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| Product | Description | |
|---|---|---|
| 1,3,4,6-Tetra-O-acetyl-N-propanoyl-D-mannosamine | 1,3,4,6-Tetra-O-acetyl-N-propanoyl-D-mannosamine is a key compound used in biomedicine for the synthesis of potential antiviral drugs. It possesses significant activity against various viral diseases by inhibiting viral replication or entry into host cells. Additionally, it has shown promise in the treatment of certain genetic disorders associated with abnormal glycosylation. This compound plays a crucial role in drug discovery and development, paving the way for innovative therapeutic interventions. Synonyms: 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-[(1-oxopropyl)amino]-D-mannopyranose. Grades: ≥ 95%. CAS No. 379219-32-6. Molecular formula: C17H25NO10. Mole weight: 403.38. |  |
| D-Mannosamine HCl | D-Mannosamine HCl, a paramount substance pervasively utilized in the biomedical sector, assumes a pivotal role. Its multifaceted properties enable its extensive application towards mitigating an array of ailments and disorders. Within the realm of pharmaceutical advancements, this compound assumes a critical function, facilitating the creation of antiviral pharmaceuticals, antibiotics, and anticancer therapeutics. Invaluable therapeutic implementations encompass combatting viral infections, impeding bacterial proliferation, and efficacious cancer control. The prodigious potential of D-Mannosamine HCl emerges as an instrumental asset in propelling cutting-edge biomedical exploration, thus catalyzing revolutionary drug discoveries. Synonyms: ManNH2 HCl; 2-Amino-2-deoxy-D-mannose HCl; D-Mannosamine Hydrochloride; D-Mannose, 2-amino-2-deoxy-, hydrochloride (1:1). Grades: ≥95%. CAS No. 5505-63-5. Molecular formula: C6H14ClNO5. Mole weight: 215.63. | |
| D-Mannosamine hydrochloride | 1g Pack Size. Group: Biochemicals, Building Blocks. Formula: C6H13NO5 ·HCl. CAS No. 5505-63-5. Prepack ID 15934887-1g. Molecular Weight 215.63. See USA prepack pricing. |  |
| D-Mannosamine hydrochloride | D-Mannosamine hydrochloride is a six-carbon glycoamine that is an amino derivative of D-mannose. D-mannoamine plays a variety of important biological roles in cells [1]. Uses: Scientific research. Group: Natural products. Alternative Names: (2S,3R,4S,5R)-2-Amino-3,4,5,6-tetrahydroxyhexanal hydrochloride. CAS No. 5505-63-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-W021425. |  |
| N-Acetyl-D-[1-13C]mannosamine | N-Acetyl-D-[1-13C]mannosamine. Group: Biochemicals. Alternative Names: 2-Acetamido-2-deoxy-D-[1-13C]mannose. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C713CH15NO6, Molecular Weight: 222.2. US Biological Life Sciences. |  Worldwide |
| N-Acetyl-D-[15N]mannosamine | N-Acetyl-D-[15N]mannosamine. Group: Biochemicals. Alternative Names: 2-[15N]Acetamido-2-deoxy-D-mannose. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C8H1515NO6, Molecular Weight: 222.21. US Biological Life Sciences. | Worldwide |
| N-Acetyl-D-[2-13C]mannosamine | N-Acetyl-D-[2-13C]mannosamine. Group: Biochemicals. Alternative Names: 2-Acetamido-2-deoxy-D-[2-13C]mannose. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C713CH15NO6, Molecular Weight: 222.2. US Biological Life Sciences. | Worldwide |
| N-Acetyl D-mannosamine | 2-deoxy-2-N-acetyl-D-mannopyranose. CAS No. 7772-94-3. Product ID: 3-00070. Molecular formula: C8H15NO6. Mole weight: 221.21. Purity: 98+%. Properties: mp 141-144°C. |  |
| N-Acetyl-D-mannosamine | 10g Pack Size. Group: Biochemicals, Carbohydrates. Formula: C8H15NO6. CAS No. 7772-94-3. Prepack ID 13330633-10g. Molecular Weight 221.21. See USA prepack pricing. | |
| N-Acetyl-D-mannosamine | 1g Pack Size. Group: Biochemicals, Carbohydrates. Formula: C8H15NO6. CAS No. 7772-94-3. Prepack ID 13330633-1g. Molecular Weight 221.21. See USA prepack pricing. | |
| N-Acetyl-D-mannosamine | N-Acetyl-D-mannosamine is an indispensable intermediary compound in glycoconjugate synthesis assuming as a precursor for sialic acid production. It empowers the genesis of imperative glycoproteins and glycolipids. Synonyms: ManNAc; N-Acetylmannosamine; NAM; 2-Acetamido-2-deoxy-D-mannose; 2-Acetamido-2-deoxy-D-mannopyranose; N-Acetyl-beta-D-mannosamine; N-((2R,3S,4R,5S,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide; beta-ManNAc. Grades: ≥98%. CAS No. 7772-94-3. Molecular formula: C8H15NO6. Mole weight: 221.21. | |
| N-Acetyl-D-mannosamine | N-Acetyl-D-mannosamine (ManNAc) is an oral active sialic acid precursor that can prevent hypertension by increasing sialylation of IgG , making it a promising candidate for cardiovascular disease research. Additionally, N-Acetyl-D-mannosamine can activate hypocretin ( HCRT ) gene expression in orexin neurons and improve neurodegeneration caused by aging, offering potential avenues for research in neurological disorders [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. Alternative Names: N-Acetylmannosamine; ManNAc. CAS No. 3615-17-6. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-128850. | |
| N-Acetyl-D-mannosamine-6-phosphate disodium salt | N-Acetyl-D-mannosamine-6-phosphate disodium salt is an indispensable compound within the biomedical field, playing a pivotal role in the synthesis of glycoproteins and glycolipids. It holds immense application in studying a wide array of ailments, encompassing malignant neoplasms and hereditary anomalies. Molecular formula: C8H14NO9P 2Na. Mole weight: 345.15. | |
| N-Acetyl-D-mannosamine 99+% (HPLC) | N-Acetyl-D-mannosamine 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 7772-94-3,4773-29-9. Pack Sizes: 1g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| N-Acetyl-D-mannosamine monohydrate | 1g Pack Size. Group: Biochemicals, Building Blocks, Carbohydrates. Formula: C8H15NO6. CAS No. 14131-64-7. Prepack ID 72078431-1g. Molecular Weight 239.22. See USA prepack pricing. | |
| N-Acetyl L-mannosamine | 2-deoxy-2-N-acetyl-L-mannopyranose. Product ID: 3-00233. Molecular formula: C8H15NO6. Mole weight: 221.21. Source : produced by hormonal cell stimulation. | |
| N-acylmannosamine 1-dehydrogenase | Acts on acetyl-D-mannosamine and glycolyl-D-mannosamine. Highly specific. Group: Enzymes. Synonyms: N-acylmannosamine dehydrogenase; N-acetyl-D-mannosamine dehydrogenase; N-acyl-D-mannosamine dehydrogenase; N-acylmannosamine dehydrogenase. Enzyme Commission Number: EC 1.1.1.233. CAS No. 117698-08-5. N-acylmannosamine 1-dehydrogenase. 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-0140; N-acylmannosamine 1-dehydrogenase; EC 1.1.1.233; 117698-08-5; N-acylmannosamine dehydrogenase; N-acetyl-D-mannosamine dehydrogenase; N-acyl-D-mannosamine dehydrogenase; N-acylmannosamine dehydrogenase. Cat No: EXWM-0140. |  |
| N-Acylmannosamine 1-Dehydrogenase from Pseudomonas sp., Recombinant | In enzymology, a N-acylmannosamine 1-dehydrogenase (EC 1.1.1.233) is an enzyme that catalyzes the chemical reaction:N-acyl-D-mannosamine + NAD+<-> N-acyl-D-mannosaminolactone + NADH + H+. Thus, the two substrates of this enzyme are N-acyl-D-mannosamine and NAD+, whereas its 3 products are N-acyl-D-mannosaminolactone, NADH, and H+. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. Group: Enzymes. Synonyms: N-acylmannosamine 1-dehydrogenase; EC 1.1.1.233; N-acylmannosamine dehydrogenase; N-acetyl-D-mannosamine dehydrogenase; N-acyl-D-mannosamine dehydrogenase; N-acylmannosamine dehydrogenase; 117698-08-5. Enzyme Commission Number: EC 1.1.1.233. CAS No. 117698-08-5. N-acylmannosamine 1-dehydrogenase. Mole weight: mol wt ~120 kDa (gel filtration). Activity: > 45 units/mg protein. Storage: -20°C. Form: lyophilized powder; Powder also contains bovine albumin and sucrose. Source: E. coli. Species: Pseudomonas sp. N-acylmannosamine 1-dehydrogenase; EC 1.1.1.233; N-acylmannosamine dehydrogenase; N-acetyl-D-mannosamine dehydrogenase; N-acyl-D-mannosamine dehydrogenase; N-acylmannosamine dehydrogenase; 117698-08-5. Cat No: NATE-0470. | |
| N-acylmannosamine kinase | Acts on the acetyl and glycolyl derivatives. Group: Enzymes. Synonyms: acylmannosamine kinase (phosphorylating); acetylamidodeoxymannokinase; acetylmannosamine kinase; acylaminodeoxymannokinase; acylmannosamine kinase; N-acyl-D-mannosamine kinase; N-acetylmannosamine kinase; ATP:N-acetylmannosamine 6-phosphotransferase. Enzyme Commission Number: EC 2.7.1.60. CAS No. 9027-53-6. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3091; N-acylmannosamine kinase; EC 2.7.1.60; 9027-53-6; acylmannosamine kinase (phosphorylating); acetylamidodeoxymannokinase; acetylmannosamine kinase; acylaminodeoxymannokinase; acylmannosamine kinase; N-acyl-D-mannosamine kinase; N-acetylmannosamine kinase; ATP:N-acetylmannosamine 6-phosphotransferase. Cat No: EXWM-3091. | |
| N-Propanoyl mannosamine | N-Propanoyl mannosamine is a biomedical compound with inhibitory influence on glycosylation processes allowing for efficacious glycoprotein modification. Synonyms: 2-Deoxy-2-[(1-oxopropyl)amino]-D-mannose. CAS No. 79624-37-6. Molecular formula: C9H17NO6. Mole weight: 235.23. | |
| UDP-N-acetyl-D-mannosamine | UDP-N-acetyl-D-mannosamine is a key compound in the biomedical sector, exhibiting indispensability in synthesizing sialic acids, which carry out pivotal functions across diverse biological phenomena. with application in glycoprotein, glycolipid and essential molecule production, it assumes a critical role in cellular communication, immune response modulation and neurobiological processes. Furthermore, its utilization extends to disease research and investigative endeavors regarding cancer, viral infections and genetic anomalies. Synonyms: UDP-ManNAc; UDP-N-acetyl-alpha-D-mannosamine; UDP-N-Acetylmannosamine; UDP-acetylmannosamine; UDP-N-acetyl-D-mannosamine; 26575-17-7; uridine diphosphate N-acetylmannosamine; uridine 5'-[3-(2-acetamido-2-deoxy-alpha-D-mannopyranosyl) dihydrogen diphosphate]; (2R,3S,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen diphosphate (non-preferred name); CHEBI:68678; LFTYTUAZOPRMMI-ZYQOOJPVSA-N; DTXSID701313724; UD1; [(2R,3S,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] [[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate; C01170; Q27137103; UD9. CAS No. 26575-17-7. Molecular formula: C17H27N3O17P2. Mole weight: 607.35. | |
| UDP-N-acetyl-D-mannosamine dehydrogenase | Part of the pathway for acetamido sugar biosynthesis in bacteria and archaea. The enzyme has no activity with NADP+. Group: Enzymes. Synonyms: UDP-ManNAc 6-dehydrogenase; wecC (gene name). Enzyme Commission Number: EC 1.1.1.336. 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-0250; UDP-N-acetyl-D-mannosamine dehydrogenase; EC 1.1.1.336; UDP-ManNAc 6-dehydrogenase; wecC (gene name). Cat No: EXWM-0250. | |
| 2,3,5-Tri-O-benzyl-D-arabinofuranose | 2,3,5-Tri-O-benzyl-D-arabinofuranose is an aldopentose sugar that functions as an intermediate in the synthesis of phosphono analog of N-acetyl-α-D-mannosamine 1-phosphate from D-arabinose. Group: Biochemicals. Grades: Highly Purified. CAS No. 160549-10-0. Pack Sizes: 500mg, 1g. Molecular Formula: C26H28O5. US Biological Life Sciences. | Worldwide |
| 2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-b-D-mannopyranose | 2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-b-D-mannopyranose, a chemical compound with remarkable properties, is widely employed in the synthesis of glycosylated natural products and pharmaceuticals. This compound, boasting a wide range of potential applications, is adept at the development of glycoconjugates for research into diseases particularly bacterial and viral infections. Incorporating 2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-b-D-mannopyranose into your research endeavors guarantees outstanding results. Synonyms: Tetra-O-acetyl-2-acetamido-2-deoxy-β-D-mannose; 1,3,4,6-Tetra-O-acetyl-2-acetamido-2-deoxy-b-D-mannose; b-D-Mannosamine pentaacetate; (2S,3S,4R,5S,6R)-3-Acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate. Grades: ≥95%. CAS No. 6730-10-5. Molecular formula: C16H23NO10. Mole weight: 389.35. | |
| 2-acetamido-2-deoxy-D-mannose | 2-acetamido-2-deoxy-D-mannose is an essential precursor of N-acetylneuraminic acid (NeuAc), the specific monomer of bacterial capsular polysialic acid (PA). Synonyms: D-Mannose, 2-(acetylamino)-2-deoxy-; Mannose, 2-acetamido-2-deoxy-, D-; 2-(Acetylamino)-2-deoxy-D-mannose; N-Acetyl-D-mannosamine; N-Acetylmannosamine; N-Acetyl-2-amino-2-deoxy-D-mannose; 2-Acetamido-2-deoxy-D-mannose; N-Acetyl-β-D-mannosamine; 2-Acetamido-2-deoxy-D-mannopyranose; D-N-Acetylmannosamine. Grades: >98.0%(LC). CAS No. 3615-17-6. Molecular formula: C8H15NO6. Mole weight: 221.21. | |
| 2-Acetamido-2-deoxy-L-mannopyranose | 2-Acetamido-2-deoxy-L-mannopyranose is a crucial constituent used extensively in the biomedical industry. This compound possesses significant potential for the development of pharmaceutical drugs targeting various diseases. It serves as a key building block in the synthesis of glycosides and carbohydrates, playing a vital role in the treatment of conditions associated with carbohydrate metabolism disorders, such as diabetes mellitus and metabolic syndrome. Its unique chemical structure and therapeutic properties make it an essential component in drug research and development. Synonyms: 2-Acetamido-2-deoxy-L-mannose N-Acetyl-L-mannosamine L-Mannac. CAS No. 6813-82-7. Molecular formula: C8H15NO6. Mole weight: 221.2. | |
| 2-Amino-2-deoxy-D-idose | 2-Amino-2-deoxy-D-idose, a rather uncommon amino sugar that is present in the cell walls of gram-negative bacteria, displays promising potential as an antibacterial agent against methicillin-resistant Staphylococcus aureus (MRSA) by impeding the production of peptidoglycan in bacterial cell walls. Further research has also investigated its potential for cancer treatment as it has exhibited the ability to hinder the growth and proliferation of cancerous cells. This compound's properties offer a comprehensive view of its potential therapeutic applications. Synonyms: 2-amino-3,4,5,6-tetrahydroxyhexanal; 2-Amino-2-deoxyhexose; 6915-39-5; 579-32-8; 7535-00-4; 72904-60-0; 14307-02-9; Galactose, 2-amino-2-deoxy-; Hexose, 2-amino-2-deoxy-; 2-Amino-2-deoxyhexose #; SCHEMBL2560773; CHEMBL4777590; DTXSID90865463; FZHXIRIBWMQPQF-UHFFFAOYSA-N; BCP30031; 3-QUINOXALIN-2-YL-ACRYLICACID; SB45341; SB45694; SY288134; FT-0624549; FT-0773918; EN300-86064; A66741BE-8D02-48CA-9ABE-AC5F6085EB5F; 2-Amino-2-deoxy-D-manno-hexose; Aldehydo-D-mannosamine. CAS No. 579-32-8. Molecular formula: C6H13NO5. Mole weight: 179.17. | |
| Methyl 2-amino-2-deoxy-a-D-mannopyranoside | Methyl 2-amino-2-deoxy-a-D-mannopyranoside is an indispensable compound within the biomedical sector, showcasing immense prospects in studying a plethora of ailments encompassing cancer, diabetes and bacterial infections. This compound has intrinsic capacity to emulate distinct carbohydrates. Synonyms: methyl α-D-mannosamine; (2R,3S,4R,5S,6S)-5-Amino-2-hydroxymethyl-6-methoxy-tetrahydro-pyran-3,4-diol; 1-O-Methyl-alpha-D-mannosamine. CAS No. 50991-93-0. Molecular formula: C7H15NO5. Mole weight: 193.20. | |
| N-acetyl glucosaminyl diphosphoundecaprenol N-acetyl-β-D-mannosaminyltransferase | Involved in the biosynthesis of teichoic acid linkage units in bacterial cell walls. Group: Enzymes. Synonyms: uridine diphosphoacetyl -mannosamineacetyl glucosaminyl pyrophosphoryl undecaprenol acetylmannosaminyltransferase; N-acetylmannosaminyltransferase; UDP-N-acetylmannosamine:N-acetylglucosaminy. Enzyme Commission Number: EC 2.4.1.187. CAS No. 118731-82-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2413; N-acetyl glucosaminyl diphosphoundecaprenol N-acetyl-β-D-mannosaminyltransferase; EC 2.4.1.187; 118731-82-1; uridine diphosphoacetyl -mannosamineacetyl glucosaminyl pyrophosphoryl undecaprenol acetylmannosaminyltransferase; N-acetylmannosaminyltransferase; UDP-N-acetylmannosamine:N-acetylglucosaminyl diphosphorylundecaprenol N-acetylmannosaminyltransferase; UDP-N-acetyl-D-mannosamine:N-acetyl-β-D-glucosaminyldiphosphoundecaprenol β-1,4-N-acetylmannosaminyltransferase; UDP-N-acetyl-D-mannosamine:N-acetyl-β-D-glucosaminyldiphosphoundecaprenol 4-β-N-acetylmannosaminyltransferase; tagA (gene name); tarA (gene name); UDP-N-acetyl-α-D-mannosamine:N-acetyl-β-D-glucosaminyl-diphospho-ditrans,octacis-undecaprenol 4-β-N-acetylmannosaminyltransferase. Cat No: EXWM-2413. | |
| N-acetylhexosamine 1-kinase | This enzyme is involved in the lacto-N-biose I/galacto-N-biosedegradation pathway in the probiotic bacterium Bifidobacterium longum. Differs from EC 2.7.1.157, N-acetylgalactosamine kinase, as it can phosphorylate both N-acetylgalactosamine and N-acetylglucosamine at similar rates. Also has some activity with N-acetyl-D-mannosamine, D-talose and D-mannose as substrate. ATP can be replaced by GTP or ITP but with decreased enzyme activity. Requires a divalent cation, with Mg2+ resulting in by far the greatest stimulation of enzyme activity. Group: Enzymes. Synonyms: NahK; LnpB; N-acetylgalactosamine/N-acetylglucosamine 1-kinase. Enzyme Commission Number: EC 2.7.1.162. N-Acetylhexosamine 1-Kinase. 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-2992; N-acetylhexosamine 1-kinase; EC 2.7.1.162; NahK; LnpB; N-acetylgalactosamine/N-acetylglucosamine 1-kinase. Cat No: EXWM-2992. | |
| N-Acetylneuraminic Acid Aldolase | N-Acetylneuraminic Acid Aldolase. Synonyms: EC 4.1.3.3;N-ACETYLNEURAMINIC ACID ALDOLASE;N-ACETYLNEURAMINIC ACID ALDORASE;N-ACETYLNEURAMINATE PYRUVATE LYASE;NEU5AC ALDOLASE;N-Acetylneuraminic Acid Aldolase from microorganisms;N-ACETYLNEURAMINIC ACID ALDOLASE, FROM MICROORGANISM;N-Acetylneuraminate Pyruvate Lyase, N-Acetylneuraminic Acid Lyase, NANA Aldolase, Sialic Aldolase. CAS No. 9027-60-5. Pack Sizes: 1 kg. Product ID: CDF4-0055. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; N-Acetylneuraminic Acid Aldolase; CDF4-0055; 9027-60-5; 9027-60-5. Purity: 0.99. Color: Slightly yellow. Physical State: Powder. Storage: -20°C. Product Description: Sialic acid aldolases, or N-acetylneuraminate lyases, catalyze the reversible aldol cleavage of N-acetylneuraminic acid to form pyruvate and N-acetyl-D-mannosamine. In nature, N-acetylneuraminate lyase mainly occurs in pathogens. |  |
| Native Escherichia coli N-Acetylneuraminic Acid Aldolase | In enzymology, a N-acetylneuraminate lyase (EC 4.1.3.3) is an enzyme that catalyzes the chemical reaction:N-acetylneuraminate<-> N-acetyl-D-mannosamine + pyruvate. Hence, this enzyme has one substrate, N-acetylneuraminate, and two products, N-acetyl-D-mannosamine and pyruvate. This enzyme belongs to the family of lyases, specifically the oxo-acid-lyases, which cleave carbon-carbon bonds. This enzyme participates in aminosugars metabolism. Applications: This enzyme is useful for enzymatic determination of n-acetylneuraminic acid and sialic acid when coupled with the related enzymes in clinical analysis. for industrial use, this enzyme is useful for enzymatic synthe...o. 9027-60-5. NALase. Mole weight: mol wt ~98 kDa. Activity: > 20 units/mg protein (biuret). Storage: -20°C. Form: Lyophilized powder containing potassium phosphate buffer salt. Source: Escherichia coli. N-acetylneuraminic acid aldolase; acetylneuraminate lyase; sialic aldolase; sialic acid aldolase; sialate lyase; N-acetylneuraminic aldolase; neuraminic aldolase; N-acetylneuraminate aldolase; neuraminic acid aldolase; N-acetylneuraminic acid aldolase; neuraminate aldolase; N-acetylneuraminic lyase; N-acetylneuraminic acid lyase; NPL; NALase; NANA lyase; acetylneuraminate pyruvate-lyase; N-acetylneuraminate pyruvate-lyase; 9027-60-5; EC 4.1.3.3. Cat No: NATE-0490. | |
| Native Microorganism N-Acetylneuraminic acid aldolase | In enzymology, a N-acetylneuraminate lyase (EC 4.1.3.3) is an enzyme that catalyzes the chemical reaction: N-acetylneuraminate <-> N-acetyl-D-mannosamine + pyruvate. Hence, this enzyme has one substrate, N-acetylneuraminate, and two products, N-acetyl-D-mannosamine and pyruvate. This enzyme belongs to the family of lyases, specifically the oxo-acid-lyases, which cleave carbon-carbon bonds. Applications: This enzyme is useful for enzymatic determination of n-acetylneuraminic acid and sialic acid when coupled with the related enzymes in clinical analysis. for industrial use, this enzyme is useful for enzymatic synthesis of sialic acid. Group: Enzymes. Synonyms: N-Ace...ity: Grade III 15U/mg-solid or more (30U/mg-protein or more), (containing approx. 30% of stabilizers). Stability: Stable at-20°C for at least 6 months. Appearance: Yellowish amorphous powder, lyophilized. Form: Freeze dried powder. Source: Microorganism. N-Acetylneuraminate Pyruvate Lyase; N-Acetylneuraminic Acid Lyase; NANA Aldolase; EC 4.1.3.3; N-acetylneuraminate pyruvate-lyase (N-acetyl-D-mannosamine-forming); N-acetylneuraminic acid aldolase; acetylneuraminate lyase; sialic aldolase; sialic acid aldolase; sialate lyase; N-acetylneuraminic aldolase; neuraminic aldolase; N-acetylneuraminate aldolase; neuraminic acid aldolase; N-acetylneuraminic acid aldolase; neu | |
| Sialic Acid Aldolase from Escherichia coli K12, Recombinant | In enzymology, a N-acetylneuraminate lyase (EC 4.1.3.3) is an enzyme that catalyzes the chemical reaction:N-acetylneuraminate<-> N-acetyl-D-mannosamine + pyruvate. Hence, this enzyme has one substrate, N-acetylneuraminate, and two products, N-acetyl-D-mannosamine and pyruvate. This enzyme belongs to the family of lyases, specifically the oxo-acid-lyases, which cleave carbon-carbon bonds. This enzyme participates in aminosugars metabolism. Sialic acid aldolases, or n-acetylneuraminate lyases, catalyze the reversible aldol cleavage of n-acetylneuraminic acid to form pyruvate and n-acetyl-d-mannosamine. in nature, n-acetylneuraminate lyase mainly occurs in pathogen...neuraminate pyruvate-lyase; N-acetylneuraminate pyruvate-lyase. Enzyme Commission Number: EC 4.1.3.3. CAS No. 9027-60-5. NALase. Activity: > 3.0 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing Tris-HCl and NaCl. Source: E. coli BL21. Species: Escherichia coli K12. EC 4.1.3.3; Sialic Acid Aldolase; N-Acetylneuraminate lyase; N-Acetylneuraminate pyruvate-lyase (N-acetyl-D-mannosamine-forming); N-acetylneuraminic acid aldolase; acetylneuraminate lyase; sialic aldolase; sialate lyase; N-acetylneuraminic aldolase; neuraminic aldolase; N-acetylneuraminate aldolase; neuraminic acid aldolase; N-acetylneuraminic acid aldolase; neuraminate aldolase; N | |
| D-Mannosaminuronic acid | | |
| lipopolysaccharide N-acetylmannosaminouronosyltransferase | Involved in the biosynthesis of common antigen in Enterobacteriaceae. Group: Enzymes. Synonyms: ManNAcA transferase; uridine diphosphoacetyl mannosaminuronate-acetyl glucosaminyl pyrophosphoryl undecaprenol acetylmannosaminuronosyltransferase; UDP-N-acetyl-β-D-mannosaminouronate:lipid I N-acetyl-β-D-mannosaminouronosyltransferase (incorrect). Enzyme Commission Number: EC 2.4.1.180. CAS No. 113478-30-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2406; lipopolysaccharide N-acetyl mannosaminouronosyl transferase; EC 2.4.1.180; 113478-30-1; ManNAcA transferase; uridine diphosphoacetyl mannosaminuronate-acetyl glucosaminyl pyrophosphoryl undecaprenol acetylmannosaminuronosyltransferase; UDP-N-acetyl-β-D-mannosaminouronate:lipid I N-acetyl-β-D-mannosaminouronosyltransferase (incorrect). Cat No: EXWM-2406. | |
| N-Acetyl-D-mannosaminuronic acid | Synonyms: Mannacua; N-Acetylmannosaminuronic acid; N-Acetyl-D-mannosaminuronic acid; 57496-35-2; 32TW3B2ZFO; Mannuronic acid, 2-acetamido-2-deoxy-; Mannuronic acid, 2-(acetylamino)-2-deoxy-; D-Mannuronic acid, 2-(acetylamino)-2-deoxy-; 32452-11-2; UNII-32TW3B2ZFO; SCHEMBL1311637; DTXSID40206105; 2-acetamido-2-deoxymannuronic acid; Q27256190. Molecular formula: C8H13NO7. Mole weight: 235.19. | |
| N-Acetyl-D-mannosaminuronic acid sodium | N-Acetyl-D-mannosaminuronic acid sodium, a fundamental component of hyaluronic acid, is widely applied in biomedicine. This versatile compound exhibits remarkable potential in the management of joint pathologies, skin senescence, and tissue regeneration via its moisture-attracting properties. Moreover, it emulates antibacterial interventions, providing a potential antidote to varying microbial pathogens. Synonyms: 5-acetamido-2,3,4-trihydroxy-6-oxohexanoic acid; 2-Acetamido-2-deoxy-D-glucuronicAcid; 34047-66-0; 32452-11-2; NSC256961; SCHEMBL23933730; NSC-256961. Grades: 95%. CAS No. 32452-11-2. Molecular formula: C8H12NO7Na. Mole weight: 257.17. | |
| UDP-N-acetyl-D-mannosaminuronic acid | Synonyms: Udp-N-acetyl-D-mannosaminuronic acid; UDP-N-acetyl-alpha-D-mannosaminouronic acid; UDP-N-acetyl-2-amino-2-deoxy-D-mannuronate; uridine 5'-[3-(2-acetamido-2-deoxy-alpha-D-mannopyranosyluronic acid) dihydrogen diphosphate]; (2s,3s,4r,5s,6r)-5-Acetamido-6-[[[(2r,3s,4r,5r)-5-[2,4-Bis(Oxidanylidene)pyrimidin-1-Yl]-3,4-Bis(Oxidanyl)oxolan-2-Yl]methoxy-Oxidanyl-Phosphoryl]oxy-Oxidanyl-Phosphoryl]oxy-3,4-Bis(Oxidanyl)oxane-2-Carboxylic Acid; UDP-N-acetyl-alpha-D-mannosaminuronate; C06240; CHEBI:70738; (2S,3S,4R,5S,6R)-5-acetamido-6-[[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-3,4-dihydroxyoxane-2-carboxylic acid; J-700273; Q27139053; (2S, 3S, 4R, 5S, 6R)-5- (acetylamino)-6-{[ (R)-{[ (R)-{[ (2R, 3S, 4R, 5R)-5- (2, 4-dioxo-3, 4-dihydropyrimidin-1 (2H)-yl)-3, 4-dihydroxytetrahydrofuran-2-yl]methoxy} (hydroxy)phosphoryl]oxy} (hydroxy)phosphoryl]oxy}-3, 4-dihydroxytetrahydro-2H-pyran-2-carboxylic acid (non-preferred name); SAJ. Molecular formula: C17H25N3O18P2. Mole weight: 621.3. | |
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