Date published: 2025-10-7

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beta-glucosidase Inhibitors

Santa Cruz Biotechnology now offers a broad range of beta-glucosidase Inhibitors for use in various applications. Beta-glucosidase inhibitors are a vital category of compounds in scientific research, particularly in the study of carbohydrate metabolism and the breakdown of glycosidic bonds. Beta-glucosidase is an enzyme that catalyzes the hydrolysis of beta-glucosides into glucose and other components, playing a crucial role in the degradation of complex carbohydrates and glycosides. By inhibiting this enzyme, researchers can explore the mechanisms of carbohydrate digestion and the broader implications of glycosidase activity in various biological systems. Beta-glucosidase inhibitors are especially valuable in studies aimed at understanding the regulation of glucose release from stored glycogen and plant biomass, providing insights into metabolic pathways that are essential for energy production and storage. These inhibitors are also employed in research focused on the role of glycosidases in plant physiology, where they help dissect the processes of cellulose degradation and lignocellulosic biomass conversion, which are critical for biofuel production and agricultural applications. Additionally, beta-glucosidase inhibitors are used in enzyme kinetics studies to explore the specificity and efficiency of enzyme-substrate interactions, contributing to the development of new strategies for modulating enzyme activity in various industrial and biotechnological processes. The availability of a diverse range of beta-glucosidase inhibitors allows researchers to design experiments tailored to specific aspects of carbohydrate metabolism and enzyme function, advancing our understanding of these fundamental biological processes. View detailed information on our available beta-glucosidase Inhibitors by clicking on the product name.

Items 1 to 10 of 15 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Isofagomine D-Tartrate

957230-65-8sc-207767
sc-207767A
sc-207767C
sc-207767B
5 mg
10 mg
50 mg
25 mg
$379.00
$710.00
$1975.00
$1199.00
(1)

Isofagomine D-Tartrate acts as a selective beta-glucosidase inhibitor, characterized by its ability to mimic the transition state of substrate binding. This compound exhibits unique interactions with the enzyme's active site, stabilizing the transition state and effectively slowing down the hydrolysis of glycosidic bonds. Its specific stereochemical arrangement enhances binding affinity, influencing reaction kinetics and providing a deeper understanding of enzyme mechanisms in carbohydrate processing.

Conduritol B Epoxide (CBE)

6090-95-5sc-201356
sc-201356A
sc-201356B
sc-201356C
sc-201356D
sc-201356E
sc-201356F
5 mg
25 mg
50 mg
100 mg
250 mg
1 g
5 g
$76.00
$270.00
$490.00
$614.00
$1285.00
$5110.00
$20410.00
12
(1)

Conduritol B Epoxide (CBE) serves as a potent beta-glucosidase inhibitor, distinguished by its ability to form covalent bonds with the enzyme's active site. This irreversible binding alters the enzyme's conformation, leading to a significant reduction in catalytic activity. The epoxide group facilitates unique electrophilic interactions, enhancing specificity and selectivity. CBE's structural features contribute to its unique reactivity, providing insights into enzyme regulation and carbohydrate metabolism pathways.

Acarbose

56180-94-0sc-203492
sc-203492A
1 g
5 g
$222.00
$593.00
1
(1)

Acarbose inhibits alpha-glucosidase enzymes, including beta-glucosidases.

Castanospermine

79831-76-8sc-201358
sc-201358A
100 mg
500 mg
$180.00
$620.00
10
(1)

Castanospermine is a notable beta-glucosidase inhibitor characterized by its ability to interact with the enzyme through non-covalent interactions, particularly hydrogen bonding and hydrophobic effects. This interaction stabilizes a specific enzyme conformation, effectively modulating its activity. The compound's unique stereochemistry influences its binding affinity, allowing for selective inhibition. Additionally, its presence can alter substrate accessibility, providing insights into glycosidic bond hydrolysis mechanisms and carbohydrate processing pathways.

Miglitol

72432-03-2sc-221943
10 mg
$158.00
1
(1)

Miglitol works by inhibiting alpha-glucosidases, including beta-glucosidase.

Deoxynojirimycin

19130-96-2sc-201369
sc-201369A
1 mg
5 mg
$72.00
$142.00
(0)

Deoxynojirimycin functions as a beta-glucosidase inhibitor by mimicking the natural substrate, facilitating competitive inhibition. Its structural conformation allows for effective binding to the enzyme's active site, disrupting normal catalytic activity. The compound's unique hydroxyl groups enhance its solubility and interaction with the enzyme, influencing reaction kinetics. This modulation of enzyme dynamics offers a deeper understanding of glycosidic bond interactions and carbohydrate metabolism.

Conduritol B

25348-64-5sc-207453
25 mg
$268.00
(0)

Conduritol B acts as a beta-glucosidase inhibitor through its structural similarity to glucose, allowing it to effectively occupy the enzyme's active site. Its distinctive bicyclic structure promotes specific molecular interactions that stabilize the enzyme-inhibitor complex, altering the reaction kinetics. This compound's ability to influence the hydrolysis of glycosidic bonds provides insights into carbohydrate processing and enzyme regulation, highlighting its role in glycoside metabolism.

Quercetin

117-39-5sc-206089
sc-206089A
sc-206089E
sc-206089C
sc-206089D
sc-206089B
100 mg
500 mg
100 g
250 g
1 kg
25 g
$11.00
$17.00
$108.00
$245.00
$918.00
$49.00
33
(2)

Quercetin is a flavonoid found in various fruits and vegetables. It has been shown to inhibit beta-glucosidase activity.

1-Deoxynojirimycin Hydrochloride

73285-50-4sc-201694
sc-201694A
sc-201694B
1 mg
10 mg
100 mg
$73.00
$150.00
$420.00
2
(0)

1-Deoxynojirimycin Hydrochloride functions as a beta-glucosidase inhibitor by mimicking the substrate's conformation, enabling it to bind effectively to the enzyme's active site. Its unique pyrrolidine ring structure enhances its affinity for the enzyme, leading to altered catalytic efficiency. This compound's interactions can modulate glycosidic bond hydrolysis, offering a deeper understanding of enzyme dynamics and carbohydrate metabolism pathways.

O-(D-Glucopyranosylidene)amino N-Phenylcarbamate

104012-84-2sc-208112
10 mg
$274.00
(0)

O-(D-Glucopyranosylidene)amino N-Phenylcarbamate acts as a beta-glucosidase by engaging in specific hydrogen bonding and hydrophobic interactions with the enzyme's active site. Its glucopyranosylidene moiety facilitates substrate recognition, while the phenylcarbamate group enhances stability and specificity. This compound's kinetic profile reveals a unique mechanism of action, influencing the rate of glycosidic bond cleavage and providing insights into carbohydrate enzymology.