beta-glucosidase Substrates
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4-Methylumbelliferyl-β-D-glucopyranoside | 18997-57-4 | sc-280455 sc-280455A sc-280455B sc-280455C | 1 g 5 g 25 g 100 g | $153.00 $265.00 $459.00 $1758.00 | ||
4-Methylumbelliferyl-β-D-glucopyranoside acts as a beta-glucosidase substrate, characterized by its fluorescent properties that facilitate real-time monitoring of enzymatic activity. The compound's glucopyranoside moiety enhances its affinity for the enzyme, promoting effective hydrolysis. Its unique structure allows for specific interactions with active site residues, influencing reaction rates and providing insights into glycosidic bond cleavage mechanisms in carbohydrate biochemistry. | ||||||
D-Cellobiose | 528-50-7 | sc-280654 sc-280654A | 5 g 25 g | $45.00 $110.00 | 1 | |
D-Cellobiose serves as a substrate for beta-glucosidase, featuring a disaccharide structure that promotes specific enzyme interactions. Its unique configuration allows for efficient binding at the active site, enhancing hydrolytic activity. The compound's dual glucose units facilitate distinct reaction pathways, influencing kinetic parameters such as turnover number and substrate affinity. This specificity aids in elucidating the mechanisms of cellulose degradation and carbohydrate metabolism. | ||||||
Linamarin | 554-35-8 | sc-203439 | 50 mg | $262.00 | 5 | |
Linamarin is a cyanogenic glycoside that acts as a substrate for beta-glucosidase, showcasing a unique structural arrangement that enables selective enzyme recognition. Its specific glycosidic bond configuration allows for effective hydrolysis, leading to the release of glucose and toxic hydrogen cyanide. The compound's reactivity is influenced by its stereochemistry, which affects the enzyme's catalytic efficiency and reaction kinetics, providing insights into plant defense mechanisms and metabolic pathways. | ||||||
4-Nitrophenyl-β-D- glucopyranoside | 2492-87-7 | sc-281429 sc-281429A sc-281429B sc-281429C | 2 g 5 g 25 g 100 g | $194.00 $219.00 $520.00 $1846.00 | ||
4-Nitrophenyl-β-D-glucopyranoside serves as a substrate for beta-glucosidase, characterized by its nitrophenyl group that enhances the compound's electrophilicity. This unique feature facilitates the enzyme's hydrolytic activity, resulting in the release of glucose and a nitrophenol byproduct. The compound's structural properties influence the enzyme's binding affinity and catalytic turnover, offering insights into glycosidic bond cleavage mechanisms and enzyme specificity in carbohydrate metabolism. | ||||||
5-Bromo-4-chloro-3-indolyl β-D-glucopyranoside | 15548-60-4 | sc-221009 sc-221009A | 5 mg 25 mg | $151.00 $491.00 | ||
5-Bromo-4-chloro-3-indolyl β-D-glucopyranoside acts as a substrate for beta-glucosidase, distinguished by its indolyl moiety that contributes to unique steric and electronic properties. This structure enhances enzyme-substrate interactions, promoting efficient hydrolysis. The compound's specific configuration influences reaction kinetics, allowing for detailed studies of glycosidic bond dynamics and enzyme selectivity in carbohydrate processing, revealing intricate pathways of enzymatic catalysis. | ||||||
D-(−)-Salicin | 138-52-3 | sc-218004 | 5 g | $58.00 | ||
D-(-)-Salicin serves as a substrate for beta-glucosidase, characterized by its phenolic structure that facilitates hydrogen bonding and hydrophobic interactions with the enzyme's active site. This interaction enhances the enzyme's catalytic efficiency, leading to rapid hydrolysis of glycosidic bonds. The compound's stereochemistry plays a crucial role in modulating reaction rates, providing insights into the specificity and mechanisms of glycosidic bond cleavage in carbohydrate metabolism. | ||||||
4-(Trifluoromethyl)umbelliferyl-β-D-glucopyranoside | 116981-86-3 | sc-220918 sc-220918A | 5 mg 10 mg | $190.00 $340.00 | ||
4-(Trifluoromethyl)umbelliferyl-β-D-glucopyranoside acts as a substrate for beta-glucosidase, featuring a unique trifluoromethyl group that influences electronic properties and steric hindrance. This modification enhances the compound's affinity for the enzyme, promoting effective substrate binding. The umbelliferone moiety contributes to fluorescence, allowing for real-time monitoring of enzymatic activity. Its distinct structural characteristics facilitate insights into enzyme kinetics and substrate specificity in glycoside hydrolysis. | ||||||
Naphthol AS-BI β-D-galactopyranoside | 51349-63-4 | sc-222039 sc-222039A | 250 mg 2 g | $228.00 $587.00 | ||
Naphthol AS-BI β-D-galactopyranoside serves as a substrate for beta-glucosidase, characterized by its naphthol structure that enhances hydrophobic interactions with the enzyme. This compound exhibits unique reaction kinetics, with a notable rate of hydrolysis influenced by its glycosidic bond configuration. The presence of the β-D-galactopyranoside moiety allows for selective enzyme recognition, providing insights into substrate specificity and catalytic efficiency in glycosidic bond cleavage. | ||||||