Aminopeptidase Inhibitors
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Actinonin | 13434-13-4 | sc-201289 sc-201289B | 5 mg 10 mg | $170.00 $385.00 | 3 | |
Actinonin is a potent inhibitor of aminopeptidases, distinguished by its ability to form stable complexes with the enzyme's active site. This interaction alters the enzyme's conformation, significantly impacting substrate accessibility and reaction rates. The compound's unique structural motifs facilitate specific hydrogen bonding and hydrophobic interactions, enhancing its binding affinity. As a result, Actinonin effectively modulates enzymatic activity, providing insights into amino acid metabolism pathways. | ||||||
CHR 2797 | 238750-77-1 | sc-285285 sc-285285A | 1 mg 10 mg | $119.00 $255.00 | ||
CHR 2797 exhibits remarkable selectivity as an aminopeptidase inhibitor, characterized by its unique ability to disrupt enzyme-substrate interactions through competitive inhibition. Its structural features promote specific electrostatic interactions, which stabilize the enzyme's transition state. This compound influences reaction kinetics by altering the activation energy required for substrate cleavage, thereby providing a nuanced understanding of proteolytic pathways and enzyme regulation. | ||||||
Ebelactone A | 76808-16-7 | sc-203035 | 1 mg | $98.00 | ||
Ebelactone A functions as a potent aminopeptidase, showcasing a distinctive mechanism of action through its ability to modulate enzyme activity via allosteric sites. Its unique stereochemistry facilitates specific binding interactions that enhance substrate affinity, leading to altered catalytic efficiency. The compound's influence on enzyme conformational dynamics provides insights into proteolytic regulation, revealing intricate pathways of amino acid processing and metabolic control. | ||||||
Bestatin Methyl Ester | 65322-89-6 | sc-221350 | 5 mg | $218.00 | 2 | |
Bestatin Methyl Ester acts as a selective aminopeptidase inhibitor, characterized by its ability to form stable complexes with the enzyme's active site. This interaction disrupts substrate access, effectively modulating enzymatic activity. Its unique structural features promote specific hydrogen bonding and hydrophobic interactions, influencing reaction kinetics. The compound's role in altering enzyme stability and dynamics offers a deeper understanding of proteolytic mechanisms and amino acid metabolism. | ||||||
L-Glutamic acid γ-(7-amido-4-methylcoumarin) | 72669-53-5 | sc-281542 sc-281542A | 50 mg 100 mg | $157.00 $221.00 | ||
L-Glutamic acid γ-(7-amido-4-methylcoumarin) serves as a potent substrate for aminopeptidases, showcasing a distinctive fluorescence upon enzymatic cleavage. This property allows for real-time monitoring of enzymatic activity. The compound's structural design facilitates specific interactions with the enzyme's active site, enhancing substrate affinity and influencing catalytic efficiency. Its unique coumarin moiety contributes to the modulation of reaction pathways, providing insights into enzyme kinetics and substrate specificity. | ||||||
Epiamastatin hydrochloride | 100992-59-4 | sc-214965 | 5 mg | $1764.00 | ||
Epiamastatin hydrochloride acts as a selective inhibitor of aminopeptidases, characterized by its ability to form stable complexes with the enzyme's active site. This interaction alters the enzyme's conformation, effectively modulating its catalytic activity. The compound's unique structural features promote specific binding, influencing reaction rates and substrate turnover. Its distinct kinetic profile allows for detailed studies of enzyme mechanisms and regulatory pathways, enhancing our understanding of proteolytic processes. | ||||||