Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| A1F Glycan, 2-AA labelled | A1F Glycan, 2-AA labelled is a specialized product commonly used in the research and development of novel drugs used for the treatment of various types of cancers and autoimmune diseases. This glycan is a modified form of A1F, which has been labelled with a 2-Aminobenzoic acid (2-AA) to enhance its ability to bind to specific receptors and increases bioavailability. Its unique properties make it an essential tool for scientists studying the mechanisms of certain diseases and developing targeted therapies. |  |
| A1F Glycan, 2-AB labelled | A1F Glycan, 2-AB labelled. | |
| A1F Glycan ammonium salt | from Porcine. Group: Fluorescence/luminescence spectroscopy. |  |
| A1F N-Glycan | A1F N-Glycan, the versatile biomolecule employed by the biomedical industry, is the key player in the in-depth scrutiny and diagnosis of diverse disorders - think cancer, Alzheimer's, and rheumatoid arthritis. Its multifaceted involvement in cell signaling pathways has made it a go-to diagnostic marker in countless clinical settings. Furthermore, the therapeutic potential of A1F N-Glycan has not gone unexploited; it forms the crux of several drug formulations aimed at combating these afflictions. Synonyms: Monosialo (2,6), fucosylated biantennary (A1F); A1F glycan; FA2G2S1 Glycan; Mono-sialylated, galactosylated, core-fucosylated, bi-antennary N-linked glycan; Mannotriose-(fucosyl-di-[N-acetylglucosamine]), mono-sialyl-bis(galactosyl-N-acetylglucosaminyl); NeuNAc(Gal-GlcNAc)2Man3(GlcNAc)2Fuc; β-D-Glucopyranose, O-(N-acetyl-α-neuraminosyl)-[2→3(or 2→6)]-O-β-D-galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-O-α-D-mannopyranosyl-[1→3(or 1→6)]-O-[O-β-D-galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-α-D-mannopyranosyl-[1→6(or 1→3)]]-O-β-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→6)]-2-(acetylamino)-2-deoxy-. Grade: ≥90%. CAS No. 571188-30-2. Molecular formula: C79H131N5O58. Mole weight: | |
| A1 Glycan, 2-AA labelled | A1 Glycan, 2-AA labelled, an indispensable instrument for exploring the intricacies of glycans linked to multifarious illnesses, encompassing cancer, Alzheimer's, and autoimmune disorders, is an asset to biomedical research. An integral part of comprehending the biological underpinnings and workings of these ailments, this product is vital in developing efficacious therapies. | |
| A1 Glycan, 2-AB labelled | A1 Glycan, 2-AB labelled. | |
| A1 N-Glycan | A1 N-Glycan is a versatile and Indispensable compound orchestrating numerous vital biological phenomena encompassing the domains of cell adhesion, immune response modulation and the enigmatic journey of disease progression. Synonyms: Monosialo (2,6), biantennary (A1); A1 glycan; A2G2S1 N-Glycan; NeuNAc(Gal-GlcNAc)2Man3(GlcNAc)2; Mono-sialylated, galactosylated, bi-antennary N-linked glycan. Grade: ≥90%. CAS No. 145211-79-6. Molecular formula: C73H121N5O54. Mole weight: 1932.74. | |
| A2B N-Glycan | A2B N-Glycan is a fundamental constituent employed in dissecting intricate glycosylation arrangements. It assumes a pivotal function in developing the formulation of therapeutics directed towards a myriad of ailments such as neoplasms, neurodegenerative maladies like Alzheimer's and immune system dysfunctions. Synonyms: Sialo, bisected, biantennary N-linked glycan. | |
| A2FB N-Glycan | A2FB N-Glycan is an indispensable compound in the biomedical field, playing a significant role in elucidating and deciphering the intricate N-glycosylation profiles discernible in diverse pharmaceuticals and ailments. Synonyms: sialyl, fucosylated, bisected biantennary N-linked glycan. | |
| A2F Glycan, 2-AA labelled | A2F Glycan, 2-AA labelled, a highly specialized chemical utilized in the biomedical industry, possesses immense potential in decoding the intricate processes of glycosylation in the human body, playing a pivotal role in shedding light on several degenerative diseases, including Alzheimer's and Parkinson's. Its effectiveness lies in serving as an indispensable tool in drug development, with its ability to aid in targeting these illnesses. This scientific marvel has indeed revolutionized the study of glycosylation through its unparalleled contributions to medical research and development. | |
| A2F Glycan, 2-AB labelled | A2F Glycan, 2-AB labelled. | |
| A2F Glycan ammonium salt | from porcine thyroglobulin, ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| A2F N-Glycan | A2F N-Glycan is a biomolecule widely found in human cells, involved in glycosylation process. It is commonly used in the biomedicine industry for studying age-related macular degeneration (AMD) as well as other diseases related to glycation, such as Alzheimer's and diabetes. A2F N-Glycan also plays a crucial role in developing therapeutic drugs targeted to these diseases. Synonyms: Disialo, galactosylated, fucosylated, biantennary (A2F); Di-sialylated, galactosylated, core-fucosylated bi-antennary N-linked glycan; FA2G2S2 Glycan; Mannotriose-(fucosyl-di-[N-acetylglucosamine]), bis(sialyl-galactosyl-N-acetylglucosaminyl); (NeuNAc-Gal-GlcNAc)2Man2(Fuc)(GlcNAc)2; A2F glycan; O-(N-Acetyl-α-neuraminosyl)-[2→3(or 2→6)]-O-β-D-galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-O-α-D-mannopyranosyl-(1→3)-O-[O-(N-acetyl-α-neuraminosyl)-[2→3(or 2→6)]-O-β-D-galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-α-D-mannopyranosyl-(1→6)]-O-β-D-mannopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→4)-O-[6-deoxy-α-L-galactopyranosyl-(1→6)]-2-(acetylamino)-2-deoxy-D-glucose. Grade: ≥90%. CAS No. 108341-22-6. Molecular formula: C90H148N6O66. Mole weight: 2370.14. | |
| A2G1 Glycan, 2-AA labelled | A2G1 Glycan, 2-AA labelled is a crucial component in the biomedicine industry used to study glycosylation patterns, which plays a critical role in numerous diseases, including cancer, diabetes, and inflammation. As a fluorescently labelled glycan, it enables researchers to investigate the glycosylation process related to protein-protein and protein-ligand interactions, leading to better understanding and potential therapeutic interventions for these diseases. | |
| A2G1 Glycan, 2-AB labelled | A2G1 Glycan, 2-AB labelled. | |
| A2G1 N-Glycan | A2G1 N-Glycan is a vital component used for studying glycosylation and its impact on diseases such as cancer, autoimmune disorders and neurodegenerative diseases. This glycan plays a crucial role in understanding cellular processes, protein interactions and targeted compound delivery. It aids in the characterization and analysis of glycoproteins. Synonyms: Asialo-, bi-antennary N-linked glycan. | |
| A2 Glycan, 2-AA labelled | A2 Glycan, 2-AA labelled is a vital tool in biomedicine used for studying glycan structures and their involvement in various diseases. It is utilized to analyze glycan compositions and monitor alterations in glycosylation patterns. Synonyms: A2 N-linked oligosaccharide; A2G2S2; G2S2. | |
| A2 Glycan, 2-AB labelled | A2 Glycan, 2-AB labelled. | |
| A2 N-Glycan | A2 N-Glycan is an indispensable biocompatible and bioactive glycobiology compound, aiding in the meticulous analysand comprehensive characterization of glycoproteins. Synonyms: Disialo (2,6), biantennary (A2); A2 glycan; A2G2S2 N-glycan; Di-sialylated, galactosylated, bi-antennary N-linked glycan Mannotriose-di-(N-acetyl-D-glucosamine), bis([N-acetyl-D-neuraminyl]-galactosyl-[N-acetyl-D-glucosaminyl]). Grade: 95%. CAS No. 71496-55-4. Molecular formula: C84H138N6O62. Mole weight: 2224.00. | |
| A3 Glycan | from bovine, ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| A3 Glycan, 2-AA labelled | A3 Glycan, 2-AA labelled, a critical and indispensable instrument in the biomedical sector, is utilized for exploring glycan expression in diverse illnesses, notably cancer and autoimmune disorders. It acts as the ideal substance for glycan analysis and characterization by advanced technologies like mass spectrometry and chromatography. Furthermore, A3 Glycan, 2-AA labelled is crucial for triggering glycomics-related biomarker discovery scientific investigations ensuing precision medication breakthroughs. | |
| A3 Glycan, 2-AB labelled | A3 Glycan, 2-AB labelled. | |
| A3 N-Glycan | A3 N-Glycan is a vital biomolecule commonly found on the surface of many cells. It plays a crucial role in various biological processes, such as cell signaling, immune response, and disease progression. This particular N-glycan is extensively studied in the biomedical industry due to its involvement in numerous diseases, including cancer, autoimmune disorders, and infectious diseases. Synonyms: Trisialylated, galactosylated, triantennary (A3); A3 glycan; A3G3S3 Glycan; (NeuNAc-Gal-GlcNAc)3Man3(GlcNAc)2; Tri-sialylated, galactosylated, tri-antennary N-linked glycan; Mannotriose-di-(N-acetyl-D-glucosamine), tris(sialyl-galactosyl-N-acetyl-D-glucosaminyl; D-Glucose, O-(N-acetyl-α-neuraminosyl)-[2→3(or 2→6)]-O-β-D-galactopyranosyl-(1→4)-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→2)-O-[O. Grade: ≥85%. CAS No. 145164-24-5. Molecular formula: C109H178N8O80. Mole weight: 2880.59. | |
| FA2BG1 Glycan, 2-AA labelled | FA2BG1 Glycan, 2-AA labelled is a biomedical research compound used in glycomics studies. It's particularly useful in the analysis and detection of diseases such as cancer and autoimmune disorders where abnormal glycosylation patterns are often observed. Synonyms: FA2BG1 N-linked oligosaccharide; FA2G1 with bisecting GlcNAc; G1F with bisecting GlcNAc. | |
| FA2BG1 Glycan, 2-AB labelled | FA2BG1 Glycan, 2-AB labelled, a crucial biomolecule with broad implications in the diagnosis and treatment of myriads of cancer types, beckons attention due to its capability as a diagnostic tool to detect alterations in cell surface glycosylation and track cancer treatment's efficacy. Synonyms: FA2BG1 N-linked oligosaccharide, 2-AB labelled; FA2G1 with bisecting GlcNAc, 2-AB labelled; G1F with bisecting GlcNAc, 2-AB labelled. | |
| FA2B Glycan, 2-AA labelled | FA2B Glycan, 2-AA labelled is a prodigious compound, serving as an indispensable instrument for studying and comprehending intricate glycan structures. Renowned and heavily employed in the realm of glycobiology research, this remarkable product unfailingly facilitates an exhaustive exploration of glycosylation processes, as well as an in-depth analysis of the multifaceted interactions between glycans and proteins. | |
| FA2B Glycan, 2-AB labelled | FA2B Glycan, 2-AB labelled. | |
| FA2B N-Glycan | FA2B N-Glycan is a naturally occurring glycan presenting on N-linked glycoproteins. It exhibits pivotal significance in numerous cellular phenomena such as cell adhesion, signaling and immune response. It can be used to study glycosylation patterns and glycan functionality. Synonyms: Asialo, agalacto, core-fucosylated, bisected, bi-antennary N-linked glycan. Mole weight: 1667. | |
| FA2G1 N-Glycan | FA2G1 N-Glycan is a compound assuming a paramount role in the comprehensive exploration and comprehension of glycoproteins alongside their intricate functionalities. With its widespread employment as a research tool, this N-glycan holds the potential for the profound investigation of diverse maladies encompassing cancer, inflammation and hereditary disorders. Synonyms: Asialo, core fucosylated, bi-antennary N-linked glycan; NA2G1F N-Glycan. CAS No. 721918-59-8. Molecular formula: C62H104N4O45. Mole weight: 1625.49. | |
| G1F Glycan, 2-AA labelled | G1F Glycan, 2-AA labelled, a noteworthy carbohydrate molecule, serves as a potent tool for glycomic analysis. Through its ability to detect glycan biomarkers, it has implicated itself as crucial in analyzing aberrant glycosylation patterns in diseases including cancer. This molecular fingerprint finds broad application in mass spectrometry-based glycomic profiling. By furnishing invaluable insights into the progressive role of glycosylation in disease, researchers can harness the potential of this versatile labelled glycan to enhance diagnostic approaches. | |
| G1F Glycan, 2-AB labelled | G1F Glycan, 2-AB labelled. | |
| G2 Glycan | G2 Glycan. Group: Molecular Biology. Grades: Highly Purified. CAS No. 71496-53-2. Pack Sizes: 1mg. Molecular Formula: C62H104N4O46. US Biological Life Sciences. |  Worldwide |
| GNA2 N-Glycan | GNA2 N-Glycan is a resplendent biomedicine used for stduying cancer, inflammatory disorders, and neurodegenerative conditions. Synonyms: Monogalacto, fucosylated, biantennary N-linked glycan. | |
| G-NGA2 N-Glycan | G-NGA2 N-Glycanthe transformative compound engaging in protein modifications. It finds applications in studying glycosylation-related disorders and diseases. Synonyms: Monogalactosylated asialo, biantennary (G-NGA2); Monogalactosylated, asialo, bi-antennary N-linked glycan; Monogalactosylated, asialo, biantennary N-glycan (G-NGA2); O-2-(Acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-2)-O-alpha-D-mannopyranosyl-(1-6)-O-[O-beta-D-galactopyranosyl-(1-4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-2)-alpha-D-mannopyranosyl-(1-3)]-O-beta-D-mannopyranosyl-(1-4)-O-2-(acetylamino)-2-deoxy-beta-D-glucopyranosyl-(1-4)-2-(acetylamino)-2-deoxy-D-glucose. Grade: ≥90%. CAS No. 103584-68-5. Molecular formula: C56H94N4O41. Mole weight: 1479.35. | |
| Hybrid Glycan, 2-AB labelled | Hybrid Glycan, 2-AB labelled. | |
| Hybrid N-Glycan | Hybrid N-Glycan is a crucial element used for researching various diseases such as cancer, genetic disorders and autoimmune diseases. It plays a vital role in understanding the functions and modifications of N-glycosylated proteins. Synonyms: Hybrid-type, bisected, N-linked glycan; M5A1B N-Glycan; Mannopentaose-di-(N-acetylglucosamine), N-acetylglucosaminyl-bisecting-N-acetylglucosaminyl; GlcNAc(GlcNAc)Man5(GlcNAc)2. CAS No. 84182-21-8. Molecular formula: C62H104N4O46. Mole weight: 1641.49. | |
| Lysozyme, Positive Control (LZM, LYZ, Renal Amyloidosis, N-Acetylmuramide Glycanhydrolase, Muramidase) | Lysozyme, Positive Control (LZM, LYZ, Renal Amyloidosis, N-Acetylmuramide Glycanhydrolase, Muramidase). Group: Molecular Biology. Pack Sizes: 15ul. US Biological Life Sciences. | Worldwide |
| MAN-9 Glycan | ?80%. Group: Fluorescence/luminescence spectroscopy. | |
| N-Glycanase (EDTA-Free) from Elizabethkingia meningoseptica, Recombinant | N-Glycanase (EDTA-Free) from Elizabethkingia meningoseptica, Recombinant. Group: Enzymes. Synonyms: N-Glycanase. Purity: The absence of exoglycosidase contaminants was confirmed by extended incubations with the corresponding pNP or MU-glycosides. No protease activity was detectable after incubation of the enzyme with 0.2 mg resorufin-labeled casein for ~18 hours at 37°C according to the method described by Twining. N-Glycanase. Mole weight: ~35 kDa daltons. Activity: > 10 U/mg. Stability: Extended incubations may be performed at 25°C rather than 37°C to promote stability of the N-Glycanase. Storage: Shipped on ice pack for next day delivery. Store enzyme at 2-8°C or -20°C, but avoid repeated freeze-thawing. Form: A sterile-filtered solution in 20 mM Tris-HCl, 50 mM NaCl (pH 7.5). Source: E. coli. Species: Elizabethkingia meningoseptica. N-Glycanase. Cat No: NATE-0483. |  |
| O-Glycanase from Streptococcus pneumoniae, Recombinant | O-Glycanase from Streptococcus pneumoniae, Recombinant. The enzyme is inactivated with sulfhydryl reagents such as p-chloro-mercuribenzene sulfonic acid and transition metals such as mn2+ or zn2+. the enzyme is also inhibited with 1 mm edta. in a highly purified form, o-glycanase adsorbs to glass surfaces and is inactivated or gives variable activities. assays with purified substrates should be carried out in polypropylene vessels, and transfer of the enzyme solutions with glass pipettes should be avoided. the purified enzyme, as formulated, is stable at 2-8°c but about 30% of its activity is lost with a single freeze-thaw cycle. the enzyme activity is not signific...Glycanase. Purity: O-Glycanase is free of contaminating endo-and exoglycosidase activity. No protease activity was detectable after incubation of the enzyme with 0.2 mg resorufin-labeled casein for ~18 hours at 37°C according to the method described by Twining. The production host strain has been extensively tested and does not produce any detectable glycosidases. O-Glycanase. Mole weight: ~180 kDa daltons. Activity: > 12 U/mg. Storage: Shipped on cold pack for next day delivery. Store at 2-8°C. DO NOT FREEZE. Form: A sterile-filtered solution in 20 mM Tris-HCl, 25 mM NaCl (pH 7.5). Source: E. coli. Species: Streptococcus pneumoniae. O-Glycanase. Cat No: NATE-0496. | |
| 1,2,3,4,6-Penta-O-benzoyl-b-D-galactopyranose | 1,2,3,4,6-Penta-O-benzoyl-b-D-galactopyranose is a specific glycosylation agent used in pharmaceutical synthesis processes. It's generally applied in the creation of semi-synthetic antibiotics and a variety of bioactive glycans contributing to treatment research on bacterial infections and immunological diseases. CAS No. 41545-56-6. Molecular formula: C41H32O11. Mole weight: 700.71. | |
| 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-galactopyranose | 1,2,3,4-Tetra-O-acetyl-6-O-(tert-butyldiphenylsilyl)-b-D-galactopyranose, a complex carbohydrate employed in glycans synthesis, displays immense possibilities in treating Alzheimer's, cancer, and autoimmune diseases as suggested by recent biomedical research. Its intricate composition and diversified applicability open doors for extensive explorations on complex carbohydrates' therapeutic potential. Molecular formula: C30H38O10Si. Mole weight: 586.72. | |
| 1,2,3,4-Tetra-O-benzyl-6-O-tert-butyldiphenylsilyl-a-D-mannopyranose | 1,2,3,4-Tetra-O-benzyl-6-O-tert-butyldiphenylsilyl-a-D-mannopyranose, a complex saccharide derivative with a bulky protective structure, is widely employed in biomedicine for its crucial role as a pivotal intermediate in glycosylation processes. Its manifold applications for drug development, specifically in the treatment of pathologies affiliated with impairments in glycan metabolism, make it a highly coveted compound of great promise and potential in pharmacology. Molecular formula: C50H54O6Si. Mole weight: 779.07. | |
| 1,2,3,4-Tetra-O-benzyl-6-O-triisopropylsilyl-b-D-galactopyranose | 1,2,3,4-Tetra-O-benzyl-6-O-triisopropylsilyl-b-D-galactopyranose, a complex carbohydrate compound, is extensively employed in synthetic drug development and drug candidate discovery. This elusive molecule aids in the production of glycan libraries and glycopeptides, facilitating the investigation of carbohydrate-protein interactions implicated in the pathogenesis of malignant neoplasms and viral infections. Molecular formula: C43H56O6Si. Mole weight: 697.01. | |
| 1,2,3,4-Tetra-O-pivaloyl-6-O-(tert-butyldiphenylsilyl)-b-D-galactopyranose | 1,2,3,4-Tetra-O-pivaloyl-6-O-(tert-butyldiphenylsilyl)-b-D-galactopyranose, a structural analogue of galactose, is an essential carbohydrate derivative employed in the synthesis of biologically active glycosylated compounds and pharmaceuticals. Its superior stability and reactivity help in the preparation of diverse glycan mimetics with sustainable and precise protocols. This compound exhibits the potential to serve as a building block in the production of medicinally valuable glycoconjugates, offering an extended range of medicinal applications. CAS No. 1222709-71-8. Molecular formula: C42H62O10Si. Mole weight: 755.04. | |
| 1,2,3,4-Tetra-O-pivaloyl-6-O-trityl-b-D-galactopyranose | 1,2,3,4-Tetra-O-pivaloyl-6-O-trityl-b-D-galactopyranose, a complex chemical compound, acts as a primary precursor for the synthesis of various glycan derivatives. This compound shows immense potential in the biomedical sector, specifically in the development of pharmaceuticals for the targeted treatment of severe diseases like cancer and viral infections. Delving further into the synthesis process can unravel numerous prospects for molecular engineering, carrying the capacity to revolutionize the medicinal industry. Molecular formula: C45H58O10. Mole weight: 758.94. | |
| 1,2,4,6-Tetra-O-benzyl-b-D-galactopyranoside | 1,2,4,6-Tetra-O-benzyl-b-D-galactopyranoside, a pivotal synthetic glycoprotein and glycan structure reagent, has recently been investigated for its potential involvement as a glycosylation inhibitor. Recognized as a promising agent for a myriad of diseases, ranging from cancer to autoimmune disorders, this chemical is at the forefront of research in the field of medicinal chemistry. Molecular formula: C34H36O6. Mole weight: 540.65. | |
| 1,3,4,6-Tetra-O-acetyl-2-O-nonafluorobutane-sulfonyl-b-D-mannopyranose | 1,3,4,6-Tetra-O-acetyl-2-O-nonafluorobutane-sulfonyl-b-D-mannopyranose, an essential intermediary in the production of medicinal substances and biologically active compounds, proves useful for synthesizing possible bactericides and insecticides. This multipurpose compound doubles as a chemoenzymatic synthon in crafting mannosides and glycans, which show promise as therapeutic applications for ailments like cancer and HIV. Its chemical versatility and potential health benefits make this substance an invaluable asset in the pharmaceutical industry. Synonyms: β-D-Mannopyranose, 1,3,4,6-tetraacetate 2-(1,1,2,2,3,3,4,4,4-nonafluoro-1-butanesulfonate). CAS No. 480438-48-0. Molecular formula: C18H19O12SF9. Mole weight: 630.39. | |
| 1,3,4,6-Tetra-O-acetyl-b-D-glucosamine HCl | 1,3,4,6-Tetra-O-acetyl-b-D-glucosamine HCl - a chemical compound known for its numerous therapeutic applications, including the development of drugs for osteoarthritis, rheumatoid arthritis, and autoimmune diseases. Of particular interest is its use in biomedicine, where it has proven invaluable in the preparation of glycan arrays - crucial tools for the study of glycobiology and drug discovery. Its multifaceted properties make it a promising candidate for further research and exploration. Synonyms: 1,3,4,6-Tetra-O-acetyl-2-amino-2-deoxy-b-D-glucopyranose HCl; β-D-Glucopyranose, 2-amino-2-deoxy-, 1,3,4,6-tetraacetate, hydrochloride (1:1); 1,3,4,6-Tetra-O-acetyl-2-amino-2-deoxy-β-D-glucopyranose hydrochloride; 1,3,4,6-Tetra-O-acetyl-β-D-glucosamine hydrochloride; 2-Amino-2-deoxy-1,3,4,6-tetra-O-acetyl-β-D-glucopyranose hydrochloride; NSC 82044; β-D-Glucopyranose 1,3,4,6-tetraacetate-2-amino-2-deoxy hydrochloride. CAS No. 10034-20-5. Molecular formula: C14H21NO9.HCl. Mole weight: 383.78. | |
| 1,3,4,6-Tetra-O-acetyl-N-azidoacetylglucosamine | 1,3,4,6-Tetra-O-acetyl-N-azidoacetylglucosamine, a vital compound employed in biomedical research, serves as an indispensable intermediate. It finds extensive utility in synthesizing glycosylated biomolecules, including glycopeptides and glycoproteins. Possessing an azido functional group, this compound facilitates efficient bioconjugation and labeling investigations. Its versatility stretches to the exploration of cell surface glycans, glycosylation pathways, and glycoengineering. Additionally, it aids in examining cell-surface interactions and potential therapeutic interventions associated with anomalous glycosylation, thereby contributing significantly to the realm of disease management. Synonyms: N-azidoacetylglucosamine-tetraacylated (Ac4GlcNAz); GlcNAz tetraacetate; 1,3,4,6-Tetra-O-acetyl-2-(2-azidoacetamido)-2-deoxy-b-D-glucopyranose; N-Azidoacetylglucosamine tetraacylated; Ac4GlcNAz. Grade: 90%. CAS No. 98924-81-3. Molecular formula: C16H22N4O10. Mole weight: 430.37. | |
| 1,4-β-mannosyl-N-acetylglucosamine phosphorylase | The enzyme isolated from the anaerobic bacterium Bacteroides thetaiotaomicron is involved in the degradation of host-derived N-glycans. Group: Enzymes. Synonyms: BT1033. Enzyme Commission Number: EC 2.4.1.320. 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-2557; 1,4-β-mannosyl-N-acetylglucosamine phosphorylase; EC 2.4.1.320; BT1033. Cat No: EXWM-2557. | |
| 2,3,4,6-Tetra-O-acetyl-5-thio-D-galactopyranosyl trichloroacetimidate | 2,3,4,6-Tetra-O-acetyl-5-thio-D-galactopyranosyl trichloroacetimidate is a vital reagent employed ubiquitously in synthesizing glycopeptides and glycoproteins. Primarily, it is efficacious in assimilating thio-sugars into glycans. Such incorporation may prove valuable in mitigating grievous illnesses like cancer and inflammation. Harnessing its potential correctly can pave the way for numerous scientific advancements. Molecular formula: C16H20Cl3NO9S. Mole weight: 508.76. | |
| 2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl azide | 2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl azide is a biochemical used in biomedical research, especially in the synthesis of glycans for immunological studies. It plays a crucial role in developing drugs for diseases caused by glycan-processing anomalies like Congenital Disorders of Glycosylation. Synonyms: a-D-Mannopyranosyl azide tetraacetate. CAS No. 53784-29-5. Molecular formula: C14H19N3O9. Mole weight: 373.32. | |
| 2,3,4,6-Tetra-O-pivaloyl-b-D-galactopyranosyl isothiocyanate | 2,3,4,6-Tetra-O-pivaloyl-b-D-galactopyranosyl isothiocyanate: A potent biomedical tool used in research for studying cellular interactions. It is commonly employed as a reactive reagent for labeling glycoproteins. With its high affinity for specific proteins, this compound aids in the detection and analysis of glycan-related diseases, contributing to advancements in drug development for targeted therapies. CAS No. 147948-52-5. Molecular formula: C27H43NO9S. Mole weight: 557.70. | |
| 2,3,4-Tri-O-acetyl-6-azido-6-deoxy-a-D-glucopyranosyl trichloroacetimidate | 2,3,4-Tri-O-acetyl-6-azido-6-deoxy-a-D-glucopyranosyl trichloroacetimidate is a highly intricate chemical compound that finds widespread application in the synthesis of glycans and glycoconjugates. This compound, due to its unique structural properties, has garnered immense research interest in the field of glycotherapeutics. With its immense potential in halting the progression of diseases such as cancer, influenza, and HIV, experts are increasingly focusing on the development of glycotherapeutic agents that leverage its sugar modification capabilities. In doing so, there is a hope to enhance immune response and offer better treatment options to patients. CAS No. 191668-79-8. Molecular formula: C14H17Cl3N4O8. Mole weight: 475.67. | |
| 2,3,4-Tri-O-acetyl-6-deoxy-a-D-glucopyranosyl trichloroacetimidate | 2,3,4-Tri-O-acetyl-6-deoxy-a-D-glucopyranosyl trichloroacetimidate is an indispensable compound required for the synthesis of oligosaccharides or glycans. With its widespread application in the biomedical industry, it has been utilized extensively in the development of drugs for a diverse range of diseases encompassing cancer, inflammation, and bacterial infections. This compound has been identified as a vital contributor to the progress in the field of medicine and holds immense potential for future research. Synonyms: (2R,3R,4S,5R,6R)-2-Methyl-6-(2,2,2-trichloro-1-iminoethoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate; SCHEMBL24603577. CAS No. 120449-23-2. Molecular formula: C14H18Cl3NO8. Mole weight: 434.65. | |
| 2,3,4-Tri-O-acetyl-b-L-fucopyranosyl azide | 2,3,4-Tri-O-acetyl-b-L-fucopyranosyl azide, a vital precursor employed in the manufacture of glycans, is indispensable in comprehending and combating ailments like cancer and autoimmune disorders. It is also instituted in chemical glycosylation reactions, culminating in the formation of even more intricate carbohydrates. Emphasising the paramount importance of this intermediate, it delineates the significance of comprehending the complexities of the synthetic processes that culminate in glycan formation. Synonyms: β-L-Galactopyranosyl azide, 6-deoxy-, 2,3,4-triacetate; 2,3,4-Tri-O-acetyl-β-L-fucosyl azide. CAS No. 95581-07-0. Molecular formula: C12H17N3O7. Mole weight: 315.28. | |
| 2,3,4-Tri-O-benzylfucosyllactose | 2,3,4-Tri-O-benzylfucosyllactose is a compound used in biomedical research, specifically in glycan assembly studies. Its applications include the study of anticancer, inflammatory and viral diseases drugs, owing to its unique involvement with cell surface glycan interactions. Molecular formula: C39H50O15. Mole weight: 758.81. | |
| 2'',3'',4''-Tri-O-benzylfucosyllactose | 2'',3'',4''-Tri-O-benzylfucosyllactose, a complex carbohydrate, serves as an invaluable tool for deciphering the intricate interplay between pathogenic bacteria and their host cells. Researchers have extensively explored its potential as a therapeutic agent, particularly in the context of combatting devastating conditions like tuberculosis and pneumonia. In addition, this compound serves as an indispensable reference standard, enabling scientists to precisely investigate the role that fucosylated glycans play in cellular signaling and interactions. Grade: 90%. Molecular formula: C39H50O15. Mole weight: 758.81. | |
| 2,3-O-Isopropylidene-D-ribonolactone | 2,3-O-Isopropylidene-D-ribonolactone is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 30725-00-9. Pack Sizes: 5 g; 10 g. Product ID: HY-76693. |  |
| 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-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-3,4,6-tri-O-acetyl-2-deoxy-D-galactopyranose | 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-D-galactopyranose is a profoundly intricate carbohydrate derivative. As a pivotal intermediary in the fabrication of glycan-centered therapeutic agents and diagnostic components, it showcases unparalleled importance. Leveraging its distinctive molecular composition, this substance assumes a critical function in the research of pharmacological interventions addressing manifold ailments, encompassing cancer, inflammation, and infectious maladies. CAS No. 5132-11-6. Molecular formula: C14H21NO9. Mole weight: 347.32. | |
| 2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl azide | 2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl azide is a glycosyl azide used in the preparation of nonglycosylated androgenic gland hormone (AGH) and glycosylated AGH with N-linked glycan using expressed protein ligation. Synonyms: 2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-beta-D-glucopyranosyl Azide. CAS No. 214467-60-4. Molecular formula: C29H32N4O5. Mole weight: 516.59. | |
| 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-Amino-2-deoxy-D-fucose | 2-Amino-2-deoxy-D-fucose is a highly significant constituent serving as an antecedent in the intricate amalgamation of polysaccharides acknowledged as fucosyl-glycans. These glycans, instrumental in cell identification, immunological retort, and inflammatory processes, assume a paramount status. Synonyms: D-Galactose, 2-amino-2,6-dideoxy-; 2-Amino-2,6-dideoxy-D-galactose; D-Fucose, 2-amino-2-deoxy-; Galactose, 2-amino-2,6-dideoxy-, D-; D-Fucosamine. Grade: ≥95%. CAS No. 6931-59-5. Molecular formula: C6H13NO4. Mole weight: 163.17. | |
| 2-Amino-2-deoxy-L-fucose | 2-Amino-2-deoxy-L-fucose, a monosaccharide of paramount significance, intricately participates in the inherent complexity of glycan biosynthesis. Its versatile attributes serve as a substrate for fucosyltransferases, inducing the production of fucosylated glycans, a heterogeneous group of biomolecules, meticulously regulating critical biological processes, including cell adhesion and signal transduction. Researchers have also investigated its potential therapeutic applications in ameliorating cancer and inflammatory diseases. Synonyms: 2-Amino-2,6-dideoxy-L-galactose; L-Fucosamine. CAS No. 7577-62-0. Molecular formula: C6H13NO4. Mole weight: 163.17. | |
| 2-Aminoacridone | 2-Aminoacridone is a fluorescent label for glycans and saccharides. Group: Biochemicals. Alternative Names: 2-Amino-9(10H)-acridinone; 2-Amino-9-acridone. Grades: Highly Purified. CAS No. 27918-14-5. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C13H10N2O. US Biological Life Sciences. | Worldwide |
| 2-Aminobenzamide | 2-Aminobenzamide is used for efficient fluorescent labelling of glycans and analysis of complex carbohydrates. Group: Biochemicals. Alternative Names: o-Amino-benzamide; 2-Aminobenzamide; 2-Amino Benzene carboxamide; 2-Carbamoylaniline; Anthranilamide; Anthranilimidic acid; NSC 38768; SR 4327; o-Aminobenzamide; o-Carbamoylaniline. Grades: Highly Purified. CAS No. 88-68-6. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
Our database is helping our users find suppliers everyday.
