110A. Cat No: NATE-1403. | |
| α-Galactosidase 27A from Clostridium cellulolyticum, 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). 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. Purity: >90% by SDS-PAGE. GLA. Mole weight: 44.0 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: Clostridium cellulolyticum. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 27A. Cat No: NATE-1400. | |
| α-Galactosidase 4A from Bacillus halodurans, 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). 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. Purity: >90% by SDS-PAGE. GLA. Mole weight: 51.8 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 halodurans. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 27A. Cat No: NATE-1404. | |
| α-Galactosidase 95A from Bacteroides ovatus, 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). 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. Purity: >90% by SDS-PAGE. GLA. Mole weight: 91 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 ovatus. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 95A. Cat No: NATE-1406. | |
| α-Galactosidase 97A from Bacteroides thetaiotaomicron, 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). 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. Purity: >50% by SDS-PAGE. GLA. Mole weight: 74.7 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. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 97A. Cat No: NATE-1402. | |
| α-Galactosidase 97B from Bacteroides thetaiotaomicron, 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). 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. Purity: >90% by SDS-PAGE. GLA. Mole weight: 74.9 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. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 97B. Cat No: NATE-1401. | |
| α-Galactosidase, Aspergillus niger | α-Galactosidase, Aspergillus niger (EC 3.2.1.22), that is, α-galactosidase, is a glycoside hydrolase that widely exists in animals, plants and microorganisms, and is often used in biochemical research. α-Galactosidase catalyzes the hydrolysis of α-1,6-linked terminal galactose residues, including galactooligosaccharides, galactomannans, and galactolipids. Catalyzes many catabolic processes including cleavage of glycoproteins, glycolipids and polysaccharides [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EC 3.2.1.22. CAS No. 9025-35-8. Pack Sizes: 5 g; 10 g. Product ID: HY-P2871. | |
| α-Galactosidase from Cellvibrio mixtus, 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). 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. Purity: > 95 % as judged by SDS-PAGE. GLA. Mole weight: 44582.3 Da. Activity: 150 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Lyophilised powder. Source: Cellvibrio mixtus ATCC 12120. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Cat No: NATE-1175. | |
| α-Galactosidase from Clostridium cellulolyticum, 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). 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. Purity: > 95 % as judged by SDS-PAGE. GLA. Mole weight: 64179.5 Da. Activity: 186.7 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Clostridium cellulolyticum H10. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Cat No: NATE-1176. | |
| 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. | |
| α-Galactosylceramide | α-Galactosylceramide (α-GalCer) is a synthetic glycolipid with antitumorial and immunostimulatory. α-Galactosylceramide is a very potent NKT cell agonist and binds effectively to CD1d. The complex of α-Galactosylceramide plus CD1d binds the NKT cell TCR (T cell antigen receptor) [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: α-GalCer; KRN7000. CAS No. 158021-47-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-102022. | |
| Anionic Surfactant | Anionic surfactant is an incredibly versatile biosurfactant utilizing the unique properties of sophorolipids (SLP) in the glycolipid class. This 100% fermentation-produced solution is TSCA-pending and REACH-registered, making it prime for industrial applications as a dispersant, emulsifier, and wetting agent. Amphi® CH's exceptional attributes include low HLB, low to no foam, hydrophobicity, and excellent degreasing abilities. Additionally, it is USDA-certified, readily biodegradable, and free from prop 65 issues and 1,4-dioxane. Furthermore, it is non-GMO, palm oil-free, and has a low carbon footprint. Uses: Coalescing agent, degreaser, dispersant, dispersant, emulsifier, scouring ...ls - paper & pulp chemicals (finishing additives & treatments). industrial additives & materials - processing aids (polymerization additives). cleaning ingredients - soaps & surfactants (blends & other surfactants). cosmetic ingredients - surfactants & cleansers (blends & other cleansers). industrial additives & materials - textile & leather chemicals (finishing additives & treatments). industrial additives & materials - water treatment chemicals (water treatment additives). Approvals: REACH-registered, USDA-certified 100% BioBased content, Readily Biodegradable. CAS No. Product ID: Amphi® CH. Molecular formula: 1,4-Dioxane-free, 100% Carbon Renewable (RCI), Bio-based, Biodegradable |  |
| Antibiotic L-681,217 (L 681217) | Antibiotic L 681,217 is a glycolipid-type antibiotic related to the efrotomycin class isolated from a Streptomyces sp. It inhibits bacterial protein synthesis at the elongation stage, its target being elongation factor Tu (EF-Tu). Antibiotic L 681,217 also shows broad spectrum antibiotic activity against gram-positive and gram-negative bacteria. Group: Biochemicals. Alternative Names: L 681217. Grades: Highly Purified. CAS No. 93522-10-2. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| archaetidylinositol phosphate synthase | Requires Mg2+ or Mn2+ for activity. The enzyme is involved in biosynthesis of archaetidyl-myo-inositol, a compound essential for glycolipid biosynthesis in archaea. Group: Enzymes. Synonyms: AIP synthase. Enzyme Commission Number: EC 2.7.8.39. 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-3338; archaetidylinositol phosphate synthase; EC 2.7.8.39; AIP synthase. Cat No: EXWM-3338. | |
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