2. Saccharides
  3. Glyco Building Blocks
  4. Glycosyl Donors

Glycosyl Donors

Glycosyl Donors (37):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-15921
    IPTG 367-93-1 99.93%
    IPTG is a molecular mimic of allolactose, a lactose metabolite that triggers transcription of the lac operon, and it is therefore used to induce protein expression where the gene is under the control of the lac operator.
    IPTG
  • HY-W008125
    Acetobromo-α-D-glucuronic acid methyl ester, 98% 21085-72-3 99.93%
    Acetobromo-α-D-glucuronic acid methyl ester, 98% is a glucuronosyl donor. Acetobromo-α-D-glucuronic acid methyl ester, 98% is applicable to the synthesis of other compounds.
    Acetobromo-α-D-glucuronic acid methyl ester, 98%
  • HY-43747
    α-Acetobromoglucose, contains 1% CaCO3 as stabilizer 572-09-8 98.0%
    α-Acetobromoglucose, contains 1% CaCO3 as stabilizer (Acetobromo-α-D-glucose, contains 1% CaCO3 as stabilizer) is a glycosyl donor that can be used for the synthesis of other active compounds.
    α-Acetobromoglucose, contains 1% CaCO3 as stabilizer
  • HY-I0402
    N-Acetylneuraminic Acid Methyl Ester 2,4,7,8,9-Pentaacetate 73208-82-9
    N-Acetylneuraminic Acid Methyl Ester 2,4,7,8,9-Pentaacetate is a drug intermediate for synthesis of various active compounds.
    N-Acetylneuraminic Acid Methyl Ester 2,4,7,8,9-Pentaacetate
  • HY-W039865
    1-Thio-beta-D-glucose tetraacetate 19879-84-6 99.88%
    1-Thio-beta-D-glucose tetraacetate exhibits cytotoxicity in cells HeLa and human ocular lens epithelium CECH with IC50s of >250 and >200 μM. 1-Thio-beta-D-glucose tetraacetate reveals moderate anticancer property.
    1-Thio-beta-D-glucose tetraacetate
  • HY-W009020
    β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate 7772-79-4
    β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
    β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate
  • HY-22306
    β-D-Glucose pentaacetate 604-69-3 98.0%
    β-D-Glucose Pentaacetate (Penta-O-acetyl-β-D-glucopyranose) is a glucose derivative, which is mainly used to explore the mechanism of insulin secretion.
    β-D-Glucose pentaacetate
  • HY-137201
    2-Phenylethyl β-D-thiogalactoside 63407-54-5 99.87%
    2-Phenylethyl β-D-thiogalactoside is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    2-Phenylethyl β-D-thiogalactoside
  • HY-W039854
    1,2,3,4-Tetra-O-acetyl-β-D-glucopyranose, 96% 13100-46-4
    1,2,3,4-Tetra-O-acetyl-β-D-glucopyranose, 96% (1,2,3,4-Tetra-O-acetyl-beta-D-glucopyranose, 96%) can be used in glycobiology research to study glycosylation mechanisms, glycosidic bond formation, and stereochemistry.
    1,2,3,4-Tetra-O-acetyl-β-D-glucopyranose, 96%
  • HY-W013165
    1,3,4,6-Tetra-O-acetyl-2-amino-2-desoxy-β-D-glucopyranose hydrochloride 10034-20-5
    1,3,4,6-Tetra-O-acetyl-2-amino-2-desoxy-β-D-glucopyranose (hydrochloride) is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
    1,3,4,6-Tetra-O-acetyl-2-amino-2-desoxy-β-D-glucopyranose hydrochloride
  • HY-W011095
    Chloro 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-glucopyranose 3068-34-6 98.0%
    Chloro 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-glucopyranose is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
    Chloro 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-glucopyranose
  • HY-W106550
    α-D-Galactose pentaacetate 4163-59-1 98.0%
    α-D-Galactose pentaacetate (Pentaacetyl-α-D-galactopyranose) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    α-D-Galactose pentaacetate
  • HY-W049706
    α-D-Glucose pentaacetate 604-68-2
    α-D-Glucose pentaacetate (Penta-O-acetyl-α-D-glucopyranose) is a synthetic sugar compound.
    α-D-Glucose pentaacetate
  • HY-W145527
    Phenyl 1-thio-α-D-mannopyranoside 2,3,4,6-tetraacetate 108032-93-5
    Phenyl 1-thio-α-D-mannopyranoside 2,3,4,6-tetraacetate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    Phenyl 1-thio-α-D-mannopyranoside 2,3,4,6-tetraacetate
  • HY-W393498
    Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-β-D-thiogalactopyranoside 1820572-28-8
    Phenyl 2,4, 6-tri-o-acetyl-3-o-allyl-β-d-Thiogalactopyranoside (Gal[246Ac,3All]-β-SPh) is a class of biochemical reagents used for glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It deals with carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. The field is closely related to basic research, biomedicine and biotechnology.
    Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-β-D-thiogalactopyranoside
  • HY-W393741
    Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside 183875-28-7
    Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-bD-galactopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-Glycan recognition and the role of glycans in biological systems. This field is closely related to basic research, biomedicine and biotechnology.
    Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside
  • HY-W145624
    Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 79528-48-6
    Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
    Methyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
  • HY-166966
    2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl trichloroacetimidate 121238-27-5
    2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl trichloroacetimidate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
    2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl trichloroacetimidate
  • HY-W145572
    Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-glucopyranoside 197005-22-4
    Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-glucopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
    Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-glucopyranoside
  • HY-W145610
    Methyl (phenyl 2,3,4-Tri-O-acetyl-1-thio-β-D-glucopyranosid)uronate 62812-42-4
    Methyl (phenyl 2,3,4-Tri-O-acetyl-1-thio-β-D-glucopyranosid)uronate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
    Methyl (phenyl 2,3,4-Tri-O-acetyl-1-thio-β-D-glucopyranosid)uronate