| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sulbactam | 68373-14-8 | sc-272516 | 1 g | $80.00 | ||
Sulbactam acts as a potent beta-lactamase inhibitor, characterized by its ability to form covalent bonds with the active site serine residues of beta-lactamase enzymes. This interaction effectively blocks the hydrolysis of beta-lactam antibiotics, enhancing their stability. The compound's unique bicyclic structure allows for specific steric hindrance, which further impedes enzyme activity. Kinetic analyses demonstrate a competitive inhibition profile, highlighting its role in altering enzymatic reaction rates. | ||||||
Phenoxymethylpenilloic Acid | 4847-29-4 | sc-208165 | 10 mg | $300.00 | ||
Phenoxymethylpenilloic Acid functions as a beta-lactamase inhibitor through its ability to interact with the enzyme's active site, leading to the formation of stable acyl-enzyme complexes. This compound exhibits a distinctive structural configuration that enhances its affinity for beta-lactamase, effectively preventing substrate access. Its reaction kinetics reveal a non-competitive inhibition mechanism, showcasing its role in modulating enzymatic activity and prolonging the efficacy of beta-lactam antibiotics. | ||||||
3-(Acetylthio)-2-benzylpropionic Acid | 91702-98-6 | sc-209470 | 1 g | $220.00 | ||
3-(Acetylthio)-2-benzylpropionic Acid acts as a beta-lactamase inhibitor by forming covalent bonds with serine residues in the enzyme's active site, disrupting its catalytic function. The presence of the acetylthio group enhances its reactivity, allowing for rapid acylation and subsequent inactivation of the enzyme. This compound's unique steric and electronic properties facilitate selective binding, influencing the dynamics of enzyme-substrate interactions and altering the overall enzymatic pathway. | ||||||