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 | |
|---|---|---|
| 2-Nitrophenyl-N-acetyl-b-D-glucosaminide 99+% (TLC) | 2-Nitrophenyl-N-acetyl-b-D-glucosaminide 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. |  Worldwide |
| 4-Methylumbelliferyl a-D-glucosaminide | 4-Methylumbelliferyl α-D-glucosaminide is a valuable tool in research for detecting chitinase activity. This substrate can be hydrolyzed by chitinases, enzymes involved in various diseases such as asthma is arthritis is and gastrointestinal disorders. Its fluorescent properties allow for easy detection and quantification, making it ideal for studying chitinase-related diseases and developing potential researchs. Synonyms: 4-Methylumbelliferyl 2-amino-2-deoxy-a-D-glucopyranoside. CAS No. 137687-00-4. Molecular formula: C16H19NO7. Mole weight: 337.32. |  |
| 4-Methylumbelliferyl b-D-glucosaminide | 4-Methylumbelliferyl b-D-glucosaminide's primary function revolves around the identification and quantification of enzymatic activity associated with carbohydrate degradation, specifically glucosaminidase. This compound can use in studying various afflictions stemming from lysosomal storage disorders, encompassing the daunting Gaucher disease and the formidable Tay-Sachs disease. Synonyms: 4-Methylumbelliferyl 2-amino-2-deoxy-b-D-glucopyranoside. CAS No. 58989-36-9. Molecular formula: C16H19NO7. Mole weight: 337.32. | |
| 5-Bromo-4-chloro-3-indolyl-N-acetyl-b-D-glucosaminide 99+% (HPLC) | 5-Bromo-4-chloro-3-indolyl-N-acetyl-b-D-glucosaminide 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| heparan-α-glucosaminide N-acetyltransferase | Brings about the acetylation of glucosamine groups of heparan sulfate and heparin from which the sulfate has been removed. Also acts on heparin. Not identical with EC 2.3.1.3 glucosamine N-acetyltransferase or EC 2.3.1.4 glucosamine-phosphate N-acetyltransferase. Group: Enzymes. Synonyms: acetyl-CoA:α-glucosaminide N-acetyltransferase. Enzyme Commission Number: EC 2.3.1.78. CAS No. 79955-83-2. 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-2258; heparan-α-glucosaminide N-acetyltransferase; EC 2.3.1.78; 79955-83-2; acetyl-CoA:α-glucosaminide N-acetyltransferase. Cat No: EXWM-2258. |  |
| Mannosylglucosaminide | It is produced by the strain of Str. virginiae var. 4243-MTt1. It's an aminoglycoside antibiotic. It has anti-bacterium, mycobacterium and beer yeast effects. Trehalose does not counteract its antibacterial effect against Mycobacterium 607. Synonyms: Mannosyl glucosaminide; Antibiotic 4243; 1-O-(2-Amino-2-deoxy-α-D-gluco-hexopyranosyl)-α-D-manno-hexopyranose; Mannotrehalosamine. CAS No. 14510-04-4. Molecular formula: C12H23NO10. Mole weight: 341.31. | |
| Methyl N-Benzyloxycarbonyl-α-D-glucosaminide | Methyl N-Benzyloxycarbonyl-α-D-glucosaminide is the derivative of D-Glucosamine Hydrochloride (G514950), which is used to prepare medical agent for treating vertigo. Found in chitin, in mucoproteins, and in mucopolysaccharides. Antiarthritic. Recent studies show that its chondroprotective activity is related to its antiapoptic properties. Group: Biochemicals. Grades: Highly Purified. CAS No. 4704-15-8. Pack Sizes: 100mg, 1g. Molecular Formula: C15H21NO7, Molecular Weight: 327.33. US Biological Life Sciences. | Worldwide |
| Methyl N-Benzyloxycarbonyl-α-D-glucosaminide | Methyl N-Benzyloxycarbonyl-α-D-glucosaminide is the derivative of D-Glucosamine Hydrochloride, which is used to prepare medical agent for treating vertigo. Found in chitin, in mucoproteins, and in mucopolysaccharides. Antiarthritic. Recent studies show that its chondroprotective activity is related to its antiapoptic properties. Synonyms: Methyl 2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside; Methyl 2-Deoxy-2-[[(phenylmethoxy)carbonyl]amino]-α-D-glucopyranoside; Methyl 2-(carboxyamino)-2-deoxy-benzyl-ester-α-D-glucopyranoside; Methyl N-Cbz-α-D-glucopyranosaminide. Grades: ≥98%. CAS No. 4704-15-8. Molecular formula: C15H21NO7. Mole weight: 327.33. | |
| Naphthol AS-BI N-acetyl-b-D-glucosaminide | Naphthol AS-BI N-acetyl-b-D-glucosaminide, a compound of utmost significance in biomedical research, emerges as a pivotal factor facilitating the identification and detection of specific ailments and medications. Sporting distinctive attributes, this compound finds extensive usage in a myriad of assays aimed at precisely pinpointing drug-induced liver injury (DILI) and evaluating hepatoxicity stemming from particular pharmaceuticals. Synonyms: Naphthol AS-BI N-acetyl-beta-D-glucosaminide; 3395-37-7; 3-[(2S,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-bromo-N-(2-methoxyphenyl)naphthalene-2-carboxamide; MFCD00076131; Naphthol AS/BI-N-acetyl-beta-D-glucosaminide; Naphthol AS-BI N-acetyl- beta -D-glucosaminide; Naphthol AS-BI 2-acetamido-2-deoxy-beta-D-glucopyranoside; 3-((2S,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-7-bromo-N-(2-methoxyphenyl)-2-naphthamide. CAS No. 3395-37-7. Molecular formula: C26H27BrN2O8. Mole weight: 575.41. | |
| 1-Naphthyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 1-Naphthyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a biomedicine product commonly used as a chemical probe to study the role of glycosidases in diseases like cancer, diabetes, and infectious disorders. Synonyms: 1-Naphthyl N-acetyl-b-D-glucosaminide. CAS No. 10329-98-3. Molecular formula: C18H21NO6. Mole weight: 347.36. | |
| (2-Aminophthalylhydrazido) 2-acetamido-2-deoxy-b-D-glucopyranoside | (2-Aminophthalylhydrazido) 2-acetamido-2-deoxy-b-D-glucopyranoside is a biochemical reagent predominantly used for tagging, visualizing, and distinguishing N-acetyl-β-D-glucosaminyl residues in biomedical studies. It aids in developing diagnostic systems related to pathological conditions with disturbances in N-acetyl-β-D-glucosaminyl residues like Alzheimer's. Synonyms: LUM-NAG; 2-Aminophthalylhydrazido-N-acetyl-b-D-glucosaminide. CAS No. 128879-80-1. Molecular formula: C16H20N4O7. Mole weight: 380.35. | |
| 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. Grades: ≥98% by HPLC. CAS No. 142072-12-6. Molecular formula: C10H18N4O6. Mole weight: 290.27. | |
| 2-Naphthyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 2-Naphthyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a crucial compound utilized in the biomedical industry. It acts as a valuable reagent in the synthesis of various drugs targeting infectious diseases, particularly those caused by Gram-positive bacteria. This product, known for its potent antibacterial properties, plays a vital role in drug research and development. Synonyms: 2-Naphthyl N-acetyl-b-D-glucosaminide. CAS No. 131531-82-3. Molecular formula: C18H21NO6. Mole weight: 347.36. | |
| 4-Methoxyphenyl 6-O-tert-butyldimethylsilyl-2-deoxy-2-(2,2,2-trichloroethoxyformamido)-b-D-glucopyranoside | 4-Methoxyphenyl 6-O-tert-butyldimethylsilyl-2-deoxy-2-(2,2,2-trichloroethoxyformamido)-b-D-glucopyranoside is an intriguing compound wuth remarkable capability to selectively target specific proteins or receptors implicated in diverse pathological processes. Synonyms: 4-Methoxyphenyl 6-O-TBS-N-troc-b-D-glucosaminide. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-a-D-glucopyranoside | 4-Methylumbelliferyl 2-acetamido-2-deoxy-a-D-glucopyranoside, a fluorogenic substrate, is primarily employed in assay development for chitinases and other glycosidases. Its utility lies in its ability to discern the substrate specificities of chitinases, alongside affording a quantitative measurement of chitinase activity. Synonyms: 4-Methylumbelliferyl N-acetyl-a-D-glucosaminide 4MU-a-GlcNAc. CAS No. 80265-04-9. Molecular formula: C18H21NO8. Mole weight: 379.36. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-a-D-glucopyranoside-6-sulfate potassium salt | 4-Methylumbelliferyl 2-acetamido-2-deoxy-a-D-glucopyranoside-6-sulfate potassium salt is an indispensable compound, serving as a pivotal substrate for precise detection and quantification of sulfatase enzyme efficacy. Synonyms: 4MU-a-N-sulpho-D-glucosaminide. CAS No. 154639-35-7. Molecular formula: C18H20KNO11S. Mole weight: 497.52. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-glucopyranoside is an intricate fluorogenic substrate commonly utilized for comprehensive detection of microbial enzymes. Specifically, the substrate facilitates the identification of Escherichia coli and Salmonella Typhimurium through monitoring the hydrolization of N-acetylglucosamine, a vital facet of bacterial cell walls. The advantageous emission of fluorophores when this substrate is cleaved by the aforementioned enzymes reinforces its effectiveness in resistance determination and ailment diagnosis. Synonyms: 4-Methylumbelliferyl N-acetyl-b-D-glucosaminide; 4-MU-GlcNAc; GlcNAc-b-4MU; 2H-1-Benzopyran-2-one, 7-[[2-(acetylamino)-2-deoxy-b-D-glucopyranosyl]oxy]-4-methyl-. Grades: ≥98%. CAS No. 37067-30-4. Molecular formula: C18H21NO8. Mole weight: 379.36. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfate sodium salt | It is a fluorescent substrate for isoenzyme A of N-acetyl-β-D-glucosaminidase (Hexosaminidase A). Synonyms: 4-Methylumbelliferyl N-acetyl-b-D-glucosaminide-6-sulfate sodium salt; 4-Methylumbelliferyl 2-acetamido-2-deoxy-6-sulphate-b-D-glucopyranoside sodium salt; 4MU-b-D-galactoside-6-sulphate sodium salt; 4-Methylumbelliferyl-b-D-galactoside-6-sulphate sodium salt; 7-[[2-(Acetylamino)-2-deoxy-6-O-sulfo-β-D-glucopyranosyl]oxy]-4-methyl-2H-1-benzopyran-2-one Monosodium Salt. Grades: ≥95%. CAS No. 142439-99-4. Molecular formula: C18H20NNaO11S. Mole weight: 481.41. | |
| 4-Nitrophenyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 4-Nitrophenyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a highly esteemed biochemical compound extensively employed in realm of pharmaceutical investigations concerning ailments like cancer, inflammation and bacterial infections. Synonyms: GlcNAc-b-PNP; 4-Nitrophenyl N-acetyl-b-D-glucosamine; PNP-GlcNAc; β-D-Glucopyranoside, 4-nitrophenyl 2-(acetylamino)-2-deoxy-; p-Nitrophenyl 2-Acetamido-2-deoxy-b-D-glucopyranoside; 4-Nitrophenyl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside; Glucopyranoside, p-nitrophenyl 2-acetamido-2-deoxy-, β-D-; β-D-Glucoside, p-nitrophenyl 2-acetamido-2-deoxy-; 4-Nitrophenyl 2-(acetylamino)-2-deoxy-β-D-glucoside; 4-Nitrophenyl N-acetyl-β-D-glucosaminide; 4-Nitrophenyl N-acetylglucosaminide; 4-Nitrophenyl-β-D-2-deoxy-2-N-Acetylglucosaminopyranoside; p-Nitrophenyl 2-acetamido-2-deoxy-β-D-glucopyranoside; p-Nitrophenyl N-acetyl-β-D-glucosaminide; p-Nitrophenyl N-acetyl-β-glucosaminide; p-Nitrophenyl N-acetylglucosaminide. Grades: ≥95%. CAS No. 3459-18-5. Molecular formula: C14H18N2O8. Mole weight: 342.30. | |
| 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a key biochemical recompound used in the detection of β-galactosidase activity. It acts as a chromogenic substrate, producing an intense blue compound upon enzymatic hydrolysis. This compound plays a crucial role in studying gene expression, protein labeling and drug discovery for the research of various diseases, including lysosomal storage disorders and cancers. Synonyms: 5-Bromo-4-chloro-3-indolyl N-acetyl-b-D-glucosaminide; X-GlcNAc; β-D-Glucopyranoside, 5-bromo-4-chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-; 5-Bromo-4-chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside; Indole, 3-[(2-acetamido-2-deoxy-β-D-glucopyranosyl)oxy]-5-bromo-4-chloro-; 5-Bromo-4-chloro-3-indolyl N-acetyl-beta-D-glucosaminide. Grades: ≥95%. CAS No. 4264-82-8. Molecular formula: C16H18BrClN2O6. Mole weight: 449.68. | |
| 6-Bromo-2-naphthyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 6-Bromo-2-naphthyl 2-acetamido-2-deoxy-b-D-glucopyranoside, prominently employed in the biomedical sector, exhibits its indispensable value by facilitating the detection and examination of disease-related proteins, most notably those associated with cancer. Functioning as a substrate for selective enzymes, this compound facilitates the visualization and thorough analysis of aforementioned proteins. Synonyms: 6-Bromo-2-naphthyl N-acetyl-a-D-glucosaminide. CAS No. 212069-27-7. Molecular formula: C18H20BrNO6. Mole weight: 426.26. | |
| 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside | 6-Chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a highly potent and invaluable instrument within the realm of biomedicine, exhibiting its prominence in the context of cellular analysis. With its proficient utility in cell staining, it showcasing a profound ability to monitor and gauge the functionality of β-glucosidases. Additionally, this remarkable compound's inherent capabilities render it conducive to the comprehensive investigation of various afflictions, encompassing lysosomal storage disorders, cancer is and neurological maladies. Synonyms: 6-Chloro-3-indolyl N-acetyl-b-D-glucosaminide Salmon-b-D-GlcNAc 6-Chloro-3-(2-acetamido-2-deoxy-b-D-glucopyranosyloxy)indole. CAS No. 156117-44-1. Molecular formula: C16H19ClN2O6. Mole weight: 370.78. | |
| α-1,3-fucosyltransferase from Helicobacter pylori, Recombinant | A fucosyltransferase is an enzyme that transfers an L-fucose sugar from a GDP-fucose (guanosine diphosphate-fucose) donor substrate to an acceptor substrate. Group: Enzymes. Synonyms: glycoprotein 3-alpha-L-fucosyltransferase; GDP-L-Fuc:N-acetyl-beta-D-glucosaminide alpha1,3-fucosyltransferase; GDP-L-Fuc:Asn-linked GlcNAc alpha1,3-fucosyltransferase; EC 2.4.1.214; Glycoprotein 3-alpha-L-fucosyltransferase. Enzyme Commission Number: EC 2.4.1.214. CAS No. 68247-53-0. Purity: min 95% by SDS-PAGE. α-fucosyltransferase. Source: E. coli. Species: Helicobacter pylori. glycoprotein 3-alpha-L-fucosyltransferase; GDP-L-Fuc:N-acetyl-beta-D-glucosaminide alpha1,3-fucosyltransferase; GDP-L-Fuc:Asn-linked GlcNAc alpha 1,3-fucosyltransferase; EC 2.4.1.214; Glycoprotein 3-alpha-L-fucosyltransferase. Cat No: NATE-1483. | |
| β-N-Acetylglucosaminidase from Streptococcus pneumoniae, Recombinant | Hexosaminidase, sometimes called β-N-acetylhexosaminidase, is reported to liberate terminal β-linked N-acetylglucosamine and N-acetylgalactosamine from a variety of substrates. The activity of β-N-actylglucosaminidase may be determined with the chromogenic substrate p-nitrophenyl-N-acetyl-β-D-glucosaminide. β-N-actylglucosaminidase hydrolyzes the terminal nonreducing N-acetyl-D-hexosamine residues. This enzyme contains two predominant isozymes, Hex A, a heterodimer, and Hex B, a homodimer. N-acetylglucosamine, acetamide, N-2-acetamido-2-deoyglucosylamine, N-acetylnojirimycin, and N-acetyldeoxynojirmycin are known inhibitors. Appli...Commission Number: 3.2.1.52. CAS No. 9012-33-3. β-N-Acetylhexosaminidase. Activity: > 80 units/mg protein. Storage: 2-8°C. Form: buffered aqueous solution, Solution in 20 mM Tris-HCl, pH 7.5, 25 mM NaCl. Source: E. coli. Species: Streptococcus pneumoniae. EC 3.2.1.52; 9012-33-3; hexosaminidase; β-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-acetyl-beta-hexosaminidase; β-hexosaminidase; β-acetylhexosaminidinase; β-D-N-acetylhexosaminidase; β-N-acetyl-D-hexosaminidase; β-N-acetylglucosaminidase; hexosaminidase A; N-acetylhexosaminidase; β-D-hexosaminidase. Pack: vial of > 1.0 unit. Cat No: NATE-0782. | |
| chitinase | Some chitinases also display the activity defined in EC 3.2.1.17 lysozyme. Group: Enzymes. Synonyms: chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. 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-3822; chitinase; EC 3.2.1.14; 9001-06-3; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase. Cat No: EXWM-3822. | |
| Chitinase from Aspergillus niger (food grade) | Chitinase is an extracellular enzyme complex that degrades chitin. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Group: Enzymes. Synonyms: Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. Activity: 200U/g min. Stability: 1 year when properly stored. Storage: STORED HUMIDITY PROTECTED (RH LESS THAN 60) AT TEMPERATURE BELOW 25°C. Form: Light-brown Powder. Source: Aspergillus niger. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: DIS-1010. | |
| Chitinase from Clostridium thermocellum, Recombinant | Chitinase is an extracellular enzyme complex that degrades chitin and has a molecular mass of approximately 30 kDa. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Firstly, chitobiose units are removed from chitin by chitodextrinase-chitinase. The second reaction involves N-acetyl-glucosaminidase-chitobiase, which cleaves the disaccharide to its monomer subunits (that comprise of N-acetyl-D-glucosamine). Group: Enzymes. Synonyms: Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. Purity: > 80 % as judged by SDS-PAGE. Chitinase. Mole weight: 43927.1 Da. Activity: 25 U/mg. Storage: Store at -20°C (shipped at room temperature). Form: Glycerol/buffer solution. Source: Clostridium thermocellum ATCC 27405. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: NATE-1201. | |
| Ethyl 2-acetamido-2-deoxy-b-D-glucopyranoside | Ethyl 2-acetamido-2-deoxy-b-D-glucopyranoside, a pivotal compound in the biomedical field, holds immense significance for numerous applications. With its widespread usage in research and pharmaceutical manufacturing, this compound serves as a fundamental building block for glycosides and glycoconjugates synthesis, facilitating drug discovery efforts. Notably, Ethyl 2-acetamido-2-deoxy-b-D-glucopyranoside also plays a critical role in developing novel therapeutic interventions against bacterial infections, specifically targeting strains like Streptococcus pneumoniae and Haemophilus influenzae. Synonyms: ethyl 2-acetamido-2-deoxy-beta-D-glucopyranoside; Ethyl 2-acetamido-2-deoxy-b-D-glucopyranoside; 1-O-ethyl-N-acetyl-beta-D-glucosamine; ethyl-beta-N-acetylglucosaminide; ethyl beta-N-acetyl-D-glucosaminide; ethyl N-acetyl-beta-D-glucosaminide; N-((2R,3R,4R,5S,6R)-2-Ethoxy-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide; ethyl 2-acetamido-2-deoxy-beta-D-glucoside; CHEBI:62659; ethyl 2-(acetylamino)-2-deoxy-beta-D-glucoside; ethyl 2-(acetylamino)-2-deoxy-beta-D-glucopyranoside; N-[(2R,3R,4R,5S,6R)-2-ethoxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide; Ethyl-beta-D-GlcNAc; Epitope ID:153226; Ethyl-2-acetamido-2-deoxy-b-D-glucopyranoside; Dodecyl-beta-D-galactopyranoside; AKOS002687843; BS-22125; CS-0208313; F74810; A817573; Ethyl 2-(acetylamino)-2-deoxy-|A-D-glucopyranoside; W-202044; Q27132063; beta-D-Glucopyranoside, ethyl 2-(acetylamino)-2-deoxy-. CAS No. 2495-96-7. Molecular formula: C10H19NO6. Mole weight: 249.26. | |
| glycoprotein 3-α-L-fucosyltransferase | Requires Mn2+. The enzyme transfers to N-linked oligosaccharide structures (N-glycans), generally with a specificity for N-glycans with one unsubstituted non-reducing terminal GlcNAc residue. This enzyme catalyses a reaction similar to that of EC 2.4.1.68, glycoprotein 6-α-L-fucosyltransferase, but transferring the L-fucosyl group from GDP-β-L-fucose to form an α1,3-linkage rather than an α1,6-linkage. The N-glycan products of this enzyme are present in plants, insects and some other invertebrates (e.g., Schistosoma, Haemonchus, Lymnaea). Group: Enzymes. Synonyms: GDP-L-Fuc:N-acetyl-β-D-glucosaminide α1,3-fucosyltransferase; GDP-L-Fuc:Asn-linked GlcNAc α1,3-fucosyltransferase; GDP-fucose:β-N-acetylglucosamine (Fuc to (Fucα1?6GlcNAc)-Asn-peptide) α1?3-fucosyltransferase; GDP-L-fucose:glycoprotein (L-fucose to asparagine-. Enzyme Commission Number: EC 2.4.1.214. CAS No. 68247-53-0. α-fucosyltransferase. 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-2442; glycoprotein 3-α-L-fucosyltransferase; EC 2.4.1.214; 68247-53-0; GDP-L-Fuc:N-acetyl-β-D-glucosaminide α1,3-fucosyltransferase; GDP-L-Fuc:Asn-linked GlcNAc α1,3-fucosyltransferase; GDP-fucose:β-N-acetylglucosamin | |
| glycoprotein 6-α-L-fucosyltransferase | This enzyme catalyses a reaction similar to that of EC 2.4.1.214, glycoprotein 3-α-L-fucosyltransferase, but transfers the L-fucosyl group from GDP-β-L-fucose to form an α1,6-linkage rather than an α1,3-linkage. Group: Enzymes. Synonyms: GDP-fucose-glycoprotein fucosyltransferase; GDP-L-Fuc:N-acetyl-β-D-glucosaminide α1?6fucosyltransferase; GDP-L-fucose-glycoprotein fucosyltransferase; glycoprotein fucosyltransferase; guanosine diphosphofucose-glycoprotein fucosyltransferase; GDP-L-fucose:glycoprotein (L-fucose to asparagine-link. Enzyme Commission Number: EC 2.4.1.68. CAS No. 9033-8-3. 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-2611; glycoprotein 6-α-L-fucosyltransferase; EC 2.4.1.68; 9033-08-3; GDP-fucose-glycoprotein fucosyltransferase; GDP-L-Fuc:N-acetyl-β-D-glucosaminide α1?6fucosyltransferase; GDP-L-fucose-glycoprotein fucosyltransferase; glycoprotein fucosyltransferase; guanosine diphosphofucose-glycoprotein fucosyltransferase; GDP-L-fucose:glycoprotein (L-fucose to asparagine-linked N-acetylglucosamine of 4-N-{N-acetyl-β-D-glucosaminyl-(1?2)-α-D-mannosyl-(1?3)-[N-acetyl-β-D-glucosaminyl-(1?2)-α-D-mannosyl-(1?6)]-β-D-mannosyl-(1?4)-N-acetyl-β-D-glucosaminyl- | |
| Hexosaminidase 3A from Thermotoga neapolitana, Recombinant | Hexosaminidase, sometimes called β-N-acetylhexosaminidase, is reported to liberate terminal β-linked N-acetylglucosamine and N-acetylgalactosamine from a variety of substrates. The activity of β-N-actylglucosaminidase may be determined with the chromogenic substrate p-nitrophenyl-N-acetyl-β-D-glucosaminide. β-N-actylglucosaminidase hydrolyzes the terminal nonreducing N-acetyl-D-hexosamine residues. This enzyme contains two predominant isozymes, Hex A, a heterodimer, and Hex B, a homodimer. N-acetylglucosamine, acetamide, N-2-acetamido-2-deoyglucosylamine, N-acetylnojirimycin, and N-acetyldeoxynojirmycin are known inhibitors. Group: Enzyme...weight: 40.6 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Thermotoga neapolitana. EC 3.2.1.52; 9012-33-3; hexosaminidase; β-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-acetyl-beta-hexosaminidase; β-hexosaminidase; β-acetylhexosaminidinase; β-D-N-acetylhexosaminidase; β-N-acetyl-D-hexosaminidase; β-N-acetylglucosaminidase; hexosaminidase A; N-acetylhexosaminidase; β-D-hexosaminidase; Hexosaminidase 3A. Cat No: NATE-1453. | |
| Hexosaminidase 3C from Saccharophagus degradans, Recombinant | Hexosaminidase, sometimes called β-N-acetylhexosaminidase, is reported to liberate terminal β-linked N-acetylglucosamine and N-acetylgalactosamine from a variety of substrates. The activity of β-N-actylglucosaminidase may be determined with the chromogenic substrate p-nitrophenyl-N-acetyl-β-D-glucosaminide. β-N-actylglucosaminidase hydrolyzes the terminal nonreducing N-acetyl-D-hexosamine residues. This enzyme contains two predominant isozymes, Hex A, a heterodimer, and Hex B, a homodimer. N-acetylglucosamine, acetamide, N-2-acetamido-2-deoyglucosylamine, N-acetylnojirimycin, and N-acetyldeoxynojirmycin are known inhibitors. Group: Enzym...ght: 39.5 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: Saccharophagus degradans. EC 3.2.1.52; 9012-33-3; hexosaminidase; β-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-acetyl-beta-hexosaminidase; β-hexosaminidase; β-acetylhexosaminidinase; β-D-N-acetylhexosaminidase; β-N-acetyl-D-hexosaminidase; β-N-acetylglucosaminidase; hexosaminidase A; N-acetylhexosaminidase; β-D-hexosaminidase; Hexosaminidase 3C. Cat No: NATE-1454. | |
| Methyl 2-Acetamido-2-deoxy-β-D-galactopyranoside | Methyl 2-Acetamido-2-deoxy-β-D-galactopyranoside is a compound useful in organic synthesis. Synonyms: Methyl 2-(Acetylamino)-2-deoxy-β-D-glucopyranoside; Methyl N-Acetylglucosaminide; Methyl N-Acetyl-β-D-glucosaminide. Grades: 98%. CAS No. 22256-76-4. Molecular formula: C9H17NO6. Mole weight: 235.23. | |
| Methyl-2-deoxy-2-[[(phenylmethoxy)carbonyl]amino]-4,6-O-(phenylmethylene)-α-D-glucopyranoside | Methyl-2-deoxy-2-[(phenylmethoxy)carbonyl]amino]-4,6-O-(phenylmethylene)-α-D-glucopyranoside, a noteworthy biomedical compound, demonstrates remarkable efficacy in combatting specific diseases. Its substantial impact on inhibiting cancerous cell proliferation renders it an auspicious candidate for targeted therapy against leukemia and breast cancer. Synonyms: Methyl 4,6-O-benzylidene-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside; Methyl 4,6-O-Benzylidene-2-carboxyamino-2-deoxy-benzyl Ester α-D-Glucopyranoside; Methyl 2-[[(benzyloxy)carbonyl]amino]-4-O,6-O-benzylidene-2-deoxy-alpha-D-glucopyranoside; Methyl 4,6-O-benzylidene-N-Cbz-alpha-D-glucosaminide. Grades: ≥95% by HPLC. CAS No. 60076-41-7. Molecular formula: C22H25NO7. Mole weight: 415.44. | |
| Methyl 3-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside | Methyl 3-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside is a pivotal compound in biomedical research, possessing significant relevance as a precursor for the development of glycosylated drugs. Its versatile characteristics foster prospects in studying multifarious afflictions encompassing cancer, bacterial infections and metabolic dysfunctions. Synonyms: Methyl 3-O-benzyl-N-Cbz-alpha-D-glucosaminide; α-D-Glucopyranoside, methyl 2-deoxy-2-[[(phenylmethoxy)carbonyl]amino]-3-O-(phenylmethyl)-. Grades: ≥95%. CAS No. 87907-35-5. Molecular formula: C22H27NO7. Mole weight: 417.46. | |
| N-acetyllactosaminide β-1,6-N-acetylglucosaminyl-transferase | Acts on β-galactosyl-1,4-N-acetylglucosaminyl termini on asialo-α1-acid glycoprotein. Group: Enzymes. Synonyms: N-acetylglucosaminyltransferase; uridine diphosphoacetylglucosamine-acetyllactosaminide β1?6-acetylglucosaminyltransferase; Galβ1?4GlcNAc-R β1?6 N-acetylglucosaminyltransferase; UDP-GlcNAc:Gal-R, β-D-6-N-acetylglucosaminyltransferasel UDP-N-acetyl-D-glucosamine:β-D-galactosyl-1,4-N-acetyl-D-glucosaminide β-1,6-N-acetyl-D-glucosaminyltransferase. Enzyme Commission Number: EC 2.4.1.150. CAS No. 85638-40-0. β-1,3-HexNAc transferase. 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-2377; N-acetyllactosaminide β-1,6-N-acetylglucosaminyl-transferase; EC 2.4.1.150; 85638-40-0; N-acetylglucosaminyltransferase; uridine diphosphoacetylglucosamine-acetyllactosaminide β1?6-acetylglucosaminyltransferase; Galβ1?4GlcNAc-R β1?6 N-acetylglucosaminyltransferase; UDP-GlcNAc:Gal-R, β-D-6-N-acetylglucosaminyltransferasel UDP-N-acetyl-D-glucosamine:β-D-galactosyl-1,4-N-acetyl-D-glucosaminide β-1,6-N-acetyl-D-glucosaminyltransferase. Cat No: EXWM-2377. | |
| Native Bovine β-N-Acetylglucosaminidase | This enzyme, sometimes called β-N-acetylhexosaminidase, is reported to liberate terminal β-linked N-acetylglucosamine and N-acetylgalactosamine from a variety of substrates. The activity of β-N-actylglucosaminidase may be determined with the chromogenic substrate p-nitrophenyl-N-acetyl-β-D-glucosaminide. β-N-actylglucosaminidase hydrolyzes the terminal nonreducing N-acetyl-D-hexosamine residues. This enzyme contains two predominant isozymes, Hex A, a heterodimer, and Hex B, a homodimer. N-acetylglucosamine, acetamide, N-2-acetamido-2-deoyglucosylamine, N-acetylnojirimycin, and N-acetyldeoxynojirmycin are known inhibitors. Applications: Bovine ki...idase A; N-acetylhexosaminidase; β-D-hexosaminidase; 9012-33-3; EC 3.2.1.52. Enzyme Commission Number: EC 3.2.1.52. CAS No. 9012-33-3. β-N-Acetylhexosaminidase. Activity: 10-50 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension. Suspension in 3.2 M (NH4)2SO4, pH approx. 6.0. Source: Bovine kidney. Species: Bovine. hexosaminidase; β-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-acetyl-beta-hexosaminidase; β-hexosaminidase; β-acetylhexosaminidinase; β-D-N-acetylhexosaminidase; β-N-acetyl-D-hexosaminidase; β-N-acetylglucosaminidase; hexosaminidase A; N-acetylhexosaminidase; β-D-hexosaminidase; | |
| Native Canavalia ensiformis β-N-Acetylglucosaminidase | This enzyme, sometimes called β-N-acetylhexosaminidase, is reported to liberate terminal β-linked N-acetylglucosamine and N-acetylgalactosamine from a variety of substrates. The activity of β-N-actylglucosaminidase may be determined with the chromogenic substrate p-nitrophenyl-N-acetyl-β-D-glucosaminide. β-N-actylglucosaminidase hydrolyzes the terminal nonreducing N-acetyl-D-hexosamine residues. This enzyme contains two predominant isozymes, Hex A, a heterodimer, and Hex B, a homodimer. N-acetylglucosamine, acetamide, N-2-acetamido-2-deoyglucosylamine, N-acetylnojirimycin, and N-acetyldeoxynojirmycin are known inhibitors. At ph 4.0, p-nit...ta;-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-acetyl-beta-hexosaminidase; β-hexosaminidase; β-acetylhexosaminidinase; β-D-N-acetylhexosaminidase; β-N-acetyl-D-hexosaminidase; β-N-acetylglucosaminidase; hexosaminidase A; N-acetylhexosaminidase; β-D-hexosaminidase; EC 3.2.1.52; 9012-33-3. Enzyme Commission Number: EC 3.2.1.52. CAS No. 9012-33-3. β-N-Acetylhexosaminidase. Activity: > 15 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension. Suspension in 2.5 M (NH4)2SO4, pH 7.0. Source: Canavalia ensiformis. hexosaminidase; β-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-ac | |
| Native Human β-N-Acetylglucosaminidase | This enzyme, sometimes called β-N-acetylhexosaminidase, is reported to liberate terminal β-linked N-acetylglucosamine and N-acetylgalactosamine from a variety of substrates. The activity of β-N-actylglucosaminidase may be determined with the chromogenic substrate p-nitrophenyl-N-acetyl-β-D-glucosaminide. β-N-actylglucosaminidase hydrolyzes the terminal nonreducing N-acetyl-D-hexosamine residues. This enzyme contains two predominant isozymes, Hex A, a heterodimer, and Hex B, a homodimer. N-acetylglucosamine, acetamide, N-2-acetamido-2-deoyglucosylamine, N-acetylnojirimycin, and N-acetyldeoxynojirmycin are known inhibitors. Applications: Β-n-...etylhexosaminidase; β-D-hexosaminidase; 9012-33-3; EC 3.2.1.52. Enzyme Commission Number: EC 3.2.1.52. CAS No. 9012-33-3. β-N-Acetylhexosaminidase. Activity: 6-20 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension. Suspension in 2.4 M (NH4)2SO4 containing 0.15 M NaCl and 0.1 M sodium phosphate, pH 6.0. Source: Human placenta. Species: Human. hexosaminidase; β-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-acetyl-beta-hexosaminidase; β-hexosaminidase; β-acetylhexosaminidinase; β-D-N-acetylhexosaminidase; β-N-acetyl-D-hexosaminidase; β-N-acetylglucosaminidase; hexosaminidase A; N-acetylhexosaminidase | |
| Native Jack Bean β-(1-2,3,4,6) Hexosaminidase, Sequencing-grade | Hexosaminidase, sometimes called β-N-acetylhexosaminidase, is reported to liberate terminal β-linked N-acetylglucosamine and N-acetylgalactosamine from a variety of substrates. The activity of β-N-actylglucosaminidase may be determined with the chromogenic substrate p-nitrophenyl-N-acetyl-β-D-glucosaminide. β-N-actylglucosaminidase hydrolyzes the terminal nonreducing N-acetyl-D-hexosamine residues. This enzyme contains two predominant isozymes, Hex A, a heterodimer, and Hex B, a homodimer. N-acetylglucosamine, acetamide, N-2-acetamido-2-deoyglucosylamine, N-acetylnojirimycin, and N-acetyldeoxynojirmycin are known inhibitors. Group: Enzymes. Synonyms: β-(1-2,3,4,6) Hexosaminidase; hexosaminidase; β-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-acetyl-beta-hexosaminidase; β-hexosaminidase; β-acetylhexosaminidinase; β-D-N-acetylhe. Hexosaminidase. Source: Jack Bean. β-(1-2,3,4,6) Hexosaminidase; hexosaminidase; β-acetylaminodeoxyhexosidase; N-acetyl-β-D-hexosaminidase; N-acetyl-beta-hexosaminidase; β-hexosaminidase; β-acetylhexosaminidinase; β-D-N-acetylhexosaminidase; β-N-acetyl-D-hexosaminidase; β-N-acetylglucosaminidase; hexosaminidase A; N-acetylhexosaminidase; β-D-hexosaminidase. Cat No: NATE-0343. | |
| Native Streptomyces griseus Chitinase | Chitinase is an extracellular enzyme complex that degrades chitin and has a molecular mass of approximately 30 kDa. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Firstly, chitobiose units are removed from chitin by chitodextrinase-chitinase. The second reaction involves N-acetyl-glucosaminidase-chitobiase, which cleaves the disaccharide to its monomer subunits (that comprise of N-acetyl-D-glucosamine). Applications: Chitinase from streptomyces griseus has been used to study the effect of the allosamidin on the regulatory system for chitinase production. it has also been used to study the enrichment of chitinolytic microorganisms. this enrichment wa...;-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. Activity: > 200 units/g solid. Storage: -20°C. Form: lyophilized powder (essentially salt free). Source: Streptomyces griseus. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: NATE-0123. | |
| Native Trichoderma viride Chitinase | Chitinase is an extracellular enzyme complex that degrades chitin and has a molecular mass of approximately 30 kDa. Chitin is degraded to N-acetyl-D-glucosamine in 2 enzymatic reactions. Firstly, chitobiose units are removed from chitin by chitodextrinase-chitinase. The second reaction involves N-acetyl-glucosaminidase-chitobiase, which cleaves the disaccharide to its monomer subunits (that comprise of N-acetyl-D-glucosamine). Applications: Chitinase from trichoderma viride has been used in a study to investigate the differential release of high mannose structural isoforms by fungal and bacterial endo-β-n-acetylglucosaminidases. chitinase from trichoderma viride has al...glucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Enzyme Commission Number: EC 3.2.1.14. CAS No. 9001-6-3. Chitinase. Activity: > 600 units/g solid. Storage: -20°C. Form: lyophilized powder. Source: Trichoderma viride. Chitinase; chitodextrinase; 1,4-β-poly-N-acetylglucosaminidase; poly-β-glucosaminidase; β-1,4-poly-N-acetyl glucosamidinase; poly[1,4-(N-acetyl-β-D-glucosaminide)] glycanohydrolase; (1->4)-2-acetamido-2-deoxy-beta-D-glucan glycanohydrolase; EC 3.2.1.14. Cat No: NATE-0124. | |
| Phenyl 2-acetamido-2-deoxy-a-D-glucopyranoside | Phenyl 2-acetamido-2-deoxy-a-D-glucopyranoside is a compound product with potential antiviral and antimicrobial properties, finding applications in drug development targeted towards viral and bacterial infections. Synonyms: 1-Phenyl-2-acetamido-2-deoxy-a-D-glucoside; Phenyl N-acetyl-a-D-glucosamine; b-Phenyl-n-acetyl-a-D-glucosaminide. CAS No. 10139-04-5. Molecular formula: C14H19NO6. Mole weight: 297.3. | |
| Phenyl 2-acetamido-2-deoxy-b-D-glucopyranoside | Phenyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a versatile compound widely used in the biomedical industry. It serves as a crucial component in the synthesis of various drugs and therapies aimed at treating diseases such as bacterial infections, inflammation, and cancer. This compound exhibits potent biological activities that make it an indispensable tool in biomedical research and drug development. Synonyms: Phenyl 2-acetamido-2-deoxy-beta-D-glucopyranoside; PHENYL-N-ACETYL-BETA-D-GLUCOSAMINIDE; Phenyl 2-acetamido-2-deoxy-b-D-glucopyranoside; PHENYL N-ACETYL-BETA-D-GLUCOSAMINIDE; phenyl beta-N-acetyl-D-glucosaminide; phenyl 2-acetamido-2-deoxy-beta-D-glucoside; CHEBI:61632; N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-phenoxyoxan-3-yl]acetamide; D-Glucosaminide A; N-((2S,3R,4R,5S,6R)-4,5-Dihydroxy-6-(hydroxymethyl)-2-phenoxytetrahydro-2H-pyran-3-yl)acetamide; EINECS 226-946-6; Epitope ID:141117; SCHEMBL11786108; DTXSID40204287; AKOS002688201; Phenyl N-acetyl-beta-D-glucosaminide, >=98%; Phenyl 2-acetamido-2-deoxy-beta-D-glucopyranoside?; W-203109; Q27131217. CAS No. 5574-80-1. Molecular formula: C14H19NO6. Mole weight: 297.3. | |
| Resorufin N-acetyl-b-D-glucosamine | Resorufin N-acetyl-b-D-glucosamine is a powerful biomedical tool, playing a crucial role in deciphering and studying multifarious enzymatic responses across diverse pathological conditions. With innate fluorogenic properties, it proficiently serves as a versatile substrate for key enzymes encompassing glucosaminidases, chitinases and glycosidases. Synonyms: Resorufinyl 2-acetamido-2-deoxy-beta-D-glucopyranoside; N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(7-oxophenoxazin-3-yl)oxyoxan-3-yl]acetamide; Resorufin-beta-D-glucosaminide; RNAG [Resorufin N-acetyl-beta-D-glucosamine];7-[[2-(Acetylamino)-2-deoxy-|A-D-glucopyranosyl]oxy]-3H-phenoxazin-3-one. CAS No. 124762-32-9. Molecular formula: C20H20N2O8. Mole weight: 416.38. | |
| 2-Acetamido-1,2-dideoxynojirimycin | An analogue of deoxynojirimycin, was found to be a potent inhibitor of a number of N-acetyl glucosaminidases. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 2-Acetamido-1,2-dideoxynojirimycin Hydrochloride | 2-Acetamido-1,2-dideoxynojirimycin is an analogue of deoxynojirimycin, was found to be a potent inhibitor of a number of N-acetyl glucosaminidases. Group: Biochemicals. Grades: Highly Purified. CAS No. 1356848-49-1. Pack Sizes: 500ug, 1mg. Molecular Formula: C8H17ClN2O4. US Biological Life Sciences. | Worldwide |
| 4-Methylumbelliferyl 2-Acetamido-2-deoxy-b-D-glucopyranoside 6-Sulphate Sodium Salt | 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-glucopyranoside 6-sulphate sodium salt is a fluorescent substrate for isoenzyme A of N-acetyl- β-D-glucosaminidase (Hexosaminidase A). It can also be used in biological study of characterization of the mutant β-subunit of β-hexosaminidase for dimer formation responsible for the adult form of Sandhoff disease with the motor neuron disease phenotype. Group: Biochemicals. Grades: Highly Purified. CAS No. 142439-99-4. Pack Sizes: 5mg, 10mg. Molecular Formula: C18H21NO11S; Na, Molecular Weight: 459.422299. US Biological Life Sciences. | Worldwide |
| 4-Methylumbelliferyl 2-sulfamino-2-deoxy-α-D-Glucopyranoside sodium salt | 4-Methylumbelliferyl 2-sulfamino-2-deoxy-α-D-Glucopyranoside (4-MU-α-GlcNS) is a fluorogenic substrate for heparin sulphamidase. 4-MU-α-GlcNS is cleaved by heparin sulphamidase to yield 4-MU-α-GlcNH2, which is then cleaved by α-glucosaminidase to release the fluorescent moiety 4-MU. 4-MU-α-GlcNS has been used to quantify heparin sulphamidase deficiencies associated with Mucopolisaccaridosis IIIA and other lysosomal disorders. Synonyms: 4-MU-α-GlcNS; 7-[[2-deoxy-2-(sulfoamino)-α-D-glucopyranosyl]oxy]-4-methyl-2H-1-benzopyran-2-one monosodium salt. Grades: ≥98%. CAS No. 460085-45-4. Molecular formula: C16H18NNaO10S. Mole weight: 439.4. | |
| 6-Chloro-3-indolyl-ß-D-galactopyranoside | magenta b-galactosidase substrate. N-acetyl b-D-glucosaminidase substrate. Product ID: 9-00613. |  |
| α-N-acetylglucosaminidase | Hydrolyses UDP-N-acetylglucosamine. Group: Enzymes. Synonyms: α-acetylglucosaminidase; N-acetyl-α-D-glucosaminidase; N-acetyl-α-glucosaminidase; α-D-2-acetamido-2-deoxyglucosidase. Enzyme Commission Number: EC 3.2.1.50. CAS No. 37288-40-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3913; α-N-acetylglucosaminidase; EC 3.2.1.50; 37288-40-7; α-acetylglucosaminidase; N-acetyl-α-D-glucosaminidase; N-acetyl-α-glucosaminidase; α-D-2-acetamido-2-deoxyglucosidase. Cat No: EXWM-3913. | |
| APA-1 | 1-Azidiridinepropanoic acid, 2-{[3-(1-Azidiridinyl)-1-oxopropoxy]methyl}-2-(hydroxymethyl)-1,3-propanediyl ester. Inhibits N-acetyl-b-D -glucosaminidase. CAS No. 57116-45-7. Product ID: 9-01616. Purity: aziridine content 6.0-7.0 meq/g, aziridine functionality ~2.8. | |
| β-Acetylglucosaminidase 18A from Bacteroides thetaiotaomicron, Recombinant | β-acetylglucosaminidase 18A, is an enzyme from Bacteroides thetaiotaomicron that participates in the endohydrolysis of the diacetylchitobiosyl unit in high-mannose glycopeptides and glycoproteins containing the (Man(GlcNAc)(2))Asn-structure. One N-acetyl-D-glucosamine residue remains attached to the protein; the rest of the oligosaccharide is released intact. Recombinant BtAcp18A (GH18), purified from Escherichia coli, is a single domain family 18 Glycoside Hydrolase (GH18). Group: Enzymes. Synonyms: beta-N-acetyl-D-hexosaminide; N-acetylhexosaminohydrolase; β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. Enzyme Commission Number: EC 3.2.1.96. CAS No. 37278-88-9. Purity: >50% by SDS-PAGE. β-N-Acetylhexosaminidase. Mole weight: 50.3 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. beta-N-acetyl-D-hexosaminide; N-acetylhexosaminohydrolase; β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. Cat No: NATE-1291. | |
| β-acetylglucosaminidase 73A from Clostridium perfringens, Recombinant | This enzyme releases non-reducing terminal β1-2, β1-3, β1-4 and β1-6 linked N-acetylglucosamine from complex carbohydrates. When incubated with oligosaccharides at low concentrations (<50 mU/ml) the enzyme can differentiate between GlcNAcβ1-2Man, GlcNAcβ1-4Man and GlcNAcβ1-6Man linkages. Under such conditions, the enzyme cleaves essentially only β1-2 linked GlcNAc, with two provisos. Firstly, β1-2 GlcNAc is not hydrolyzed if the mannose to which it is substituted has a substitution at C-6. Thus, the enzyme is useful for the analysis of tri-antennary oligosaccharides. Secondly, if the β-linked mannose of th...etylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. Purity:>90% by SDS-PAGE. β-N-Acetylhexosaminidase. Mole weight: 24.6 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium perfringens. beta-N-acetyl-D-hexosaminide; N-acetylhexosaminohydrolase; β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase; β-Acetylhexosaminidase; β-acetylglucosaminidase 73A. Cat No: NATE-1289. | |
| β-acetylglucosaminidase 73A from Lactococcus lactis, Recombinant | This enzyme releases non-reducing terminal β1-2, β1-3, β1-4 and β1-6 linked N-acetylglucosamine from complex carbohydrates. When incubated with oligosaccharides at low concentrations (<50 mU/ml) the enzyme can differentiate between GlcNAcβ1-2Man, GlcNAcβ1-4Man and GlcNAcβ1-6Man linkages. Under such conditions, the enzyme cleaves essentially only β1-2 linked GlcNAc, with two provisos. Firstly, β1-2 GlcNAc is not hydrolyzed if the mannose to which it is substituted has a substitution at C-6. Thus, the enzyme is useful for the analysis of tri-antennary oligosaccharides. Secondly, if the β-linked mannose of the ...ta;-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. Purity:>90% by SDS-PAGE. β-N-Acetylhexosaminidase. Mole weight: 19.4 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: Lactococcus lactis. beta-N-acetyl-D-hexosaminide; N-acetylhexosaminohydrolase; β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase; β-Acetylhexosaminidase; β-acetylglucosaminidase 73A. Cat No: NATE-1290. | |
| β-N-Acetylhexosaminidase from Streptococcus pneumoniae, Recombinant | This enzyme releases non-reducing terminal β1-2, β1-3, β1-4 and β1-6 linked N-acetylglucosamine from complex carbohydrates. When incubated with oligosaccharides at low concentrations (<50 mU/ml) the enzyme can differentiate between GlcNAcβ1-2Man, GlcNAcβ1-4Man and GlcNAcβ1-6Man linkages. Under such conditions, the enzyme cleaves essentially only β1-2 linked GlcNAc, with two provisos. Firstly, β1-2 GlcNAc is not hydrolyzed if the mannose to which it is substituted has a substitution at C-6. Thus, the enzyme is useful for the analysis of tri-antennary oligosaccharides. Secondly, if the β-linked mannose of the conserved pentasaccharide core is substituted with a "bisecting" GlcNAc then only the β1-2 linked GlcNAc linked to mannose on the α1-3 arm is cleaved. At higher concentrations of the enzyme, β1-4 and β1-6 linked GlcNAc may also be hydrolyzed. Group: Enzymes. Synonyms: β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. β-N-Acetylhexosaminidase. Source: E. coli. Species: Streptococcus pneumoniae. β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. Cat No: NATE-0784. | |
| β-N-Acetylhexosaminidase from Streptococcus pyogenes, Recombinant | This enzyme releases non-reducing terminal β1-2, β1-3, β1-4 and β1-6 linked N-acetylglucosamine from complex carbohydrates. When incubated with oligosaccharides at low concentrations (<50 mU/ml) the enzyme can differentiate between GlcNAcβ1-2Man, GlcNAcβ1-4Man and GlcNAcβ1-6Man linkages. Under such conditions, the enzyme cleaves essentially only β1-2 linked GlcNAc, with two provisos. Firstly, β1-2 GlcNAc is not hydrolyzed if the mannose to which it is substituted has a substitution at C-6. Thus, the enzyme is useful for the analysis of tri-antennary oligosaccharides. Secondly, if the β-linked mannose of the ...ay also be hydrolyzed. Group: Enzymes. Synonyms: beta-N-acetyl-D-hexosaminide; N-acetylhexosaminohydrolase; β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. Enzyme Commission Number: EC 3.2.1.52. CAS No. 9012-33-3. Purity:> 95 % as judged by SDS-PAGE. β-N-Acetylhexosaminidase. Mole weight: 67487.4 Da. Activity: 5.56 U/mg. Storage: Store at -20°C. Form: Supplied as a freeze-dried powder. Source: Streptococcus pyogenes M1 GAS SF370. beta-N-acetyl-D-hexosaminide; N-acetylhexosaminohydrolase; β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. Cat No: NATE-1220. | |
| β-N-Acetylhexosaminidase from Xanthomonas manihotis, Recombinant | This enzyme releases non-reducing terminal β1-2, β1-3, β1-4 and β1-6 linked N-acetylglucosamine from complex carbohydrates. When incubated with oligosaccharides at low concentrations (<50 mU/ml) the enzyme can differentiate between GlcNAcβ1-2Man, GlcNAcβ1-4Man and GlcNAcβ1-6Man linkages. Under such conditions, the enzyme cleaves essentially only β1-2 linked GlcNAc, with two provisos. Firstly, β1-2 GlcNAc is not hydrolyzed if the mannose to which it is substituted has a substitution at C-6. Thus, the enzyme is useful for the analysis of tri-antennary oligosaccharides. Secondly, if the β-linked mannose of the ...cing β-n-acetylglucosamine residues from oligosaccharides. Applications: Biosynthesis of glycans in eukaryotes, glycoprotein production in various expression systems, protein digestion, removal of n-linked & o-linked glycans from glycoproteins, sequencing glycans. Group: Enzymes. Synonyms: β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. β-N-Acetylhexosaminidase. Mole weight: 71000 daltons. Storage: 4°C, Avoid repeated freeze/thaw cycles. Source: E.coli. Species: Xanthomonas manihotis. β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. Cat No: NATE-0934. | |
| Chrysin | blue-green b-galactoside substrate. N-acetyl a-D-glucosaminidase substrate. CAS No. 480-40-0. Product ID: 9-00614. Molecular formula: C15H10O4. Mole weight: 254.24. Purity: dye 50-100 mm/g. | |
| Endoglycosidase H from Streptomyces plicatus, Recombinant | The enzyme Endoglycosidase H is an enzyme with system name glycopeptide-D-mannosyl-N4-(N-acetyl-D-glucosaminyl)2-asparagine 1,4-N-acetyl-beta-glucosaminohydrolase. It is a highly specific endoglycosidase which cleaves asparagine-linked mannose rich oligosaccharides, but not highly processed complex oligosaccharides from glycoproteins. It is used for research purposes to deglycosylate glycoproteins. Group: Enzymes. Synonyms: EC 3.2.1.96;. Enzyme Commission Number: EC 3.2.1.96. CAS No. 37278-88-9. Endo-β-N-acetylglucosaminidase. Storage: 2-8°C. Form: Type I, buffered aqueous solution, Solution in 0.05 M sodium phosphate, pH 7, containing 25 mM EDTA and preservative; Type II, buffered aqueous solution, Solution in 20 mM Tris HCl, pH 7.5, containing 50 mM NaCl, 1 mM EDTA. Source: E. coli. Species: Streptomyces plicatus. EC 3.2.1.96; Endo H; β-N-Acetylglucosaminidase H; N,N'-diacetylchitobiosyl β-N-acetylglucosaminidase; endo-β-N-acetylglucosaminidase; mannosyl-glycoprotein endo-β-N-acetylglucosamidase; di-N-acetylchitobiosyl β-N-acetylglucosaminidase; endo-β-acetylglucosaminidase; endo-β-(14)-N-acetylglucosaminidase; mannosyl-glycoprotein 1,4-N-acetamidodeoxy-β-D-glycohydrolase; endoglycosidase S; endo-N-acetyl-β-D-glucosaminidase; endo-N-acetyl-β-glucosaminidase; endo-&b | |
| exo-1,4-β-D-glucosaminidase | Chitosan is a partially or totally N-deacetylated chitin derivative that is found in the cell walls of some phytopathogenic fungi and comprises D-glucosamine residues with a variable content of GlcNAc residues. Acts specifically on chitooligosaccharides and chitosan, having maximal activity on chitotetraose, chitopentaose and their corresponding alcohols. The enzyme can degrade GlcN-GlcNAc but not GlcNAc-GlcNAc. A member of the glycoside hydrolase family 2 (GH-2). Group: Enzymes. Synonyms: CsxA; GlcNase; exochitosanase; GlmA; exo-β-D-glucosaminidase; chitosan exo-1,4-β-D-glucosaminidase. Enzyme Commission Number: EC 3.2.1.165. 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-3847; exo-1,4-β-D-glucosaminidase; EC 3.2.1.165; CsxA; GlcNase; exochitosanase; GlmA; exo-β-D-glucosaminidase; chitosan exo-1,4-β-D-glucosaminidase. Cat No: EXWM-3847. | |
| Keratanase II from Bacillus circulans, Recombinant | Keratansae II hydrolyzes 1, 3-beta-glucosaminidic linkages to galactose in keratan sulfate. On cleavage, the enzyme requires the sulfate at 6-0 position of the participating glucosamine, but acts independently of the sulfate at 6-0 position of the galactose linked to the glucosamine. Applications: Used in the screening and diagnosis of morquio a syndrome (mps iva). validation of an lc-ms/ms assay for detecting relevant disaccharides from keratan sulfate as a biomarker for morquio a syndrome. Group: Enzymes. Purity: >90%. Endo-β-galactosidase. Storage: Reconstituted protein can be stored at 4°C or in small aliquots at -20°C or below. Avoid repeated freeze-thaw cycles. Form: Powder. Source: E. coli. Species: Bacillus circulans. Endo-β-galactosidase; endo-β-galactosidase; keratan sulfate endogalactosidase; keratanase; keratan-sulfate 1,4-β-D-galactanohydrolase; Keratanase II. Cat No: NATE-1618. | |
| mannosyl-glycoprotein endo-β-N-acetylglucosaminidase | A group of related enzymes. Group: Enzymes. Synonyms: N,N'-diacetylchitobiosyl β-N-acetylglucosaminidase; endo-β-N-acetylglucosaminidase; mannosyl-glycoprotein endo-β-N-acetylglucosamidase; di-N-acetylchitobiosyl β-N-acetylglucosaminidase; endo-β. Enzyme Commission Number: EC 3.2.1.96. CAS No. 37278-88-9. Endo-β-N-acetylglucosaminidase. 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-3959; mannosyl-glycoprotein endo-β-N-acetylglucosaminidase; EC 3.2.1.96; 37278-88-9; N,N'-diacetylchitobiosyl β-N-acetylglucosaminidase; endo-β-N-acetylglucosaminidase; mannosyl-glycoprotein endo-β-N-acetylglucosamidase; di-N-acetylchitobiosyl β-N-acetylglucosaminidase; endo-β-acetylglucosaminidase; endo-β-(1?4)-N-acetylglucosaminidase; mannosyl-glycoprotein 1,4-N-acetamidodeoxy-β-D-glycohydrolase; endoglycosidase S; endo-N-acetyl-β-D-glucosaminidase; endo-N-acetyl-β-glucosaminidase; endo-β-N-acetylglucosaminidase D; endo-β-N-acetylglucosaminidase F; endo-β-N-acetylglucosaminidase H; endo-β-N-acetylglucosaminidase L; glycopeptide-D-mannosyl-4-N-(N-acetyl-D-glucosaminyl)2-asparagine 1,4-N-acetyl-β-glucosaminohydrolase; endoglycosidase H. Cat No: EXWM-3959. | |
| N4-(β-N-acetylglucosaminyl)-L-asparaginase | Acts only on asparagine-oligosaccharides containing one amino acid, i.e., the asparagine has free α-amino and α-carboxyl groups [cf. EC 3.5.1.52, peptide-N4-(N-acetyl-β-glucosaminyl)asparagine amidase]. Group: Enzymes. Synonyms: aspartylglucosylamine deaspartylase; aspartylglucosylaminase; aspartylglucosaminidase; aspartylglycosylamine amidohydrolase; N-aspartyl-β-glucosaminidase; glucosylamidase; β-aspartylglucosylamine amidohydrolase; 4-N-(β-N-acetyl-D-glucosaminyl)-L-asparagine amidohydrolase. Enzyme Commission Number: EC 3.5.1.26. CAS No. 9075-24-5. 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-4416; N4-(β-N-acetylglucosaminyl)-L-asparaginase; EC 3.5.1.26; 9075-24-5; aspartylglucosylamine deaspartylase; aspartylglucosylaminase; aspartylglucosaminidase; aspartylglycosylamine amidohydrolase; N-aspartyl-β-glucosaminidase; glucosylamidase; β-aspartylglucosylamine amidohydrolase; 4-N-(β-N-acetyl-D-glucosaminyl)-L-asparagine amidohydrolase. Cat No: EXWM-4416. | |
| Native Jack bean β-N-Acetylhexosaminidase | The enzyme exhibits a broad specificity, cleaving non-reducing terminal β (1-2,3,4,6)-linked N-acetylglucosamine (GlcNAc) and N-acetylgalactosamine (GalNAc) residues. This enzyme is very useful in the study of isolated glycans, glycolipids and glycoproteins, especially in combination with β-N-acetylhexosaminidase from S. pneumoniae. Group: Enzymes. Synonyms: β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. β-N-Acetylhexosaminidase. Source: Jack bean. β-N-Acetylhexosaminidase; N-Acetyl-β-D-glucosaminidase, β-N-Acetylglucosaminidase. Cat No: NATE-0783. | |
| Native Streptomyces fulvissimus TU-6 Labiase | Labiase from Streptomyces fulvissimus is an enzyme preparation useful for the lysis of many Gram-positive bacteria such as Lactobacillus, Aerococcus and, Streptococcus. Labiase contains β-N-acetyl-D-glucosaminidase and lysozyme activity. Applications: Labiase from streptomyces fulvissimus is an enzyme preparation useful for the lysis of many gram-positive bacteria such as lactobacillus, aerococcus and, streptococcus. labiase contains β-n-acetyl-d-glucosaminidase and lysozyme activity. ph optimum for activity: ph ~4 ph optimum for stability: ph 4-8. Group: Enzymes. Synonyms: Labiase. Labiase. Activity: > 10.0 units/g solid. Storage: 2-8°C. Source: Streptomyces fulvissimus TU-6. Labiase. Cat No: NATE-0369. | |
| Streptozotocin | Antibiotic Diabetogenic. Diabetes inducer. Induces diabetes mellitus in animal models through its toxic effects on pancreatic beta-cells Mutagenic. Potent alkylating agent. Potent DNA methylating agent Nitric oxide (NO) donor. Vasorelaxant. Cytotoxic to cells that express GLUT2 glucose transporter. O-GlcNAc-selective N-acetyl-beta-D-glucosaminidase (O-GlcNAcase) inhibitor. Genotoxic. Induces DNA damage. Produces DNA strand breaks. Cell death inducer. Antineoplastic. Anti-cancer agent used in chemotherapy. Induces cell cylce arrest at G2. Group: Biochemicals. Alternative Names: 2-Deoxy-2-[[ (methylnitrosoamino) carbonyl]amino]-D-glucose; D-2-Deoxy-2- (3-methyl-3-nitrosoureido) glucopyranose; Estreptozocin; NSC 37917; NSC 85998; STRZ; STZ; Streptozocin; Streptozoticin; U 9889; Zanosar. Grades: Highly Purified. CAS No. 18883-66-4. Pack Sizes: 50mg, 250mg, 1g. Molecular Formula: C?H??N?O?. US Biological Life Sciences. | Worldwide |
Our database is helping our users find suppliers everyday.
