Aminopeptidase B Inhibitors
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Items 1 to 10 of 12 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Arphamenine B | 144110-38-3 | sc-202959 sc-202959A | 1 mg 5 mg | $39.00 $147.00 | ||
Arphamenine B functions as a selective inhibitor of Aminopeptidase B, exhibiting unique binding affinity that alters substrate specificity. Its molecular structure enables precise interactions with the enzyme's catalytic site, influencing the hydrolysis of basic amino acids. The compound's distinct steric properties enhance its interaction kinetics, allowing for a nuanced modulation of enzymatic activity. Additionally, its hydrophobic regions contribute to differential solubility, impacting its overall bioavailability in various environments. | ||||||
Bestatin | 58970-76-6 | sc-202975 | 10 mg | $128.00 | 19 | |
Bestatin acts as a potent inhibitor of Aminopeptidase B, characterized by its ability to form stable complexes with the enzyme. This interaction is facilitated by specific hydrogen bonding and hydrophobic contacts, which effectively disrupt the enzyme's catalytic function. The compound's unique stereochemistry allows for selective targeting of the enzyme's active site, influencing the kinetics of peptide hydrolysis. Furthermore, its solubility profile varies significantly, affecting its distribution in different biochemical contexts. | ||||||
Bestatin hydrochloride | 65391-42-6 | sc-200564 sc-200564A sc-200564B | 5 mg 25 mg 500 mg | $106.00 $352.00 $1132.00 | 1 | |
Bestatin hydrochloride is a selective inhibitor of Aminopeptidase B, showcasing a unique affinity for the enzyme's active site. Its structural conformation enables precise interactions, including van der Waals forces and electrostatic interactions, which modulate enzyme activity. The compound exhibits distinct reaction kinetics, altering substrate turnover rates. Additionally, its solubility characteristics can influence its behavior in various biochemical environments, impacting enzyme-substrate dynamics. | ||||||
Puromycin | 53-79-2 | sc-205821 sc-205821A | 10 mg 25 mg | $163.00 $316.00 | 436 | |
Inhibits protein synthesis by acting on ribosomes, reducing available substrates for Aminopeptidase B. | ||||||
CHR 2797 | 238750-77-1 | sc-285285 sc-285285A | 1 mg 10 mg | $119.00 $255.00 | ||
Cytoplasmic aminopeptidase inhibitor, impeding Aminopeptidase B′s peptide cleaving function. | ||||||
Amastatin hydrochloride | 100938-10-1 | sc-202051 sc-202051A | 1 mg 5 mg | $72.00 $214.00 | 3 | |
Aminopeptidase inhibitor that directly binds to the catalytic site of Aminopeptidase B. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Affects endosomal acidification, altering the intracellular environment in which Aminopeptidase B functions. | ||||||
Phosphoramidon | 119942-99-3 | sc-201283 sc-201283A | 5 mg 25 mg | $195.00 $620.00 | 8 | |
Metalloprotease inhibitor that can affect the catalytic activity of Aminopeptidase B. | ||||||
Phenylmethylsulfonyl Fluoride | 329-98-6 | sc-3597 sc-3597A | 1 g 100 g | $50.00 $683.00 | 92 | |
Serine protease inhibitor that affects the availability of peptide substrates for Aminopeptidase B. | ||||||
1,10-Phenanthroline | 66-71-7 | sc-255888 sc-255888A | 2.5 g 5 g | $23.00 $31.00 | ||
Metal-chelating agent that sequesters metal ions necessary for Aminopeptidase B activity. | ||||||