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| Product | Description | |
|---|---|---|
| D-Glucosamine sulfate | Glucosamine sulfate is present in mucopolysaccharides and in polysaccharides found in bacteria, fungi, higher plants. Glucosamine sulfate has environmental antibacterial activity. Uses: Antiarthritic/antibacterial. Synonyms: Chitosamine Sulphate; 2-Amino-2-deoxy-D-glucose sulphate. Grades: >98%. CAS No. 29031-19-4. Molecular formula: C6H13NO5 H2SO4. Mole weight: 277.25. |  |
| D-Glucosamine sulfate 2NaCl | Cas No. 38899-05-07. | |
| D-Glucosamine sulfate Potassium salt USP | D-Glucosamine sulfate Potassium salt USP. Grades: USP. CAS No. 14999-43-0. Product ID: 3-02732. Molecular formula: C12H28K2N2O14S. Mole weight: 534.62. Properties: sweet powder. |  |
| D-Glucosamine sulfate sodium salt | 2-deoxy-2-sulfamino-D-glucopyranose. CAS No. 38899-05-7. Product ID: 3-00022. Molecular formula: C6H12NO8SNa. Mole weight: 281.16. Purity: 0.96. | |
| D-Glucosamine sulfate sodium salt USP | 2-deoxy-2-sulfamino-D-glucopyranose. Grades: USP. CAS No. 29031-19-4. Product ID: 3-00305. Molecular formula: C12H28N2O14S.2K. Mole weight: 502.4. | |
| D-Glucosamine-2-N,3-O,6-O-trisulfate sodium salt | It is the predominant 3-O-sulfated unit found in the antithrombin binding site in porcine mucosal heparin. Synonyms: 2-Deoxy-2-(sulfoamino)-D-glucose 3,6-bis(hydrogen sulfate) trisodium salt; D-Glucosamine N2,3,6-trisulfate sodium salt. CAS No. 157297-02-4. Molecular formula: C6H10NNa3O14S3. Mole weight: 485.31. | |
| D-Glucosamine 6-sulfate | D-Glucosamine 6-sulfate has been shown as an activator of ribozyme GlmS. Applications: A ribozyme glms activator. Group: Coenzymes. Synonyms: GlcN-6S; D-Glucosamine-6-O-sulphate. CAS No. 91674-26-9. Purity: ≥99%. Mole weight: 259.23. Appearance: Powder. Form: Solid. GlcN-6S; D-Glucosamine-6-O-sulphate; D-Glucosamine 6-sulfate; 91674-26-9. Cat No: COEC-112. |  |
| D-Glucosamine-2-N,3-O-disulphate disodium salt | It is the residue found in the antithrombin binding site in heparin. Synonyms: D-Glucosamine N2,3-disulfate disodium salt; 2-Deoxy-2-sulfamino-D-glucopyranose-3-sulfate disodium salt; [(3R,4R,5R,6R)-2,5-dihydroxy-6-(hydroxymethyl)-3-(sulfonatoamino)oxan-4-yl] sulfate disodium. Grades: ≥95%. CAS No. 112898-34-7. Molecular formula: C6H11NO11S2Na2. Mole weight: 383.25. | |
| D-Glucosamine-3,4,6-tri-O-sulphate trisodium salt | It is a mixed anomer. Synonyms: D-glucosamine 3,4,6-trisulfate sodium; 2-Amino-2-deoxy-D-glucose 3,4,6-tris(hydrogen sulfate) sodium salt; Sodium (2R,3R,4R,5R)-5-amino-2-hydroxy-6-oxohexane-1,3,4-triyl tris(sulfate); Trisodium 2-amino-2-deoxy-3,4,6-tri-O-sulfonato-D-glucopyranose. Grades: ≥95%. CAS No. 157297-03-5. Molecular formula: C6H10NO14S3Na3. Mole weight: 485.31. | |
| D-Glucosamine-3-O-sulphate | It's part of the heparin antithrombin binding site. Synonyms: 3-O-Sulfate glucosamine; glucosamine 3-O-sulfate; D-Glucose, 2-amino-2-deoxy-, 3-(hydrogen sulfate); D-Glucosamine 3-sulfate; 2-Amino-2-deoxy-D-glucose 3-sulfate. Grades: ≥95%. CAS No. 76330-20-6. Molecular formula: C6H13NO8S. Mole weight: 259.23. | |
| D-Glucosamine-6-O-sulphate | It is a component of heparin, heparin sulfate, keratin sulfate, and cell surface glycoconjugates. Synonyms: D-Glucosamine 6-Sulfate; GLCN-6S; {[(2R,3S,4R,5R)-5-amino-2,3,4-trihydroxy-6-oxohexyl]oxy}sulfonic acid; 2-Amino-2-deoxy-6-O-sulfo-D-glucose; D-Glucose, 2-amino-2-deoxy-, 6-(hydrogen sulfate). Grades: ≥95%. CAS No. 91674-26-9. Molecular formula: C6H13NO8S. Mole weight: 259.23. | |
| Glucosamine 6-sulfate | Glucosamine 6-sulfate (GlcN6P) is an organic cofactor that splits phosphodiester bonds. Glucosamine 6-sulfate plays a variety of catalytic roles in glmS ribozymes [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: GlcN6P; D-Glucosamine-6-sulfate. CAS No. 91674-26-9. Pack Sizes: 5 mg; 10 mg. Product ID: HY-W009439. |  |
| Glucosamine sulfate | Glucosamine sulfate (D-Glucosamine sulfate) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, is used as a dietary supplement. Glucosamine sulfate also is a natural constituent of glycosaminoglycans in the cartilage matrix and synovial fluid, which when administered exogenously, exerts pharmacological effects on osteoarthritic cartilage and chondrocytes [1]. Uses: Scientific research. Group: Natural products. Alternative Names: D-Glucosamine sulfate. CAS No. 29031-19-4. Pack Sizes: 500 mg. Product ID: HY-N0487. | |
| Glucosamine Sulfate Sodium Chloride | It appears as a component of heparin and heparin sulfate. Synonyms: D-Glucosamine-2-N-sulfate sodium salt; D-Glucosamine 2-sulfate sodium salt; 2-Deoxy-2-sulfamino-D-glucopyranose sodium salt; GlcN-2S sodium salt; 2-Deoxy-2-sulfoamino-D-glucose Sodium Salt; N-Sulfoglucosamine Sodium Salt. Grades: ≥95%. CAS No. 38899-05-7. Molecular formula: C6H12NNaO8S. Mole weight: 281.22. | |
| Heparin derived disaccharide sodium salt | Heparin derived disaccharide sodium salt is a biomedical product used in the research of blood clotting disorders. This sodium salt compound is derived from heparin, a drug commonly used to prevent and study deep vein thrombosand pulmonary embolism. Synonyms: 2-Deoxy-2-sulfoamino-6-O-sulfo-4-O-(2-O-sulfo-a-L-idopyranuronosyl)-a-D-glucopyranose; 4-O-(a-L-Idopyranosyluronic acid 2-sulfate)-D-glucosamine 2,6-disulfate. CAS No. 98797-50-3. Molecular formula: C12H15NO19S3 Na4. Mole weight: 665.4. | |
| 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. | |
| D-Glucosamine-2-N,6-O-disulphate disodium salt | It is the predominant aminosugar component in heparin. Synonyms: 2-Deoxy-2-(sulfoamino)-D-glucose 6-(hydrogen sulfate) disodium salt; Disodium [ ({ (2R, 3S, 4R, 5R) -2, 3, 4-trihydroxy-6-oxo-5-[ (sulfonatooxy) amino]hexyl}peroxy) sulfonyl]oxidanide. CAS No. 202266-99-7. Molecular formula: C6H11NO11S2Na2. Mole weight: 383.26. | |
| D-Glucosamine-3,6-di-O-sulphate sodium salt | It's part of the heparin antithrombin binding site. Synonyms: Sodium (2R,3R,4R,5R)-5-amino-2,3-dihydroxy-6-oxohexane-1,4-diyl bis(sulfate); 2-Amino-2-deoxy-D-glucose 3,6-bis(hydrogen sulfate) disodium salt. CAS No. 536741-53-4. Molecular formula: C6H11NNa2O11S2. Mole weight: 383.25. | |
| [heparan sulfate]-glucosamine 3-sulfotransferase 1 | This enzyme differs from the other [heparan sulfate]-glucosamine 3-sulfotransferases [EC 2.8.2.29 ([heparan sulfate]-glucosamine 3-sulfotransferase 2) and EC 2.8.2.30 ([heparan sulfate]-glucosamine 3-sulfotransferase 3)] by being the most selective for a precursor of the antithrombin-binding site. It has a minimal acceptor sequence of: ? GlcNAc6S? GlcA? GlcN2S*+/-6S? IdoA2S? GlcN2S?, the asterisk marking the target (symbols as in 2-Carb-38) using +/- to mean the presence or absence of a substituent, and > to separate a predominant structure from a minor one. Thus Glc(N2S > NAc) means a residue of glucosamine where the N carries a sulfo group mainly but occasionally a...sulfotransferase; glucosaminyl 3-O-sulfotransferase; heparan sulfate D-glucosaminyl 3-O-sulfotransferase; isoform/isozyme 1 (3-OST-1, HS3ST1). Enzyme Commission Number: EC 2.8.2.23. CAS No. 183257-54-7. 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-3382; [heparan sulfate]-glucosamine 3-sulfotransferase 1; EC 2.8.2.23; 183257-54-7; heparin-glucosamine 3-O-sulfotransferase; 3'-phosphoadenylyl-sulfate:heparin-glucosamine 3-O-sulfotransferase; glucosaminyl 3-O-sulfotransferase; heparan sulfate D-glucosaminyl 3-O-sulfotransferase; isoform/isozyme 1 (3-OST-1, HS3ST1). Cat No: EXWM-3382. | |
| [heparan sulfate]-glucosamine 3-sulfotransferase 2 | This enzyme sulfates the residues marked with an asterisk in sequences containing at least ? IdoA2S? GlcN*? or ? GlcA2S? GlcN*? (symbols as in 2-Carb-38). Preference for GlcN2S vs. unmodified GlcN has not yet been established. Additional structural features are presumably required for substrate recognition, since the 3-O-sulfated residue is of low abundance, whereas the above IdoA-containing sequence is quite abundant. This enzyme differs from the other [heparan sulfate]-glucosamine 3-sulfotransferases by modifying selected glucosamine residues preceded by GlcA2S; EC 2.8.2.23 ([heparan sulfate]-glucosamine 3-sulfotransferase 1) prefers GlcA or IdoA, whereas EC 2.8.2.30 ([heparan sulfate]-glucosamine 3-sulfotransferase 3) prefers IdoA2S. Group: Enzymes. Synonyms: glucosaminyl 3-O-sulfotransferase; heparan sulfate D-glucosaminyl 3-O-sulfotransferase; isoform/isozyme 2 (3-OST-2, HS3ST2). Enzyme Commission Number: EC 2.8.2.29. 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-3388; [heparan sulfate]-glucosamine 3-sulfotransferase 2; EC 2.8.2.29; glucosaminyl 3-O-sulfotransferase; heparan sulfate D-glucosaminyl 3-O-sulfotransferase; isoform/isozyme 2 (3-OST-2, HS3ST2). Cat No: EXWM-3388. | |
| heparosan-N-sulfate-glucuronate 5-epimerase | The enzyme acts on D-glucosyluronate residues in N-sulfated heparosan polymers, converting them to L-iduronate, thus modifying the polymer to heparan-N-sulfate. The enzyme requires that at least the N-acetylglucosamine residue linked to C-4 of the substrate has been deacetylated and N-sulfated, and activity is highest with fully N-sulfated substrate. It does not act on glucuronate residues that are O-sulfated or are adjacent to N-acetylglucosamine residues that are O-sulfated at the 6 position. Thus the epimerization from D-glucuronate to L-iduronate occurs after N-sulfation of glucosamine residues but before O-sulfation. Not identical with EC 5.1.3.19 chondroitin-glucuronate 5-epimerase or with EC 5.1.3.36, heparosan-glucuronate 5-epimerase. Group: Enzymes. Synonyms: heparosan epimerase; heparosan-N-sulfate-D-gl. Enzyme Commission Number: EC 5.1.3.17. CAS No. 112567-86-9. 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-5402; heparosan-N-sulfate-glucuronate 5-epimerase; EC 5.1.3.17; 112567-86-9; heparosan epimerase; heparosan-N-sulfate-D-glucuronosyl 5-epimerase; C-5 uronosyl epimerase; polyglucuronate epimerase; D-glucuronyl C-5 epimerase; poly[(1,4)-β-D-glucuronosyl-(1,4)-N-sulfo-α-D-glucosaminyl] glucurono-5-epimerase. Cat No: EXWM-5402. | |
| keratan-sulfate endo-1,4-β-galactosidase | Hydrolyses the 1,4-β-D-galactosyl linkages adjacent to 1,3-N-acetyl-α-D-glucosaminyl residues. Also acts on some non-sulfated oligosaccharides, but only acts on blood group substances when the 1,2-linked fucosyl residues have been removed (cf. EC 3.2.1.102 blood-group-substance endo-1,4-β-galactosidase). Group: Enzymes. Synonyms: endo-β-galactosidase (ambiguous); keratan sulfate endogalactosidase; keratanase; keratan-sulfate 1,4-β-D-galactanohydrolase. Enzyme Commission Number: EC 3.2.1.103. CAS No. 55072-01-0. Endo-β-galactosidase. 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-3786; keratan-sulfate endo-1,4-β-galactosidase; EC 3.2.1.103; 55072-01-0; endo-β-galactosidase (ambiguous); keratan sulfate endogalactosidase; keratanase; keratan-sulfate 1,4-β-D-galactanohydrolase. Cat No: EXWM-3786. | |
| 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 | |
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