MAO-B Inhibitors
Items 21 to 25 of 25 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Nialamide | 51-12-7 | sc-253186 | 1 g | $98.00 | ||
Nialamide functions as a selective MAO-B inhibitor, distinguished by its unique aromatic amine structure that allows for specific π-π stacking interactions with the enzyme's active site. The presence of nitrogen atoms contributes to hydrogen bonding, enhancing binding stability. Its electron-rich framework can modulate the enzyme's redox state, potentially influencing reaction kinetics and substrate availability, thereby impacting metabolic pathways in a nuanced manner. | ||||||
Isatin | 91-56-5 | sc-205721 sc-205721A | 100 g 500 g | $63.00 $276.00 | ||
Isatin exhibits notable interactions as a MAO-B inhibitor, characterized by its ability to form strong hydrogen bonds due to its carbonyl and nitrogen functionalities. This compound can engage in hydrophobic interactions with the enzyme, promoting a stable binding conformation. Its planar structure facilitates π-π interactions, which may alter the enzyme's conformation and affect substrate affinity, ultimately influencing the catalytic efficiency and metabolic dynamics within the system. | ||||||
trans 2-(Phenyl-d5)-cyclopropylamine Hydrochloride | 107077-98-5 | sc-220292 | 1 mg | $290.00 | ||
Trans 2-(Phenyl-d5)-cyclopropylamine Hydrochloride demonstrates intriguing behavior as a MAO-B inhibitor through its unique cyclopropyl structure, which introduces ring strain that can enhance binding affinity. The presence of deuterated phenyl groups allows for distinct isotopic effects, potentially influencing reaction kinetics. Its ability to engage in both steric and electronic interactions with the enzyme's active site may modulate conformational dynamics, impacting overall enzymatic activity and substrate processing. | ||||||
Bifemelane hydrochloride | 62232-46-6 | sc-203529 sc-203529A | 10 mg 50 mg | $280.00 $800.00 | ||
Bifemelane hydrochloride exhibits notable characteristics as a MAO-B inhibitor, primarily due to its unique structural features that facilitate selective enzyme interaction. The compound's specific functional groups enable it to form stable hydrogen bonds and hydrophobic interactions within the active site, enhancing its binding efficiency. Additionally, its stereochemistry may influence the enzyme's conformational flexibility, potentially altering substrate accessibility and catalytic efficiency in metabolic pathways. | ||||||
Rasagiline-13C3 Mesylate | 1391052-18-8 | sc-477172 sc-477172A | 1 mg 10 mg | $410.00 $3000.00 | ||
Rasagiline-13C3 Mesylate is characterized by its stable isotopic labeling, which allows for precise tracking in metabolic studies. Its unique structure facilitates specific interactions with MAO-B, enhancing selectivity in enzyme binding. The compound's kinetic profile reveals a rapid onset of inhibition, influenced by its conformational flexibility. Additionally, the presence of the mesylate group contributes to its solubility and reactivity, impacting its behavior in various chemical environments. | ||||||