CAS 878495-64-8

Fórmula: C14H15BrClNO6

InChI: InChI=1S/C14H15BrClNO6/c15-6-1-5-8(2-7(6)16)17-3-9(5)22-14-13(21)12(20)11(19)10(4-18)23-14/h1-3,10-14,17-21H,4H2/t10-,11-,12+,13-,14+/m1/s1

Chave InChI: CHRVKCMQIZYLNM-RGDJUOJXSA-N

SMILES: C1=C2C(=CC(=C1Br)Cl)NC=C2O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O

(2R,3R,4S,5S,6R)-2-((5-bromo-6-chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

CAS: 878495-64-8

(2R,3R,4S,5S,6R)-2-((5-bromo-6-chloro-1H-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

Pureza: 95+%

Peso molecular: 408.6300049

Ref: 10-F749756

5-Bromo-6-chloro-3-indolyl α-D-glucopyranoside

CAS: 878495-64-8

5-Bromo-6-chloro-3-indolyl α-D-glucopyranoside

Fórmula: C₁₄H₁₅BrClNO₆

Pureza: By hplc: 99.1% (Typical Value in Batch COA)

Cor e Forma: Solid-Powder

Peso molecular: 408.62899

Ref: 54-BIMB3104

5-Bromo-6-chloro-3-indolyl a-D-glucopyranoside

CAS: 878495-64-8

5-Bromo-6-chloro-3-indolyl a-D-glucopyranoside is a biochemical reagent used in glycobiology research. Glycobiology focuses on the study of the structure, synthesis, biology, and evolution of sugars, encompassing carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan interactions, and the roles of glycans in biological systems. This field is closely linked to fundamental research, biomedicine, and biotechnology.

Fórmula: C₁₄H₁₅BrClNO₆

Cor e Forma: Solid

Peso molecular: 408.63

Ref: TM-TSW-00301

5-Bromo-6-chloro-3-indolyl α-D-glucopyranoside

CAS: 878495-64-8

5-Bromo-6-chloro-3-indolyl α-D-glucopyranoside is a chromogenic substrate that yields a magenta-colored product after cleavage. The chromophore 5-bromo-6-chloro-indoxyl is released, generating the observable color. It is used in Pompe disease diagnostics, a glycogen storage disorder, that measures the deffiency of alpha-glucosidase (GAA) that could lead to the accumulation of glycogen in lysosomes.

Fórmula: C₁₄H₁₅BrClNO₆

Pureza: Min. 95%

Cor e Forma: Powder

Peso molecular: 408.63 g/mol

Ref: 3D-EB03231