| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Deoxyfuconojirimycin hydrochloride | 210174-73-5 | sc-205644 sc-205644A sc-205644B sc-205644C sc-205644D | 1 mg 5 mg 25 mg 50 mg 100 mg | $112.00 $265.00 $479.00 $694.00 $1019.00 | 3 | |
Deoxyfuconojirimycin hydrochloride functions as a potent inhibitor of fucosidases, showcasing remarkable specificity in its interactions with glycosidic bonds. Its structural conformation facilitates strong hydrogen bonding and hydrophobic interactions, enhancing its affinity for target enzymes. The compound's unique stereochemistry influences its binding dynamics, leading to altered reaction pathways and kinetic profiles, which can significantly impact enzymatic activity and substrate turnover rates. | ||||||
5-Bromo-4-chloro-3-indolyl-α-L-fucopyranoside | 171869-92-4 | sc-284558 sc-284558A | 25 mg 50 mg | $226.00 $369.00 | ||
5-Bromo-4-chloro-3-indolyl-α-L-fucopyranoside serves as a substrate for fucosidases, exhibiting distinctive reactivity due to its halogenated indole structure. This compound's unique electronic properties promote selective interactions with enzyme active sites, influencing hydrolytic cleavage rates. Its ability to form stable enzyme-substrate complexes enhances reaction kinetics, while the presence of halogen substituents modulates steric effects, impacting substrate specificity and catalytic efficiency. | ||||||