4-Methylumbelliferyl-α-D-Glucopyranoside
CAS: 17833-43-1
Ref. TM-T85134
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50mg | A consultar |
Información del producto
- 4-MU-α-D-Glucopyranoside
- 4-Methylumbelliferyl-α-D-Glucoside
- 4-Methylumbelliferyl-α-D-Glucose
- 2H-1-Benzopyran-2-one, 7-(α-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4-methyl-
- 4-Methylumbelliferyl A-D-Glucopyranoside
- 4-Methylumbelliferyl α-<span class="text-smallcaps">D</span>-glucopyranoside
- 4-Methylumbelliferyl α-<span class="text-smallcaps">D</span>-glucose
- 4-Methylumbelliferyl α-<span class="text-smallcaps">D</span>-glucoside
- 4-Methylumbelliferyl-A-D-Glucoside
- 4-Methylumbelliferyl-Alpha-D-Glucopyranoside
- Ver más sinónimos
- 4-Methylumbelliferyl-Alpha-D-Glucoside
- 4-Mu-Alpha-D-Glc
- 4-methyl-2-oxo-2H-chromen-7-yl alpha-D-glucopyranoside
- 4-methyl-2-oxo-2H-chromen-7-yl alpha-L-galactopyranoside
- 7-(alpha.-D-glucopyranosyloxy)-4-methyl-2H-1-Benzopyran-2-one
- 7-(α-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-4-methyl-2H-1-benzopyran-2-one
- 7-Hydroxy-4-Methylcumarin-Alpha-D-Glucopyranosid
- Coumarin, 7-(α-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4-methyl-
- 7-(α-D-Glucopyranosyloxy)-4-methyl-2H-1-benzopyran-2-one
- Coumarin, 7-(α-D-glucopyranosyloxy)-4-methyl-
- 2H-1-Benzopyran-2-one, 7-(α-D-glucopyranosyloxy)-4-methyl-
4-Methylumbelliferyl-α-D-glucopyranoside serves as a fluorogenic substrate for α-glucosidase, used in enzymatic assays. This compound undergoes cleavage by α-glucosidase, releasing 4-methylumbelliferyl (4-MU), a compound whose fluorescence intensity varies with pH. Specifically, 4-MU exhibits excitation peaks at 320 nm and 360 nm in acidic (pH 1.97-6.72) and alkaline environments (pH 7.12-10.3), respectively, and its emission peak ranges between 445 nm and 455 nm, with brightness increasing as the pH drops. Utilizing these properties, 4-Methylumbelliferyl-α-D-glucopyranoside has been effectively applied in the measurement of α-glucosidase activity within infant blood spot samples, acting as a diagnostic marker for Fabry and Pompe diseases. These illnesses are types of lysosomal storage disorders caused by α-glucosidase enzyme deficiency.
Propiedades químicas
Consulta técnica sobre: TM-T85134 4-Methylumbelliferyl-α-D-Glucopyranoside
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