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Results for "

Methyl 4,6-O-Benzylidene-β-D-glucopyranoside

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Biochemical Assay Reagents (4)

Inhibitors & Agonists

Biochemical Assay Reagents

Cat. No.	상품명	Target	연구분야	Chemical Structure

HY-W011547

**Methyl 4,6-O-Benzylidene-α-D-glucopyranoside**	Biochemical Assay Reagents	Others
Methyl 4,6-O-Benzylidene-α-D-glucopyranoside serves as the starting material for the active intermediate Dibutylstannylene acetals. Using Dibutylstannylene acetals as the starting material, the regioselective synthesis of carbohydrate-based vinyl monomer compounds is successfully achieved .

HY-W153540

**Methyl 4,6-O-Benzylidene-β-D-glucopyranoside**	Biochemical Assay Reagents	Others
Methyl 4,6-O-Benzylidene-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 .

HY-W145615

**Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside**	Biochemical Assay Reagents	Others
Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-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 .

HY-W416359

**Methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-N-phthalimido- β-D-glucopyranoside**	Biochemical Assay Reagents
Methyl 3-O-benzyl-4, 6-O-Benzylidene-2-deoxy-2-N-Phthalimido-β-d-Glucopyranoside is a class of biochemical reagents used in the study of glycobiology. 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 .

Cat. No.	상품명	Type

HY-W011547

**Methyl 4,6-O-Benzylidene-α-D-glucopyranoside**	Biochemical Assay Reagents
Methyl 4,6-O-Benzylidene-α-D-glucopyranoside serves as the starting material for the active intermediate Dibutylstannylene acetals. Using Dibutylstannylene acetals as the starting material, the regioselective synthesis of carbohydrate-based vinyl monomer compounds is successfully achieved .

HY-W153540

**Methyl 4,6-O-Benzylidene-β-D-glucopyranoside**	Biochemical Assay Reagents
Methyl 4,6-O-Benzylidene-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 4,6-O-Benzylidene-β-D-glucopyranoside

Biochemical Assay Reagents

Methyl 4,6-O-Benzylidene-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 .

HY-W145615

**Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside**	Biochemical Assay Reagents
Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-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 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-D-glucopyranoside

Biochemical Assay Reagents

Methyl 2,3-Di-O-benzoyl-4,6-O-benzylidene-α-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 .

HY-W416359

**Methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-N-phthalimido- β-D-glucopyranoside**	Biochemical Assay Reagents
Methyl 3-O-benzyl-4, 6-O-Benzylidene-2-deoxy-2-N-Phthalimido-β-d-Glucopyranoside is a class of biochemical reagents used in the study of glycobiology. 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 .

Methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-N-phthalimido- β-D-glucopyranoside

Biochemical Assay Reagents

Methyl 3-O-benzyl-4, 6-O-Benzylidene-2-deoxy-2-N-Phthalimido-β-d-Glucopyranoside is a class of biochemical reagents used in the study of glycobiology. 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 .

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BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature. Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.

BODIPY 493/503 purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 1;16(1):1241. [Abstract]

MedchemExpress Validation 01

MedchemExpress Validation 03

Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred

MedchemExpress Validation 04

MedchemExpress Validation

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