Date published: 2026-4-24

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FUCA Inhibitors

Santa Cruz Biotechnology now offers a broad range of FUCA Inhibitors for use in various applications. FUCA Inhibitors are specialized compounds that target α-L-fucosidase (FUCA), an enzyme involved in the hydrolysis of fucose-containing glycoconjugates. These inhibitors are vital tools in biochemical and molecular biology research, particularly for studying the roles of fucosylation in cellular processes. By inhibiting FUCA, researchers can explore the regulatory mechanisms governing the metabolism and function of fucose residues in glycoproteins, glycolipids, and other glycoconjugates. This research is crucial for understanding how fucosylation affects cellular signaling, adhesion, and communication. FUCA Inhibitors enable scientists to dissect the pathways of glycan processing and modification, providing insights into how these modifications influence protein folding, stability, and interactions. In experimental settings, FUCA Inhibitors allow for precise control over enzyme activity, facilitating detailed studies of substrate specificity, enzyme kinetics, and the broader implications of altered fucosylation on cellular functions. These inhibitors are also valuable in glycomics and structural biology, helping to study the three-dimensional structures of fucosylated molecules and their complexes. By using FUCA Inhibitors, researchers can map out the functional roles of fucose in various biological systems, contributing to a comprehensive understanding of cellular metabolism and its regulation. Furthermore, these inhibitors are essential for developing assays to measure α-L-fucosidase activity and to screen for potential modulators of this enzyme. FUCA Inhibitors thus serve as indispensable tools for researchers aiming to uncover the complexities of glycan biology and the regulatory networks that maintain cellular homeostasis. View detailed information on our available FUCA Inhibitors by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Deoxyfuconojirimycin hydrochloride

210174-73-5sc-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
(0)

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

171869-92-4sc-284558
sc-284558A
25 mg
50 mg
$226.00
$369.00
(0)

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.