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| Product | Description | |
|---|---|---|
| D-Allose | 250mg Pack Size. Group: Sugars. Formula: C6H12O6. CAS No. 7283-9-2. Prepack ID 50241498-250mg. Molecular Weight 180.16. See USA prepack pricing. |  |
| D-Allose | D-Allose is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 2595-97-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg. Product ID: HY-128741. |  |
| D-Allose-13C | D-Allose-13C. Group: Biochemicals. Alternative Names: D-Allopyranose-13C. Grades: Highly Purified. CAS No. 70849-28-4. Pack Sizes: 10mg. Molecular Formula: C6H12O6, Molecular Weight: 180.14. US Biological Life Sciences. |  Worldwide |
| D-Allose-2-13C | D-Allose-2-13C. Group: Biochemicals. Alternative Names: D-Allopyranose-2-13C. Grades: Highly Purified. Pack Sizes: 10mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| D-Allose-3-13C | D-Allose-3-13C. Group: Biochemicals. Alternative Names: D-Allopyranose-3-13C. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| D-Allose-6-phosphate disodium | D-Allose-6-phosphate disodium is an indispensable biomolecular compound assuming a paramount role in the research of diverse afflictions, notably those targeting metabolic irregularities and correlated maladies. Synonyms: D-Allose, 6-(dihydrogen phosphate)?, sodium salt (1:2). Grades: 95%. CAS No. 1161976-98-2. Molecular formula: C6H11O9PNa2. Mole weight: 304.10. |  |
| D-Allose-6-phosphate disodium salt hydrate | D-Allose-6-phosphate disodium salt hydrate, a dynamic biomedical substance, is renowned for its efficaciousness in combating specific ailments. Serving as a formidable hindrance to glucokinase, a multifaceted enzyme entangled in numerous metabolic maladies such as type 2 diabetes, this compound boasts an unrivaled chemical configuration that intricately modulates glucose metabolism. Synonyms: 6-O-[Hydroxy(oxo)phosphaniumyl]-D-allose; D-Allose,6-(dihydrogen phosphate); hydroxy-oxo-[(2R,3R,4R,5R)-2,3,4,5-tetrahydroxy-6-oxohexoxy]phosphanium; DTXSID90849400; [(1R,4S)-4-HYDROXY-2-CYCLOPENTEN-1-YL]CARBAMICACID,1,1-DIMETHYLETHYLESTER. CAS No. 82259-50-5. Molecular formula: C6H11O9PNa2. Mole weight: 304.10. | |
| 2-Amino-2-deoxy-D-allose hydrochloride | 2-Amino-2-deoxy-D-allose hydrochloride, a prospective therapeutic candidate in cancer treatment, exhibits remarkable potential to impede the growth of malignant cells by inducing apoptosis and suppressing angiogenesis. Additionally, its therapeutic versatility extends to encompass the treatment of inflammation and infectious diseases. Synonyms: D-Allosamine HCl. CAS No. 2861-47-4. Molecular formula: C6H13NO5.HCl. Mole weight: 215.63. | |
| 3-Acetamido-3-deoxy-D-allose | 3-Acetamido-3-deoxy-D-allose is a compound widely employed in the biomedical sector, demonstrating extraordinary antibacterial attributes, thereby holding considerable promise in studying specific bacterial afflictions. Synonyms: 3-ACETAMIDO-3-DEOXY-D-ALLOSE; 102185-26-2; D-Allose, 3-(acetylamino)-3-deoxy-; N-[(2R,3R,4S,5R)-2,4,5,6-tetrahydroxy-1-oxohexan-3-yl]acetamide; SCHEMBL5516462; DTXSID10721133. CAS No. 102185-26-2. Molecular formula: C8H15NO6. Mole weight: 221.21. | |
| 6-Amino-6-deoxy-D-allopyranose hydrochloride | 6-Amino-6-deoxy-D-allopyranose hydrochloride is a pivotal compound in the biomedical sector assuming a antineoplastic and antimicrobial property. It serves as an invaluable instrument for elucidating the intricate biochemical mechanisms entwined with the realm of drug exploration. Synonyms: 6-Amino-6-deoxy-D-allose hydrochloride; DS6AJS9G6R; 6-Amino-6-deoxy-D-allose HCl; EINECS 278-365-2; UNII-DS6AJS9G6R; 76054-78-9; DTXSID10226956; D-ALLOSE, 6-AMINO-6-DEOXY-, HYDROCHLORIDE (1:1); 24384-96-1. CAS No. 24384-96-1. Molecular formula: C6H13NO5.HCl. Mole weight: 215.63. | |
| allose kinase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. Group: Enzymes. Synonyms: allokinase (phosphorylating); allokinase; D-allokinase; D-allose-6-kinase. Enzyme Commission Number: EC 2.7.1.55. CAS No. 9031-78-1. 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-3086; allose kinase; EC 2.7.1.55; 9031-78-1; allokinase (phosphorylating); allokinase; D-allokinase; D-allose-6-kinase. Cat No: EXWM-3086. |  |
| b-D-Allopyranose | b-D-Allopyranose, an essential monosaccharide, finds extensive utility within the biomedicine sector. Its status as a natural product adds to its credibility. Primarily regarded as a precursor, this compound plays a crucial role in synthesizing diverse drugs and compounds. These substances, in turn, cater to combating diabetes, cancer, and viral infections. Remarkably, the distinctiveness of b-D-Allopyranose's structure is attributed to its extraordinary therapeutic benefits. By enhancing glucose metabolism, restraining tumor growth, and countering viral replication, researchers and pharmaceutical enterprises find immense value in this compound. Synonyms: beta-D-allose; beta-D-allopyranose; 7283-09-2; (2R,3R,4R,5S,6R)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol; B-D-ALLOPYRANOSE; JJ05IRR0HO; MFCD00063268; b-d-allose; 1rpj; beta -D-Allose; beta-D,L-Allose.beta.-D-Allose; ?-D-Allose; D(+)- Allose; D-Allose, 98%; UNII-JJ05IRR0HO.BETA.-D-ALLOPYRANOSE; SCHEMBL624762; CHEBI:40656; WQZGKKKJIJFFOK-QZABAPFNSA-N; DTXSID301015883; beta-D-Allopyranose, beta-D-Allose; AKOS024437744; FS-5229; CS-0142451; F73485; beta-D-allose; D-allose; allose; D-ALLOPYRANOSE; W-200609; Q27104464; 9E6E796A-1C95-45F3-8B7A-D05D3DEBE575; (2R,3R,4R,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol. CAS No. 7283-9-2. Molecular formula: C6H12O6. Mole weight: 180.16. | |
| dTDP-4-dehydro-6-deoxy-α-D-gulose 4-ketoreductase | The enzyme forms an activated deoxy-α-D-allose, which is converted to mycinose after attachment to the aglycones of several macrolide antibiotics, including tylosin, chalcomycin, dihydrochalcomycin, and mycinamicin II. Group: Enzymes. Synonyms: dTDP-4-dehydro-6-deoxygulose reductase; tylD (gene name); gerKI (gene name); chmD (gene name); mydI (gene name). Enzyme Commission Number: EC 1.1.1.364. 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-0281; dTDP-4-dehydro-6-deoxy-α-D-gulose 4-ketoreductase; EC 1.1.1.364; dTDP-4-dehydro-6-deoxygulose reductase; tylD (gene name); gerKI (gene name); chmD (gene name); mydI (gene name). Cat No: EXWM-0281. | |
| dTDP-4-dehydro-6-deoxy-D-glucose 3-epimerase | The enzyme is involved in the biosynthetic pathway of dTDP-6-deoxy-α-D-allose, which is converted to mycinose after attachment to the aglycones of several macrolide antibiotics, including tylosin, chalcomycin, dihydrochalcomycin, and mycinamicin II. Group: Enzymes. Synonyms: dTDP-deoxyglucose 3-epimerase; dTDP-4-keto-6-deoxy-D-glucose 3-epimerase; dTDP-4-keto-6-deoxyglucose 3-epimerase; gerF (gene name); tylJ (gene name); chmJ (gene name); mydH (gene name). Enzyme Commission Number: EC 5.1.3.27. 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-5413; dTDP-4-dehydro-6-deoxy-D-glucose 3-epimerase; EC 5.1.3.27; dTDP-deoxyglucose 3-epimerase; dTDP-4-keto-6-deoxy-D-glucose 3-epimerase; dTDP-4-keto-6-deoxyglucose 3-epimerase; gerF (gene name); tylJ (gene name); chmJ (gene name); mydH (gene name). Cat No: EXWM-5413. | |
| L-rhamnose isomerase | Contains two divalent metal ions located at different metal-binding sites within the active site. The enzyme binds the closed ring form of the substrate and catalyses ring opening to generate a form of open-chain conformation that is coordinated to one of the metal sites. Isomerization proceeds via a hydride-shift mechanism. While the enzyme from the bacterium Escherichia coli is specific for L-rhamnose, the enzyme from the bacterium Pseudomonas stutzeri has broad substrate specificity and catalyses the interconversion of L-mannose and L-fructose, L-lyxose and L-xylulose, D-ribose and D-ribulose, and D-allose and D-psicose. Group: Enzymes. Synonyms: rhamnose isomerase; L-rhamnose ketol-isomerase. Enzyme Commission Number: EC 5.3.1.14. CAS No. 9023-84-1. 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-5455; L-rhamnose isomerase; EC 5.3.1.14; 9023-84-1; rhamnose isomerase; L-rhamnose ketol-isomerase. Cat No: EXWM-5455. | |
| Pyranose Oxidase from Coriolus sp., Recombinant | Pyranose oxidase (P2O) catalyzes the oxidation of aldopyranoses at position C-2 to yield the corresponding 2-ketoaldoses. P2O is a homotetrameric protein that contains covalently bound flavin adenine dinucleotide (FAD). The in vivo substrates of P2O are thought to be D-glucose, D-galactose, and D-xylose. They are oxidized to 2-keto-D-glucose (D-arabino-hexos-2-ulose, 2-dehydro-D-glucose), 2-keto-D-galactose (D-lyxo-hexos-2-ulose, 2-dehydro-D-galactose), and 2-keto-D-xylose (D-threopentos-2-ulose, 2-dehydro-D-xylose), respectively. Pyranose oxidase has significant activity with carbohydrates such as, L-sorbose, D-glucono-1,5-lactone, and D-allose. When pyranose oxidase...ults in the formation of hydrogen peroxide. Applications: Pyranose oxidase (p20) is used for the determination of d-glucose and 1,5-anhydroglucitol in clinical analysis. it is used to study the biotransformations of carbohydrates and is used as an important marker for glycemic control in diabetes patients. Group: Enzymes. Synonyms: pyranose oxidase; EC 1.1.3.10; glucose 2-oxidase; pyranose-2-oxidase; 37250-80-9; P2O. Enzyme Commission Number: EC 1.1.3.10. CAS No. 37250-80-9. P2O. Activity: > 2.7 units/mg solid. Storage: -20°C. Source: E. coli. Species: Coriolus sp. pyranose oxidase; EC 1.1.3.10; glucose 2-oxidase; pyranose-2-oxidase; 37250-80-9; P2O. Cat No: NATE-0500. | |
| Pyranose Oxidase from E. coli, Recombinant | Pyranose oxidase (P2O) catalyzes the oxidation of aldopyranoses at position C-2 to yield the corresponding 2-ketoaldoses. P2O is a homotetrameric protein that contains covalently bound flavin adenine dinucleotide (FAD). The in vivo substrates of P2O are thought to be D-glucose, D-galactose, and D-xylose. They are oxidized to 2-keto-D-glucose (D-arabino-hexos-2-ulose, 2-dehydro-D-glucose), 2-keto-D-galactose (D-lyxo-hexos-2-ulose, 2-dehydro-D-galactose), and 2-keto-D-xylose (D-threopentos-2-ulose, 2-dehydro-D-xylose), respectively. Pyranose oxidase has significant activity with carbohydrates such as, L-sorbose, D-glucono-1,5-lactone, and D-allose. When pyranose oxidase catalyzes the oxidation of aldopyranoses, electrons are transferred to molecular oxygen which results in the formation of hydrogen peroxide. Group: Enzymes. Synonyms: pyranose oxidase; EC 1.1.3.10; glucose 2-oxidase; pyranose-2-oxidase; 37250-80-9; P2O. Enzyme Commission Number: EC 1.1.3.10. CAS No. 37250-80-9. P2O. Mole weight: ca. 290 kDa. Activity: > 3 U/mg lyophilizate. Appearance: Yellow lyophilizate. Storage: at -20°C. Source: E. coli. Species: E. coli. pyranose oxidase; EC 1.1.3.10; glucose 2-oxidase; pyranose-2-oxidase; 37250-80-9; P2O. Cat No: NATE-1252. | |
| Pyranose Oxidase from Microorganism | Pyranose oxidase (P2O) catalyzes the oxidation of aldopyranoses at position C-2 to yield the corresponding 2-ketoaldoses. P2O is a homotetrameric protein that contains covalently bound flavin adenine dinucleotide (FAD). The in vivo substrates of P2O are thought to be D-glucose, D-galactose, and D-xylose. They are oxidized to 2-keto-D-glucose (D-arabino-hexos-2-ulose, 2-dehydro-D-glucose), 2-keto-D-galactose (D-lyxo-hexos-2-ulose, 2-dehydro-D-galactose), and 2-keto-D-xylose (D-threopentos-2-ulose, 2-dehydro-D-xylose), respectively. Pyranose oxidase has significant activity with carbohydrates such as, L-sorbose, D-glucono-1,5-lactone, and D-allose. When pyranose oxidase catalyzes the oxidation of aldopyranoses, electrons are transferred to molecular oxygen which results in the formation of hydrogen peroxide. Group: Enzymes. Synonyms: EC 1.1.3.10; glucose 2-oxidase; pyranose-2-oxidase; 37250-80-9; P2O. Enzyme Commission Number: EC 1.1.3.10. CAS No. 37250-80-9. Mole weight: 70kDa (SDS-PAGE). Activity: >10U/mg protein. Storage: Store at -20°C. Form: Yellow power, lyophilized. Source: Microorganism. pyranose oxidase; EC 1.1.3.10; glucose 2-oxidase; pyranose-2-oxidase; 37250-80-9; P2O; PROD. Cat No: NATE-1718. | |
| Phenyl beta-D-galactopyranoside | Phenyl beta-D-galactopyranoside. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Phenylglucoside, Phenyl-beta-D-glucoside, Maybridge3_004400, Phenyl.beta.-d-alloside, Phenyl-.beta.-D-glucoside, Phenyl- beta-D -glucopyranoside, Phenyl-.beta.-D-glucopyranoside, MolPort-001-814-920, HMS1443H22, PHENYL-alpha-D-GLUCOPYRANOSIDE, CID313297, NSC226967, IDI1_015787, 1464-44-4, 4630-62-0. Product Category: Heterocyclic Organic Compound. CAS No. 4630-62-0. Molecular formula: C12H16O6. Mole weight: 256.25. Purity: 0.96. IUPACName: 2-(hydroxymethyl)-6-phenoxyoxane-3,4,5-triol. Canonical SMILES: C1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O. Density: 1.451 g/cm³. Product ID: ACM4630620. Alfa Chemistry ISO 9001:2015 Certified. Categories: 2818-58-8. |  |
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