Date published: 2026-4-4

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β-glucuronidase Inhibitors

Santa Cruz Biotechnology now offers a broad range of beta-glucuronidase Inhibitors for use in various applications. Beta-glucuronidase inhibitors are a critical class of compounds in scientific research, particularly in the study of glycosaminoglycan metabolism and the breakdown of complex carbohydrates. Beta-glucuronidase is an enzyme responsible for hydrolyzing glucuronides, which are conjugates formed from glucuronic acid and various substrates, including drugs, hormones, and xenobiotics. This enzyme plays a crucial role in the degradation of glycosaminoglycans and the recycling of these molecules within lysosomes. By using beta-glucuronidase inhibitors, researchers can explore the enzyme's function in various biological processes, including cellular detoxification, the metabolism of endogenous compounds, and the regulation of inflammatory responses. These inhibitors are particularly valuable in studies aimed at understanding the enzyme's role in disease pathogenesis, especially in conditions where the accumulation of glycosaminoglycans or glucuronides is implicated, such as lysosomal storage disorders. Additionally, beta-glucuronidase inhibitors are employed in biochemical assays to investigate enzyme kinetics, substrate specificity, and the effects of potential regulatory molecules on enzyme activity. The availability of a diverse range of beta-glucuronidase inhibitors allows researchers to design experiments tailored to specific aspects of enzyme function, advancing our understanding of carbohydrate metabolism, cellular homeostasis, and the potential implications of altered enzyme activity in various biological systems. View detailed information on our available beta-glucuronidase Inhibitors by clicking on the product name.

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

D-saccharic acid calcium salt tetrahydrate

5793-89-5sc-205336
sc-205336A
25 g
100 g
$139.00
$373.00
1
(0)

D-saccharic acid calcium salt tetrahydrate acts as a potent beta-glucuronidase inhibitor through its ability to form stable complexes with the enzyme. Its unique structural features facilitate specific molecular interactions, disrupting the enzyme's active site and altering its catalytic pathway. The compound's tetrahydrate form enhances solubility, promoting effective binding dynamics. This interaction leads to a distinct modulation of reaction kinetics, influencing substrate turnover rates and enzyme activity profiles.