SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4-Nitrophenyl α-D-galactopyranoside | 7493-95-0 | sc-220978 sc-220978A | 100 mg 500 mg | $37.00 $97.00 | 1 | |
4-Nitrophenyl α-D-galactopyranoside acts as an alpha-gal A by engaging in specific glycosidic bond cleavage, driven by its nitrophenyl group, which enhances electrophilicity. This compound exhibits notable reactivity due to its ability to stabilize transition states during enzymatic hydrolysis. Its structural features promote selective interactions with glycosidases, influencing reaction rates and pathways, while its solubility in various solvents allows for versatile experimental applications. | ||||||
4-Methylumbelliferyl-α- D-galactopyranoside | 38597-12-5 | sc-280454 sc-280454A sc-280454B sc-280454C sc-280454D | 50 mg 100 mg 250 mg 500 mg 1 g | $130.00 $193.00 $312.00 $525.00 $838.00 | 8 | |
4-Methylumbelliferyl-α-D-galactopyranoside serves as a substrate for alpha-galactosidase, showcasing unique fluorescence properties upon enzymatic cleavage. The presence of the methylumbelliferyl moiety enhances its sensitivity to enzymatic activity, allowing for real-time monitoring of hydrolysis. This compound's structural configuration facilitates specific binding interactions with glycosidases, influencing catalytic efficiency and reaction dynamics, while its solubility profile supports diverse analytical techniques. | ||||||
6-Bromo-2-naphthyl-α-D-galactopyranoside | 25997-59-5 | sc-221088 | 100 mg | $360.00 | ||
6-Bromo-2-naphthyl-α-D-galactopyranoside acts as a selective substrate for alpha-galactosidase, characterized by its unique naphthyl group that enhances hydrophobic interactions with the enzyme's active site. This compound exhibits distinct reaction kinetics, with a notable increase in turnover rate due to its sterically favorable structure. Its solubility in organic solvents allows for versatile applications in biochemical assays, while the bromine substituent may influence electronic properties, affecting reactivity and stability. | ||||||