| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4-Nitrophenyl α-D-galactopyranoside | 7493-95-0 | sc-220978 sc-220978A | 100 mg 500 mg | $36.00 $95.00 | 1 | |
4-Nitrophenyl α-D-galactopyranoside acts as a substrate for specific glycosidases, showcasing unique interactions with enzyme active sites. Its aromatic nitro group enhances electrophilicity, facilitating nucleophilic attack during hydrolysis. The compound's glycosidic bond exhibits distinct reactivity patterns, influencing reaction kinetics and product formation. Additionally, its solubility characteristics allow for effective diffusion in aqueous environments, impacting enzymatic efficiency and substrate availability. | ||||||
5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-α-D-galactopyranoside | 210110-89-7 | sc-221010 sc-221010A sc-221010B sc-221010C | 5 mg 10 mg 25 mg 50 mg | $350.00 $650.00 $1576.00 $2800.00 | ||
5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-α-D-galactopyranoside serves as a versatile chromogenic substrate, exhibiting selective interactions with glycosidases. The presence of halogen substituents enhances its electrophilic nature, promoting rapid hydrolysis. Its indole moiety contributes to unique photophysical properties, influencing light absorption and emission. The compound's structural conformation allows for specific binding orientations, optimizing enzyme-substrate interactions and reaction rates. | ||||||