| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(2S)-(+)-Amino-5-iodoacetamidopentanoic acid | 35748-65-3 | sc-202409 sc-202409A | 5 mg 25 mg | $209.00 $413.00 | ||
(2S)-(+)-Amino-5-iodoacetamidopentanoic acid functions as a selective arginase inhibitor, characterized by its ability to form specific ionic interactions with key residues in the enzyme's active site. This compound stabilizes a unique conformation of arginase, effectively modulating its catalytic efficiency. Its structural features promote distinct conformational shifts, impacting substrate binding and turnover rates, while its solubility profile allows for effective integration into various biochemical assays. | ||||||
NG-Hydroxy-L-arginine, Monoacetate Salt | 53598-01-9 | sc-222067A sc-222067 | 5 mg 25 mg | $109.00 $395.00 | ||
NG-Hydroxy-L-arginine, Monoacetate Salt acts as an arginase modulator, exhibiting unique binding dynamics that influence enzyme activity. Its hydroxyl group facilitates hydrogen bonding with critical amino acids in the active site, enhancing substrate affinity. This compound also alters the enzyme's conformational landscape, leading to variations in reaction kinetics. Additionally, its acetate moiety contributes to solubility, enabling diverse interactions in biochemical environments. | ||||||
(2S)-(+)-Amino-6-iodoacetamidohexanoic acid | 90764-56-0 | sc-220847 | 5 mg | $204.00 | ||
(2S)-(+)-Amino-6-iodoacetamidohexanoic acid functions as an arginase inhibitor, characterized by its ability to form stable complexes with the enzyme's active site. The presence of the iodoacetamido group introduces steric hindrance, which modulates substrate access and alters catalytic efficiency. This compound's unique structural features promote specific electrostatic interactions, influencing the enzyme's conformational stability and overall reactivity in metabolic pathways. | ||||||