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| Product | Description | |
|---|---|---|
| 2-Amino-2-deoxy-D-fucose | 2-Amino-2-deoxy-D-fucose is a highly significant constituent serving as an antecedent in the intricate amalgamation of polysaccharides acknowledged as fucosyl-glycans. These glycans, instrumental in cell identification, immunological retort, and inflammatory processes, assume a paramount status. Synonyms: D-Galactose, 2-amino-2,6-dideoxy-; 2-Amino-2,6-dideoxy-D-galactose; D-Fucose, 2-amino-2-deoxy-; Galactose, 2-amino-2,6-dideoxy-, D-; D-Fucosamine. Grades: ≥95%. CAS No. 6931-59-5. Molecular formula: C6H13NO4. Mole weight: 163.17. |  |
| 2-Deoxy-2-fluoro-D-fucose | 2-Deoxy-2-fluoro-D-fucose is an exquisite biomedical tool, acting as an impeding compound. It diligently directs its attention towards distinctive enzymes orchestrating cellular adhesion and migration. By masterfully dismantling these intricate mechanisms, it exhibiting promising capabilities in thwarting the nefarious progressions of tumor metastasis and angiogenesis. Synonyms: 2-Deoxy-2-fluoro-D-fucose; D-0521. Molecular formula: C6H11FO4. Mole weight: 166.15. | |
| a-D-Fucose-1-phosphate | a-D-Fucose-1-phosphate is a pivotal intermediary in the synthetic pathway of fucose-infused glycoconjugates assuming a fundamental part in intricate cellular signaling mechanisms encompassing cellular adhesion and immunomodulation. | |
| D-Fucose | D-Fucose is an imperative biomedical entity assuming a pivotal role within the realm of glycobiology research. Functioning as a monosaccharide, D-Fucose finds extensive utilization in investigating the intricate dynamics of cellular surface interactions and discerning the intricate signaling cascades implicated in disease advancement and immunological retorts. Synonyms: 6-Deoxy-D-galactose; (+)-Fucose; 6-Deoxygalactose; D-(+)-Fucose; D-6-Deoxygalactose; Rhodeose. Grades: ≥98% by HPLC. CAS No. 3615-37-0. Molecular formula: C6H12O5. Mole weight: 164.16. | |
| D-(+)-Fucose | 1g Pack Size. Group: Sugars. Formula: C6H12O5. CAS No. 3615-37-0. Prepack ID 31642524-1g. Molecular Weight 164.16. See USA prepack pricing. |  |
| D-(+)-Fucose | D-(+)-Fucose. Group: Biochemicals. CAS No. 3615-37-0. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| D-(+)-Fucose | D-(+)-Fucose is a nonmetabolizable analogue of l-arabinose. D-(+)-Fucose prevents growth of Escherichia coli B/r on a mineral salts medium plus l-arabinose by inhibiting induction of the l-arabinose operon [1]. D-fucose is a potent inducer of beta-methylgalactoside permease (MGP) [2]. Uses: Scientific research. Group: Natural products. CAS No. 3615-37-0. Pack Sizes: 50 mg; 100 mg. Product ID: HY-N5102. |  |
| TDP-a-D-fucose ammonium salt | TDP-a-D-fucose ammonium salt, a biochemical with vast utility in the synthesis of fucosylated biomolecules, is a substrate analog with proven efficacy in measuring the activity of fucosyltransferases, central players in the biosynthesis of glycan structures found in glycoproteins and glycolipids. In addition, this product has been demonstrated to be of major significance in foundational research related to cancer, immune response, and host-pathogen interactions. Molecular formula: C16H32N4O16P2. Mole weight: 598.39. | |
| 1,2,3,4-Di-O-isopropylidene-a-D-fucopyranose | 1,2,3,4-Di-O-isopropylidene-a-D-fucopyranose is a precursor in synthesizing complex carbohydrates for potential applications in studying various metabolic disorders. Synonyms: 1,2,3,4-Di-O-isopropylidene-alpha-D-fucopyranose; 1,2:3,4-di-O-Isopropylidene-D-fucopyranose; 6-Deoxy-1,2:3,4-di-O-isopropylidene-alpha-D-galactopyranose; (1S, 2R, 6R, 8R, 9S)-4, 4, 8, 11, 11-pentamethyl-3, 5, 7, 10, 12-pentaoxatricyclo[7.3.0.02, 6]dodecane; 6-Deoxy-1,2:3,4-di-O-isopropylidene-alpha-D-galactopyranoside; 1,2,3,4-Di-O-isopropylidene-a-D-fucopyranose; SCHEMBL13328902; MFCD00190867; CS-0452273; (1S,2R,6R,8R,9S)-4,4,8,11,11-pentamethyl-3,5,7,10,12-pentaoxatricyclo[7.3.0.0,dodecane; (3aR,5R,5aS,8aS,8bR)-2,2,5,7,7-pentamethyltetrahydro-3aH-bis[1,3]dioxolo[4,5-b:4',5'-d]pyran; (3AR,5R,5aS,8aS,8bR)-2,2,5,7,7-pentamethyltetrahydro-5H-bis([1,3]dioxolo)[4,5-b:4',5'-d]pyran; 6-DEOXY-1:2,3:4-DI-O-ISOPROPYLIDENE-ALPHA-D-GALACTOPYRANOSE, 1:2,3:4-DI-O-ISOPROPYLIDENE-ALPHA-D-FUCOSE. CAS No. 4026-27-1. Molecular formula: C12H20O5. Mole weight: 244.28. | |
| 1,2-α-L-fucosidase | Highly specific for non-reducing terminal L-fucose residues linked to D-galactose residues by a 1,2-α-linkage. Not identical with EC 3.2.1.111 1,3-α-L-fucosidase. Group: Enzymes. Synonyms: almond emulsin fucosidase; α-(1?2)-L-fucosidase. Enzyme Commission Number: EC 3.2.1.63. CAS No. 37288-45-2. 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-3927; 1,2-α-L-fucosidase; EC 3.2.1.63; 37288-45-2; almond emulsin fucosidase; α-(1?2)-L-fucosidase. Cat No: EXWM-3927. |  |
| 2,3,4-Tri-O-acetyl-alpha-D-fucopyranosyl bromide | 2,3,4-Tri-O-acetyl-alpha-D-fucopyranosyl bromide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: ACETOBROMO-ALPHA-D-FUCOSE;2,3,4-TRI-O-ACETYL-ALPHA-D-FUCOPYRANOSYL BROMIDE. Product Category: Heterocyclic Organic Compound. CAS No. 24404-52-2. Molecular formula: C12H17BrO7. Mole weight: 353.16. Purity: 0.96. IUPACName: [(2R,3S,4S,5R,6R)-4,5-diacetyloxy-6-bromo-2-methyloxan-3-yl] acetate. Canonical SMILES: CC1C(C(C(C(O1)Br)OC(=O)C)OC(=O)C)OC(=O)C. Product ID: ACM24404522. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 4-galactosyl-N-acetylglucosaminide 3-α-L-fucosyltransferase | Normally acts on a glycoconjugate where R (see reaction) is a glycoprotein or glycolipid. This enzyme fucosylates on O-3 of an N-acetylglucosamine that carries a galactosyl group on O-4, unlike EC 2.4.1.65, 3-galactosyl-N-acetylglucosaminide 4-α-L-fucosyltransferase, which fucosylates on O-4 of an N-acetylglucosamine that carries a galactosyl group on O-3. Group: Enzymes. Synonyms: Lewis-negative α-3-fucosyltransferase; plasma α-3-fucosyltransferase; guanosine diphosphofucose-glucoside α1?3-fucosyltransferase; galactoside 3-fu. Enzyme Commission Number: EC 2.4.1.152. CAS No. 39279-34-0. 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-2378; 4-galactosyl-N-acetylglucosaminide 3-α-L-fucosyltransferase; EC 2.4.1.152; 39279-34-0; Lewis-negative α-3-fucosyltransferase; plasma α-3-fucosyltransferase; guanosine diphosphofucose-glucoside α1?3-fucosyltransferase; galactoside 3-fucosyltransferase; GDP-L-fucose:1,4-β-D-galactosyl-N-acetyl-D-glucosaminyl-R 3-L-fucosyltransferase; GDP-β-L-fucose:1,4-β-D-galactosyl-N-acetyl-D-glucosaminyl-R 3-L-fucosyltransferase; GDP-β-L-fucose:1,4-β-D-galactosyl-N-acetyl-D-glucosaminyl-R 3-α-L-fucosyltransferase. Cat No: EXWM-2378. | |
| aldose 1-dehydrogenase [NAD(P)+] | The enzyme from the archaeon Sulfolobus solfataricus shows broad specificity towards aldoses (D-glucose, D-galactose, D-xylose, L-arabinose, 6-deoxy-D-glucose, D-fucose) and can utilize NAD+ and NADP+ with similar catalytic efficiency. It is involved in aldose catabolism via the branched variant of the Entner-Doudoroff pathway. Group: Enzymes. Enzyme Commission Number: EC 1.1.1.359. 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-0275; aldose 1-dehydrogenase [NAD(P)+]; EC 1.1.1.359. Cat No: EXWM-0275. | |
| α-1,3/4-fucosyltransferase from Helicobacter mustelae, 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: Alpha-(1,3/1,4) fucosyltransferase III; Alpha-(1->4)-L-fucosyltransferase; Alpha-4-L-fucosyltransferase; Beta-acetylglucosaminylsaccharide fucosyltransferase; Blood group Lewis alpha-4-fucosyltransferase; Blood-group substance Le(a)-dependent fucosyltransferase; FucT-II; Galactoside 3(4)-L-fucosyltransferase. Enzyme Commission Number: EC 2.4.1.65. CAS No. 37277-69-3. Purity: min 95% by SDS-PAGE. α-fucosyltransferase. Source: E. coli. Species: Helicobacter mustelae. Alpha-(1,3/1,4) fucosyltransferase III; Alpha-(1->4)-L-fucosyltransferase; Alpha-4-L-fucosyltransferase; Beta-acetylglucosaminylsaccharide fucosyltransferase; Blood group Lewis alpha-4-fucosyltransferase; Blood-group substance Le(a)-dependent fucosyltransferase; FucT-II; Galactoside 3(4)-L-fucosyltransferase. Cat No: NATE-1484. | |
| 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. | |
| D-arabinose isomerase | Requires a divalent metal ion (the enzyme from the bacterium Escherichia coli prefers Mn2+). The enzyme binds the closed form of the sugar and catalyses ring opening to generate a form of open-chain conformation that facilitates the isomerization reaction, which proceeds via an ene-diol mechanism. The enzyme catalyses the aldose-ketose isomerization of several sugars. Most enzymes also catalyse the reaction of EC 5.3.1.25, L-fucose isomerase. The enzyme from the bacterium Falsibacillus pallidus also converts D-altrose to D-psicose. cf. EC 5.3.1.4, L-arabinose isomerase. Group: Enzymes. Synonyms: D-arabinose(L-fucose) isomerase; L-fucose isomerase; D-arabinose ketol-isomerase; arabinose isomerase (misleading). Enzyme Commission Number: EC 5.3.1.3. CAS No. 9023-81-8. 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-5469; D-arabinose isomerase; EC 5.3.1.3; 9023-81-8; D-arabinose(L-fucose) isomerase; L-fucose isomerase; D-arabinose ketol-isomerase; arabinose isomerase (misleading). Cat No: EXWM-5469. | |
| dTDP-4-dehydro-6-deoxyglucose reductase | The enzymes from the Gram-negative bacteria Aggregatibacter actinomycetemcomitans and Escherichia coli O52 are involved in activation of fucose for incorporation into capsular polysaccharide O-antigens. The enzyme from the Gram-positive bacterium Anoxybacillus tepidamans (Geobacillus tepidamans) is involved in activation of fucose for incorporation into the organism's S-layer. The enzyme from Escherichia coli O52 has a higher catalytic efficiency with NADH than with NADPH. Group: Enzymes. Synonyms: dTDP-4-keto-6-deoxyglucose reductase; dTDP-D-fucose:NADP+ oxidoreductase; Fcf1; dTDP-6-deoxy-D-xylo-hex-4-ulopyranose reductase. Enzyme Commission Number: EC 1.1.1.266. 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-0172; dTDP-4-dehydro-6-deoxyglucose reductase; EC 1.1.1.266; dTDP-4-keto-6-deoxyglucose reductase; dTDP-D-fucose:NADP+ oxidoreductase; Fcf1; dTDP-6-deoxy-D-xylo-hex-4-ulopyranose reductase. Cat No: EXWM-0172. | |
| D-threo-aldose 1-dehydrogenase | Acts on L-fucose, D-arabinose and L-xylose; the animal enzyme was also shown to act on L-arabinose, and the enzyme from Pseudomonas caryophylli on L-glucose. Group: Enzymes. Synonyms: L-fucose dehydrogenase; (2S,3R)-aldose dehydrogenase; dehydrogenase, L-fucose; L-fucose (D-arabinose) dehydrogenase. Enzyme Commission Number: EC 1.1.1.122. CAS No. 9082-70-6. 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-0026; D-threo-aldose 1-dehydrogenase; EC 1.1.1.122; 9082-70-6; L-fucose dehydrogenase; (2S,3R)-aldose dehydrogenase; dehydrogenase, L-fucose; L-fucose (D-arabinose) dehydrogenase. Cat No: EXWM-0026. | |
| fucokinase | Requires a divalent cation for activity, with Mg2+ and Fe2+ giving rise to the highest enzyme activity. Forms part of a salvage pathway for reutilization of L-fucose. Can also phosphorylate D-arabinose, but more slowly. Group: Enzymes. Synonyms: fucokinase (phosphorylating); fucose kinase; L-fucose kinase; L-fucokinase; ATP:6-deoxy-L-galactose 1-phosphotransferase; ATP:L-fucose 1-phosphotransferase. Enzyme Commission Number: EC 2.7.1.52. CAS No. 37278-00-5. 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-3083; fucokinase; EC 2.7.1.52; 37278-00-5; fucokinase (phosphorylating); fucose kinase; L-fucose kinase; L-fucokinase; ATP:6-deoxy-L-galactose 1-phosphotransferase; ATP:L-fucose 1-phosphotransferase. Cat No: EXWM-3083. | |
| galactoside 2-α-L-fucosyltransferase | Free lactose can act as acceptor. Normally acts on a glycoconjugate where R (see reaction) is a glycoprotein or glycolipid. The action on glycolipid was previously listed as EC 2.4.1.89. Group: Enzymes. Synonyms: blood group H α-2-fucosyltransferase; guanosine diphosphofucose-galactoside 2-L-fucosyltransferase; α-(1?2)-L-fucosyltransferase; α-2-fucosyltransferase; α-2-L-fucosyltransferase; blood-group substance H-dependent fucosyltransferase; guanosine diphosphofucose-glycoprotein 2-α-fucosyltransferase; guanosine diphosphofucose-lactose fucosyltransferase; GDP fuco. Enzyme Commission Number: EC 2.4.1.69. CAS No. 56093-23-3. 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-2612; galactoside 2-α-L-fucosyltransferase; EC 2.4.1.69; 56093-23-3; blood group H α-2-fucosyltransferase; guanosine diphosphofucose-galactoside 2-L-fucosyltransferase; α-(1?2)-L-fucosyltransferase; α-2-fucosyltransferase; α-2-L-fucosyltransferase; blood-group substance H-dependent fucosyltransferase; guanosine diphosphofucose-glycoprotein 2-α-fucosyltransferase; guanosine diphosphofucose-lactose fucosyltransferase; GDP fucose-lactose fucosyltransferase; guanosine diphospho-L-fucose-lactose fucosyltransferase; guanosine | |
| GDP-b-L-Fucose disodium salt | Guanosine 5-diphospho-b-D-fucose. CAS No. 15839-70-0. Product ID: 3-00194. Molecular formula: C16H25N5O15P2Na2. Mole weight: 633.31. |  |
| GDP-L-fucose synthase | Both human and Escherichia coli enzymes can use NADH in place of NADPH to a slight extent. Group: Enzymes. Synonyms: GDP-4-keto-6-deoxy-D-mannose-3,5-epimerase-4-reductase; GDP-L-fucose:NADP+ 4-oxidoreductase (3,5-epimerizing). Enzyme Commission Number: EC 1.1.1.271. CAS No. 113756-18-6. 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-0178; GDP-L-fucose synthase; EC 1.1.1.271; 113756-18-6; GDP-4-keto-6-deoxy-D-mannose-3,5-epimerase-4-reductase; GDP-L-fucose:NADP+ 4-oxidoreductase (3,5-epimerizing). Cat No: EXWM-0178. | |
| GDP-mannose 4,6-dehydratase | The bacterial enzyme requires bound NAD+. This enzyme forms the first step in the biosynthesis of GDP-α-D-rhamnose and GDP-β-L-fucose. In Aneurinibacillus thermoaerophilus L420-91T, this enzyme acts as a bifunctional enzyme, catalysing the above reaction as well as the reaction catalysed by EC 1.1.1.281, GDP-4-dehydro-6-deoxy-D-mannose reductase. Belongs to the short-chain dehydrogenase/reductase enzyme family, having homologous structures and a conserved catalytic triad of Lys, Tyr and Ser/Thr residues. Group: Enzymes. Synonyms: guanosine 5'-diphosphate-D-mannose oxidoreductase; guanosine diphosphomannose oxidoreductase; guanosine diphosphomannose 4,6-dehydratase; GDP-D-mannose dehydratase; GDP-D-mannose 4,6-dehydratase; Gmd; GDP-mannose 4,6-hydro-lyase; GDP-mannose 4,6-hydro-. Enzyme Commission Number: EC 4.2.1.47. CAS No. 37211-59-9. 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-5036; GDP-mannose 4,6-dehydratase; EC 4.2.1.47; 37211-59-9; guanosine 5'-diphosphate-D-mannose oxidoreductase; guanosine diphosphomannose oxidoreductase; guanosine diphosphomannose 4,6-dehydratase; GDP-D-mannose dehydratase; GDP-D-mannose 4,6-dehydratase; Gmd; GDP-mannose 4,6-hydro-lyase; GDP-mannose 4,6-hydro-lyase (GDP-4-dehydro-6-deoxy-D-mannose-forming). Cat No: EXWM-5036. | |
| 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- | |
| L-fucose isomerase | Requires a divalent metal ion (the enzyme from the bacterium Escherichia coli prefers Mn2+). The enzyme binds the closed form of the sugar and catalyses ring opening to generate a form of open-chain conformation that facilitates the isomerization reaction, which proceeds via an ene-diol mechanism. The enzyme from Escherichia coli can also convert D-arabinose to D-ribulose. The enzyme from the thermophilic bacterium Caldicellulosiruptor saccharolyticus also converts D-altrose to D-psicose and L-galactose to L-tagatose. Group: Enzymes. Enzyme Commission Number: EC 5.3.1.25. CAS No. 60063-83-4. 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-5464; L-fucose isomerase; EC 5.3.1.25; 60063-83-4. Cat No: EXWM-5464. | |
| L-fucose mutarotase | This enzyme shows no 1-epimerase activity with D-glucose, L-rhamnose and D-fucose (cf. EC 5.1.3.3, aldose 1-epimerase). Group: Enzymes. Synonyms: FucU; fucose mutarotase; FucM. Enzyme Commission Number: EC 5.1.3.29. 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-5415; L-fucose mutarotase; EC 5.1.3.29; FucU; fucose mutarotase; FucM. Cat No: EXWM-5415. | |
| 1,2,3,4-Tetra-O-acetyl-5-alkynyl-L-fucose | 1,2,3,4-Tetra-O-acetyl-5-alkynyl-L-fucose is a specialized chemical often involved in studies related to cancer treatments. It's a key component in synthesizing innovative pharmaceuticals aimed at combating tumor growth and expansion. Synonyms: 1,2,3,4-Tetra-O-acetyl-6,7-dideoxy-L-galacto-hept-6-ynopyranose. CAS No. 935658-91-6. Molecular formula: C15H18O9. Mole weight: 342.30. | |
| 1,2,3,4-Tetra-O-acetyl-a-L-fucopyranose | 1,2,3,4-Tetra-O-acetyl-a-L-fucopyranose, a paramount compound in the biomedical field, finds extensive utility in the synthesis of pharmaceutical agents that combat diverse maladies such as cancer, inflammation, and infectious diseases. Remarkably crucial in the realm of drug discovery and development, this product assumes a paramount position by selectively engaging disease mechanisms, thereby facilitating the efficacious treatment across a multitude of conditions. Synonyms: 1,2,3,4-Tetra-O-acetyl-a-L-fucopyranose; 1,2,3,4-tetra-O-acetyl-alpha-L-fucopyranose; (2S,3S,4R,5R,6S)-6-Methyltetrahydro-2H-pyran-2,3,4,5-tetrayl tetraacetate; [(2S,3R,4R,5S,6S)-4,5,6-triacetyloxy-2-methyloxan-3-yl] acetate; (2S,3R,4R,5S,6S)-4,5,6-TRIS(ACETYLOXY)-2-METHYLOXAN-3-YL ACETATE; Discontinued. See T279255; SCHEMBL7153152; QZQMGQQOGJIDKJ-CSHNMWLISA-N; AKOS027327484; AS-73051; 1,2,3,4-Tetra-O-acetyl-?-L-fucopyranose; CS-0187881; 1,2,3,4-Tetra-O-acetyl-alpha-L(-)-fucose; T72773; A923735; 1,2,3,4-Tetra-O-acetyl-alpha-L-fucopyranose, 95%; 1,2,3,4-tetra-O-acetyl-6-deoxy-alpha-L-galactopyranose; (2S,3S,4R,5R,6S)-6-Methyltetrahydro-2H-pyran-2,3,4,5-tetrayltetraacetate; 1,2,3,4-Tetra-O-acetyl-alpha-L(-)-fucose, Tetra-O-acetyl-alpha-L(-)fucopyranose. CAS No. 64913-16-2. Molecular formula: C14H20O9. Mole weight: 332.3. | |
| 1,3,4-Tri-O-acetyl-2-deoxy-2-fluoro-a-L-fucopyranose | 1,3,4-Tri-O-acetyl-2-deoxy-2-fluoro-a-L-fucopyranose - an organic molecule possessing diverse biological activities, has been regarded as a promising candidate for developing new-generation therapeutic agents. The structural resemblance of this compound to fucose renders it an ideal candidate for targeting fucose-associated physiological processes that underlie pathological conditions like inflammation and tumor metastasis. Its potential as a therapeutic agent has been widely explored, primarily owing to its ability to modulate fucosylation-mediated interactions between cell surface glycoconjugates and their cognate ligands, thereby exhibiting encouraging results. Synonyms: 2-Fluoro-a-L-fucose triacetate; 1,3,4-Tri-O-acetyl-2,6-dideoxy-2-fluoro-a-L-galactopyranose. CAS No. 74554-12-4. Molecular formula: C12H17FO7. Mole weight: 292.26. | |
| 1,3,4-Tri-O-acetyl-2-deoxy-2-fluoro-L-fucose | 2,6-Dideoxy-2-fluoro-L-galactopyranose 1,3,4-Triacetate is a reactant in the preparation of β-purine-diphosphate sugars(GDP-fucose-analogs). Synonyms: Peracetylated 2-fluoro 2-deoxy-L-fucose; (3S,4R,5R,6S)-3-fluoro-6-methyl-tetrahydro-2H-pyran-2,4,5-triyl triacetate; 2-deoxy-2-fluorofucose peracetate; 2-fluorofucose triacetate. Grades: ≥ 97%. CAS No. 188783-78-0. Molecular formula: C12H17FO7. Mole weight: 292.26. | |
| 1,6-α-L-fucosidase | The enzyme from Aspergillus niger does not act on 1,2-, 1,3-, or 1,4-L-fucosyl linkages. Group: Enzymes. Synonyms: α-L-fucosidase; 1,6-L-fucosyl-N-acetyl-D-glucosaminylglycopeptide fucohydrolase. Enzyme Commission Number: EC 3.2.1.127. CAS No. 102925-35-9. 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-3810; 1,6-α-L-fucosidase; EC 3.2.1.127; 102925-35-9; α-L-fucosidase; 1,6-L-fucosyl-N-acetyl-D-glucosaminylglycopeptide fucohydrolase. Cat No: EXWM-3810. | |
| 1-Deoxyfuconojirimycin | It is a potent and specific inhibitor of several alpha-L-fucosidases. Synonyms: DFJ; Deoxyfuconojirimycin; (2S,3R,4S,5R)-2-Methyl-3,4,5-piperidinetriol; 1,5-Dideoxy-1,5-imino-L-fucitol; 1,2,6-Trideoxy-2,6-imino-D-galactitol; L-fuco-Deoxynojirimycin. Grades: ≥95% by HPLC. CAS No. 99212-30-3. Molecular formula: C6H13NO3. Mole weight: 147.17. | |
| 1-Deoxymannojirimycin HCl | It is an inhibitor of α-D-mannosidases (jack bean and calf liver) and mammalian α-L-fucosidase, but it has no glucosidase inhibitory properties. Synonyms: DMI HCl; Deoxymannojirimycin hydrochloride; 1,5-Dideoxy-1,5-imino-D-mannitol hydrochloride; (2R,3R,4R,5R)-2-(Hydroxymethyl)-3,4,5-piperidinetriol hydrochloride; Manno-1-deoxynojirimycin hydrochloride; 3,4,5-Piperidinetriol, 2-(hydroxymethyl)-, hydrochloride, (2R,3R,4R,5R)-; (+)-1-Deoxymannojirimycin hydrochloride. Grades: ≥97%. CAS No. 73465-43-7. Molecular formula: C6H13NO4.HCl. Mole weight: 199.63. | |
| 2,3,4-Tri-O-acetyl-a-L-fucopyranosyl bromide | 2,3,4-Tri-O-acetyl-a-L-fucopyranosyl bromide, a glycosylating agent utilized in organic synthesis, has considerable promise in medicinal chemistry. Its application in the fabrication of fucose-infused medications and inquiry on the correlation between fucosylation, cancer, and inflammation, substantiates its potential in this field. Synonyms: Acetobromofucose 2,3,4-Tri-O-acetyl-6-deoxy-L-galactopyranosyl bromide. CAS No. 16741-27-8. Molecular formula: C12H17BrO7. Mole weight: 353.16. | |
| 2,3,4-Tri-O-acetyl-b-L-fucopyranosyl dibenzyl phosphate | 2,3,4-Tri-O-acetyl-b-L-fucopyranosyl dibenzyl phosphate, a derivative of phosphorylated fucoside, is often employed in the production of glycolipids and glycoproteins. This compound displays a remarkable ability to selectively suppress specific fucosylated glycoenzymes that fuel tumor growth and metastasis, marking it as an excellent candidate for potential cancer therapies. Synonyms: [(2S,3R,4R,5S,6R)-4,5-Diacetyloxy-6-bis(phenylmethoxy)phosphoryloxy-2-methyloxan-3-yl] acetate; 6-Deoxy-beta-L-galactopyranose 2,3,4-triacetate 1-[bis(phenylmethyl) phosphate]; (2R,3S,4R,5R,6S)-2-((bis(benzyloxy)phosphoryl)oxy)-6-methyltetrahydro-2H-pyran-3,4,5-triyl triacetate; SCHEMBL9300189; |A-L-Galactopyranose, 6-deoxy-, 2,3,4-triacetate 1-[bis(phenylmethyl) phosphate]; A889013; beta-L-Galactopyranose, 6-deoxy-, 2,3,4-triacetate 1-[bis(phenylmethyl) phosphate]; (2R,3S,4R,5R,6S)-4,5-bis(acetyloxy)-2-{[bis(benzyloxy)phosphoryl]oxy}-6-methyloxan-3-yl acetate. CAS No. 128473-05-2. Molecular formula: C26H31O11P. Mole weight: 550.49. | |
| 2'',3'',4''-Tri-O-benzylfucosyllactose | 2'',3'',4''-Tri-O-benzylfucosyllactose, a complex carbohydrate, serves as an invaluable tool for deciphering the intricate interplay between pathogenic bacteria and their host cells. Researchers have extensively explored its potential as a therapeutic agent, particularly in the context of combatting devastating conditions like tuberculosis and pneumonia. In addition, this compound serves as an indispensable reference standard, enabling scientists to precisely investigate the role that fucosylated glycans play in cellular signaling and interactions. Grades: 90%. Molecular formula: C39H50O15. Mole weight: 758.81. | |
| 2,3-Di-O-benzyl-4-deoxy-L-fucose | 2,3-Di-O-benzyl-4-deoxy-L-fucose is a vital component in the biomedical industry. Its applications include its use in the synthesis of potential antitumor drug derivatives and the treatment of various diseases related to irregular glycogen metabolism. Synonyms: 2,3-Di-O-benzyl-4,6-dideoxy-L-xylo-hexose. CAS No. 191036-43-8. Molecular formula: C20H24O4. Mole weight: 328.4. | |
| 2,6-Dideoxy-2-fluoro-L-galactopyranose 1,3,4-Triacetate | 2,6-Dideoxy-2-fluoro-L-galactopyranose 1,3,4-Triacetate is a reactant in the preparation of β-purine-diphosphate sugars (GDP-fucose-analogs). Group: Biochemicals. Grades: Highly Purified. CAS No. 188783-78-0. Pack Sizes: 25mg, 250mg. Molecular Formula: C12H17FO7, Molecular Weight: 292.26. US Biological Life Sciences. | Worldwide |
| 2,6-Dideoxy-2-fluoro-L-galactopyranose (α, β Mixture) | 2,6-Dideoxy-2-fluoro-L-galactopyranose (α, β Mixture) is used in the preparation of GDP-2-deoxy-2-fluoro- β-L-fucose, a human α-1,3-fucosyltransferase V inhibitor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 100mg. Molecular Formula: C6H11FO4, Molecular Weight: 166.15. US Biological Life Sciences. | Worldwide |
| 2,6-Dideoxy-2-fluoro-L-galactopyranose (α,β Mixture) | 2,6-Dideoxy-2-fluoro-L-galactopyranose (α,β Mixture) is used in the preparation of GDP-2-deoxy-2-fluoro-β-L-fucose, a human α-1,3-fucosyltransferase V inhibitor. Synonyms: 2-Deoxy-2-fluoro-L-fucose. Molecular formula: C6H11FO4. Mole weight: 166.15. | |
| 2-Acetamido-2,6-dideoxy-D-galactose | 2-Acetamido-2,6-dideoxy-D-galactose, an essential constituent in the production of diverse breeds of antimicrobials, embraces macrolides and aminoglycosides. Nevertheless, it also performs a crucial role as an antagonist of N-acetylglucosamine transferase, a pivotal enzyme that facilitates the synthesis of intricate glycoproteins. Moreover, scientific scrutiny has demonstrated that 2-Acetamido-2,6-dideoxy-D-galactose exhibits promising prospects in the treatment of specified bacterial infections and malignant neoplastic diseases. Synonyms: N-Acetyl-D-fucosamine. Molecular formula: C8H15NO5. Mole weight: 205.21. | |
| 2-Acetamido-2,6-dideoxy-L-galactose | 2-Acetamido-2,6-dideoxy-L-galactose, a monosaccharide derivative, has been investigated thoroughly for its diverse applications in the field of bacterial inhibition. Scientific studies reveal a substantial inhibitory potential of this derivative against numerous bacterial strains such as the notorious Staphylococcus aureus, which is responsible for causing infections. Apart from its anti-bacterial properties, it adds further significance as a potential precursor in the production of glycopeptide antibiotics. With remarkable results, this derivative holds tremendous promise in the advancement of new antibiotics. Synonyms: N-Acetyl-L-fucosamine. CAS No. 49694-69-1. Molecular formula: C8H15NO5. Mole weight: 205.21. | |
| 2-Acetamido-2-deoxy-3-O-(a-L-fucopyranosyl)-D-glucopyranose | 2-Acetamido-2-deoxy-3-O-(α-L-fucopyranosyl)-D-glucopyranose is a highly significant compound within the biomedical sector, employed as a facilitator in the research and development of targeted drugs and therapeutic methodologies tailored to cellular receptors and signaling pathways. Synonyms: 3-Fucosyl GlcNAc 2-(Acetylamino)-2-deoxy-3-O-(6-deoxy-a-L-galactopyranosyl)-D-glucopyranose Fuc-a-1,3-GlcNAc. CAS No. 52630-68-9. Molecular formula: C14H25NO10. Mole weight: 367.35. | |
| 2-Amino-2-deoxy-L-arabinose hydrochloride | 2-Amino-2-deoxy-L-arabinose hydrochloride, a pharmacological compound, has gained attention for its antitumor and immunomodulatory properties. Through its potent inhibition of fucosyltransferase (FUT), a key enzyme involved in the formation of Lewis X antigen, it shows promise as a therapeutic agent for an array of malignancies and immunological conditions. The multifaceted mechanisms by which 2-Amino-2-deoxy-L-arabinose hydrochloride exerts its effects requires further study, but the potential for groundbreaking advancements in the field of oncology and immunotherapy cannot be denied. Synonyms: (2R,3R,4S)-2-Amino-3,4,5-trihydroxypentanal hydrochloride; 65982-16-3. CAS No. 65982-16-3. Molecular formula: C5H11NO4.HCl. Mole weight: 185.61. | |
| 2-Amino-2-deoxy-L-fucose | 2-Amino-2-deoxy-L-fucose, a monosaccharide of paramount significance, intricately participates in the inherent complexity of glycan biosynthesis. Its versatile attributes serve as a substrate for fucosyltransferases, inducing the production of fucosylated glycans, a heterogeneous group of biomolecules, meticulously regulating critical biological processes, including cell adhesion and signal transduction. Researchers have also investigated its potential therapeutic applications in ameliorating cancer and inflammatory diseases. Synonyms: 2-Amino-2,6-dideoxy-L-galactose L-Fucosamine. CAS No. 7577-62-0. Molecular formula: C6H13NO4. Mole weight: 163.17. | |
| 2-Chloro-4-nitrophenyl a-L-fucopyranoside | 2-Chloro-4-nitrophenyl α-L-fucopyranoside is a biomedical compound commonly used in research. It acts as a substrate for α-L-fucosidase enzymes, facilitating their study and characterization. This compound enables the investigation of glycan structure and its role in various biological processes. It has potential applications in drug development and understanding diseases associated with aberrant fucosidase activity. Synonyms: CNP-AFU; 2-Chloro-4-nitrophenyl-alpha-L-fucopyranoside; 2-Chloro-4-nitrophenyl a-L-fucopyranoside; (2S,3S,4R,5S,6S)-2-(2-chloro-4-nitrophenoxy)-6-methyloxane-3,4,5-triol; alpha-L-Galactopyranoside, 2-chloro-4-nitrophenyl 6-deoxy-; MFCD04972056; SCHEMBL4263599; DTXSID40463539; EX-A4782; AKOS015899699; AKOS040744200; AC-37021; AS-69565; HY-15911; 2-Chloro-4-nitrophenyl ?-D-Fucopyranoside; 2-Chloro-4-nitrophenyl alpha-D-fucopyranoside; 2-Chloro-4-nitrophenyl alpha -D-Fucopyranoside; 2-Chloro-4-nitrophenyl 6-deoxy-?-L-galactopyranoside; (2S,3S,4R,5S,6S)-2-(2-chloro-4-nitrophenoxy)-6-methyltetrahydro-2H-pyran-3,4,5-triol. CAS No. 157843-41-9. Molecular formula: C12H14ClNO7. Mole weight: 319.69. | |
| 2-Deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)- β-D-glucopyranosyl azide 3,4,6-Triacetate | 2-Deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)- β-D-glucopyranosyl azide 3,4,6-Triacetate is used to synthesize core fucosylated N-glycans and asparagine-linked glycan chains, stereoselectively. Group: Biochemicals. Grades: Highly Purified. CAS No. 102816-24-0. Pack Sizes: 500mg, 5g. Molecular Formula: C20H20N4O9, Molecular Weight: 460.39. US Biological Life Sciences. | Worldwide |
| 2-Deoxy-2-fluoro-L-fucose | 2-Deoxy-2-fluoro-L-fucose, an indispensable compound in the biomedical sector, finds diverse therapeutic applications. Its pivotal role lies in the development of pharmaceutical agents combating ailments like cancer, inflammation, and viral infections. Synonyms: 2,6-dideoxy-2-fluoro-L-Galactose. Grades: ≥95%. CAS No. 70763-62-1. Molecular formula: C6H11FO4. Mole weight: 166.15. | |
| 2-Deoxy-D-galactose | 2-Deoxy-D-galactose is a glucose analog. 2-Deoxy-D-galactose inhibits glycolysis to inhibits tumor growth. 2-Deoxy-D-galactose is a substance interfering with the fucosylation of glycomacromolecules and impairing memory consolidation in various learning tasks. 2-Deoxy-d-galactose hinders glycoprotein fucosylation in vivo [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1949-89-9. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-131892. | |
| 2-Deoxy-L-fucose | 2-Deoxy-L-fucose is a meticulously crafted synthetic sugar molecule, emerging as an indispensable tool for probing the elusive intricacies of protein-carbohydrate interactions and glycosylation processes. Synonyms: 2-Deoxy-L-fucose; 19165-06-1; (3S,4R,5S)-3,4,5-trihydroxyhexanal; 2,6-Dideoxyhexose; 2,6-Dideoxy-L-lyxo-hexose; SCHEMBL3996144; L-lyxo-Hexose, 2,6-dideoxy-; DTXSID30940809. CAS No. 19165-06-1. Molecular formula: C6H12O4. Mole weight: 148.16. | |
| 2'-Fucosyllactose | 2'-Fucosyllactose (2'-FL) is an oligosaccharide that could be derived from human milk. 2'-Fucosyllactose regulates the expression of CD14, alleviates colitis and regulates the gut microbiome. 2'-Fucosyllactose stimulates T cells to increase IFN-γ production and decreases IL-6, IL-17, and TNF-α production of cytokines [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: 2'-FL. CAS No. 41263-94-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N9965. | |
| 2'-Fucosyllactose | 2'-Fucosyllactose (2'-FL) is an oligosaccharide that could be derived from human milk. 2'-Fucosyllactose regulates the expression of CD14, alleviates colitis and regulates the gut microbiome. 2'-Fucosyllactose stimulates T cells to increase IFN-γ production and decreases IL-6, IL-17, and TNF-α production of cytokines. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5-O-DMT-thymidine 3'. Product Category: Inhibitors. Appearance: Off-white solid. CAS No. 41263-94-9. Molecular formula: C18H32O15. Mole weight: 488.44. Purity: 0.9. IUPACName: (2R,3R,4R,5R)-4-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2,3,5,6-tetrahydroxyhexanal. Canonical SMILES: C[C@H]1[C@H]([C@H]([C@@H]([C@@H](O1)O[C@@H]2[C@H]([C@H]([C@H](O[C@H]2O[C@H]([C@@H](CO)O)[C@@H]([C@H](C=O)O)O)CO)O)O)O)O)O. Density: 1.548 g/ml. Product ID: ACM41263949. Alfa Chemistry ISO 9001:2015 Certified. | |
| 2-Fucosyllactose-APD-BSA | 2-Fucosyllactose-APD-BSA is a vital compound in the biomedical industry utilized for drug development. It serving as a valuable tool for studying deciphering glycan recognition processes associated with fucosylated oligosaccharides. This compound aids in investigating therapeutic interventions for reserching diseases like cancer, inflammatory disorders, and viral infections involving fucosylation. Synonyms: Fuc-a-1,2-Gal-b-1,4-Glc-APD-BSA. | |
| 2'-Fucosyllactose-biotin | 2'-Fucosyllactose-biotin, an oligosaccharide with biotin labeling, serves as an effective probe for identifying proteins that bind to fucosylated glycans in research studies. It also facilitates investigating the biological significance of fucosylation in diverse cells and tissues in laboratory settings, however, it doesn't have any therapeutic value in treating medical ailments. Synonyms: 2'FL-biotin. Molecular formula: C36H64N6O16S. Mole weight: 868.99. | |
| 2'Fucosyllactose-BSA(2'FL-BSA) (3 atom spacer) | 2'Fucosyllactose-BSA(2'FL-BSA) (3 atom spacer) is an unrivaled and invaluable instrument utilized in the biomedical discipline to scrutinize and gain comprehension of the association between fucosylated glycans and precise proteins, for instance, pathogen-binding proteins. Its utilization in the research of maladies entailing said connections, for instance, Hepatitis C and HIV, is widely adopted within the scientific community. | |
| 2-Fucosyllactose peracetate | 2-Fucosyllactose peracetate is an invaluable biomedical substance, effectively utilized for studying a myriad of intricate gastrointestinal maladies encompassing the vexatious irritable bowel syndrome and the debilitating ulcerative colitis. Molecular formula: C38H52O25. Mole weight: 908.80. | |
| 2'-Fucosyllactose peracetate | 2'-Fucosyllactose peracetate, an intriguing carbohydrate derivative, has sparked interest in biomedicine research, as its therapeutic potential in treating bacterial infections and inflammation within the gut is explored. Additionally, its application in managing neurodegenerative disorders displays a wealth of prospects. Grades: 90%. Molecular formula: C38H52O25. Mole weight: 908.80. | |
| 2H-1-Benzopyran-2-one,7-[(6-deoxy-b-L-galactopyranosyl)oxy]-4-methyl- | 2H-1-Benzopyran-2-one,7-[(6-deoxy-b-L-galactopyranosyl)oxy]-4-methyl-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-Methylumbelliferyl fucoside, M4508_SIGMA, M5510_SIGMA, M8412_SIGMA, 4-Methylumbelliferyl beta-D-fucoside, 4-Methylumbelliferyl beta-L-fucoside, CID3573836, 4-METHYLUMBELLIFERYLalpha-L-FUCOSIDE, 4-METHYLUMBELLIFERYLbeta-L-FUCOSIDE, 4-Methylumbelliferyl beta-D-fucopyranoside, 4-Methylumbelliferyl beta-L-fucopyranoside, 4-Methylumbelliferyl beta-L -fucopyranoside, 4-Methylumbelliferyl alpha-L -fucopyranoside, 4-Methylumbelliferyl alpha-L-rhamnopyranoside, 54322-38-2, 72601-82-2. Product Category: Heterocyclic Organic Compound. Appearance: White to off-white crystalline powder. CAS No. 72601-82-2. Molecular formula: C16H18O7. Mole weight: 322.31. Purity: 0.96. IUPACName: 4-methyl-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-2-one. Canonical SMILES: CC1C(C(C(C(O1)OC2=CC3=C(C=C2)C(=CC(=O)O3)C)O)O)O. Density: 1.441 g/cm³. ECNumber: 276-730-0. Product ID: ACM72601822. Alfa Chemistry ISO 9001:2015 Certified. | |
| 2-Iodoethyl a-L-fucopyranoside | 2-Iodoethyl α-L-fucopyranoside is a specialized compound utilized in biomedical applications acting as a key intermediate in the research and development of pharmaceutical drugs and research chemicals. This compound finding utility in the development of reserchs for various diseases, including cancer and certain viral infections. By facilitating the modification of fucose-containing biomolecules, it contributes to advances in drug discovery. Molecular formula: C8H15IO5. Mole weight: 318.11. | |
| 2-Naphthyl a-L-fucopyranoside | 2-Naphthyl a-L-fucopyranoside is a critical compound extensively used in biomedical research. It serves as a substrate for enzymes like fucosidase and alpha-L-fucosidase, enabling the analysis of their activity. Additionally, this product plays a vital role in studying diseases associated with abnormal fucosylation, such as cancer and congenital disorders. Synonyms: b-Nap-a-L-Fuc b-Naphthyl-a-L-fucopyranoside. CAS No. 63503-05-9. Molecular formula: C16H18O5. Mole weight: 290.31. | |
| 2-Nitrophenyl b-L-fucopyranoside | 2-Nitrophenyl b-L-fucopyranoside is a highly versatile compound, finding extensive application in the enigmatic realm of the biomedical industry. Positioned as a substrate of paramount significance, it remarkably contributes to the imperative detection and meticulous measurement of α-L-fucosidase activity. Synonyms: ONP-b-L-Fuc. Molecular formula: C12H15NO7. Mole weight: 285.25. | |
| 2-O-α-L-Fucopyranosyl-D-galactose | 2-O-α-L-Fucopyranosyl-D-galactose is a compound used in the research of neurodegenerative disorders, such as Alzheimer's disease, by inhibiting the formation of beta-amyloid plaques. Uses: A new type of β-propeller architecture formed by oligomerization and interacting with fucoside, fucosyllactose, and plant xyloglucan. Synonyms: 2-O-(6-Deoxy-α-L-galactopyranosyl)-D-galactose; Blood Group H Disaccharide; Fuc1-α-2Gal. Grades: 97%. CAS No. 24656-24-4. Molecular formula: C12H22O10. Mole weight: 326.3. | |
| 2-O-Fucosyllactulose | 2-O-Fucosyllactulose is an essential compound functioning as a proficient prebiotic. It can adeptly kindle the proliferation of salutary bacteria within the gut. Synonyms: O-6-Deoxy-a-L-galactopyranosyl-(1?2)-O-b-D-galactopyranosyl-(1?4)-D-fructose. CAS No. 1672706-30-7. Molecular formula: C18H32O15. Mole weight: 488.44. | |
| 3-Fucosyllactose | 3-Fucosyllactose (3-Fucosyl-D-lactose) is one of the major fucosylated oligosaccharides found in human breast milk. 3-Fucosyllactose shows prebiotic, immunomodulator, neonatal brain development, and antimicrobial function [1]. Uses: Scientific research. Group: Natural products. Alternative Names: 3-Fucosyl-D-lactose. CAS No. 41312-47-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N10528. | |
| 3-Fucosyllactose | 3-Fucosyllactose (3-Fucosyl-D-lactose) is one of the major fucosylated oligosaccharides found in human breast milk. 3-Fucosyllactose shows prebiotic, immunomodulator, neonatal brain development, and antimicrobial function. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3-FUCOSYLLACTOSE;(2S,3S,4R,5S,6S)-2-[(2R,3R,4S,5R,6S)-3,5-dihydroxy-2-(hydroxymethyl)-6-[(2R,3S,4R,5R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-oxan-4-yl]oxy-6-methyl-oxane-3,4,5-triol;3-FL,α-L-Fuc-(1-3)-[β-D-Gal-(1-4)]-D-Glc;3-Fucosyllactose (3FL);3-FL;α-L-Fuc-(1→3)-[β-D-Gal-(1→4)]-D-Glc. Product Category: Inhibitors. Appearance: Solid. CAS No. 41312-47-4. Molecular formula: C18H32O15. Mole weight: 488.44. Purity: ≥99.0%. Canonical SMILES: O[C@@H]([C@@H]([C@@H]([C@@H](O1)C)O)O)[C@@H]1O[C@H]([C@@H](O)C=O)[C@@H]([C@H](O)CO)O[C@@H]2O[C@@H]([C@@H]([C@@H]([C@H]2O)O)O)CO. Product ID: ACM41312474. Alfa Chemistry ISO 9001:2015 Certified. Categories: Fuc(a1-3)[Gal(b1-4)]Glc. | |
| 3-Fucosyllactose | 3-fucosyllactose is a trisaccharide that is lactose in which the hydroxy group at position 3 of the glucosyl moiety has undergone formal condensation with the anomeric hydroxy group of fucose (6-deoxy-L-galactose) to give the corresponding glycoside. It is one of the major fucosylated oligosaccharides found in human breast milkIt, and has a role as a human metabolite. It is functionally related to a lactose. Synonyms: 3FL; Galb-4(Fuca-3)Glc; O-6-Deoxy-α-L-galactopyranosyl-(1?3)-O-[β-D-galactopyranosyl-(1?4)]-D-glucose; 3-O-α-L-Fucopyranosyllactose; 3-O-Fucosyllactose; 6-deoxy-alpha-L-galactopyranosyl-(1->3)-[beta-D-galactopyranosyl-(1->4)]-D-glucopyranose. Grades: ≥95%. CAS No. 41312-47-4. Molecular formula: C18H32O15. Mole weight: 488.44. | |
| 3-Fucosyllactose-biotin | 3-Fucosyllactose-biotin is a cutting-edge biomedical compound, emerging as an indispensable tool in the realm of research and diagnostics. By meticulously unraveling intricate fucosylation patterns and delving into the realm of disease biomarkers like cancer, inflammation is and autoimmune disorders, this extraordinary concoction assumes the role of a specific probe. Synonyms: 3FL-biotin. Molecular formula: C34H59N5O17S. Mole weight: 841.92. | |
| 3-galactosyl-N-acetylglucosaminide 4-α-L-fucosyltransferase | This enzyme is the product of the Lewis blood group gene. Normally acts on a glycoconjugate where R (see reaction) is a glycoprotein or glycolipid. Although it is a 4-fucosyltransferase, it has a persistent 3-fucosyltransferase activity towards the glucose residue in free lactose. This enzyme fucosylates on O-4 of an N-acetylglucosamine that carries a galactosyl group on O-3, unlike EC 2.4.1.152, 4-galactosyl-N-acetylglucosaminide 3-α-L-fucosyltransferase, which fucosylates on O-3 of an N-acetylglucosamine that carries a galactosyl group on O-4. Enzymes catalysing the 4-α-fucosylation of the GlcNAc in β-D-Gal-(1?3)-β-GlcNAc sequences (with some activity also as 3-α-fucosyltransferases) are present in plants, where the function in vivo is the modification of N-glycans. In addition, the fucTa gene of Helicobacter strain UA948 encodes a fucosyltransferase with both 3-α- and 4-α-fucosyltransferase activities. Group: Enzymes. Synonyms: (Lea)-dependent (α-3/4)-fucosyltransferase; α(1,3/1,4) fucosyltransferase III; α-(1?4)-L-fucosyltransferase; α-4-L-fucosyltransferase; β-acetylglucosaminylsaccharide fucosyltransferase; FucT-II; Lewis α-(1?3/4)-fucosyltransferase; Lewis blood group α-(1?3/4)-fucosyltransferase; Lewis(Le) blood . Enzyme Commi | |
| 3-O-(2-Acetamido-2-deoxy-b-D-glucopyranosyl)-L-fucopyranose | 3-O-(2-Acetamido-2-deoxy-b-D-glucopyranosyl)-L-fucopyranose is a remarkable carbohydrate compound with extensive biomedical applications, exhibiting exceptional potential in research of diverse bacterial infections associated with fucose-utilizing bacteria. Moreover, it showcases its prowess as a complexing agent within drug delivery systems, endowing superior drug stability and heightened bioavailability. Molecular formula: C14H25NO10. Mole weight: 367.35. | |
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