Monoamine Oxidase Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Benserazide·HCl (Ro 4-4602) | 14919-77-8 | sc-200723 sc-200723A | 100 mg 1 g | $26.00 $85.00 | ||
Benserazide·HCl, a potent inhibitor of monoamine oxidase, showcases intriguing molecular interactions that modulate neurotransmitter levels. Its unique binding affinity alters enzyme kinetics, effectively slowing the degradation of monoamines. The compound's structural conformation allows for specific interactions with active sites, influencing reaction pathways. Additionally, its solubility characteristics enhance its reactivity in various biochemical environments, contributing to its distinct behavior in enzymatic processes. | ||||||
Phenelzine sulfate salt | 156-51-4 | sc-215701 | 5 g | $310.00 | 3 | |
Phenelzine sulfate salt acts as a selective monoamine oxidase inhibitor, exhibiting unique interactions with the enzyme's active site. Its structural features facilitate the formation of stable enzyme-inhibitor complexes, significantly impacting the catalytic efficiency of monoamine degradation. The compound's ability to alter electron distribution enhances its reactivity, while its solubility profile allows for effective diffusion in biological systems, influencing metabolic pathways and reaction dynamics. | ||||||
R(−)-Deprenyl hydrochloride | 14611-52-0 | sc-200742 sc-200742A sc-200742B | 100 mg 250 mg 1 g | $32.00 $77.00 $281.00 | ||
R(-)-Deprenyl hydrochloride functions as a selective monoamine oxidase inhibitor, characterized by its unique binding affinity to the enzyme's flavin cofactor. This interaction stabilizes the enzyme's conformation, leading to altered reaction kinetics and reduced substrate turnover. The compound's stereochemistry contributes to its specificity, while its lipophilic nature enhances membrane permeability, facilitating its engagement in neurochemical pathways and modulating neurotransmitter levels. | ||||||
Clorgyline hydrochloride | 17780-75-5 | sc-214749 sc-214749A | 50 mg 100 mg | $125.00 $210.00 | 2 | |
Clorgyline hydrochloride acts as a selective monoamine oxidase inhibitor, exhibiting a strong affinity for the enzyme's active site. Its unique structural features allow for specific interactions with the enzyme's flavin adenine dinucleotide (FAD) cofactor, effectively hindering the oxidative deamination of neurotransmitters. This inhibition alters metabolic pathways, resulting in a distinctive modulation of monoamine levels, while its hydrophobic characteristics promote effective cellular uptake and distribution. | ||||||
S(-)-Carbidopa | 38821-49-7 | sc-361978 | 5 g | $500.00 | ||
S(-)-Carbidopa functions as a monoamine oxidase inhibitor by selectively binding to the enzyme's active site, disrupting its catalytic activity. Its stereochemistry enhances interactions with the enzyme's binding pocket, leading to altered reaction kinetics and a reduction in the breakdown of key neurotransmitters. This compound's unique conformation facilitates specific molecular interactions, influencing metabolic pathways and contributing to its distinct biochemical profile. | ||||||
Ro 16-6491 | 94319-79-6 | sc-200743 sc-200743A | 200 mg 1 g | $57.00 $218.00 | ||
Ro 16-6491 acts as a monoamine oxidase inhibitor through its ability to form stable complexes with the enzyme, effectively hindering its function. The compound's unique structural features allow for selective interactions with the enzyme's active site, modulating the kinetics of neurotransmitter degradation. This selective binding alters the enzyme's conformational dynamics, impacting various metabolic pathways and enhancing the stability of certain biogenic amines within the system. | ||||||
Rasagiline | 136236-51-6 | sc-204875 sc-204875A | 25 mg 100 mg | $101.00 $210.00 | ||
Rasagiline functions as a monoamine oxidase inhibitor by engaging in specific non-covalent interactions with the enzyme, leading to a reduction in its catalytic activity. Its unique molecular architecture facilitates preferential binding to the enzyme's active site, influencing the reaction kinetics of neurotransmitter metabolism. This interaction not only stabilizes the enzyme's conformation but also affects the turnover rates of various substrates, thereby modulating biochemical pathways associated with amine regulation. | ||||||
Pimprinine | 13640-26-1 | sc-202288 | 1 mg | $291.00 | ||
Pimprinine acts as a monoamine oxidase by selectively interacting with the enzyme's active site, altering its conformational dynamics. This compound exhibits unique binding affinities that influence the enzyme's substrate specificity and catalytic efficiency. Its structural features promote distinct electron transfer mechanisms, impacting the degradation pathways of biogenic amines. Additionally, Pimprinine's presence can modulate the redox state of the enzyme, further affecting neurotransmitter homeostasis. | ||||||
2-Propynal | 624-67-9 | sc-344980 | 1 g | $400.00 | ||
2-Propynal functions as a monoamine oxidase by engaging in specific interactions with the enzyme's active site, leading to alterations in its catalytic behavior. Its unique carbonyl group facilitates the formation of transient intermediates, enhancing reaction kinetics. The compound's steric properties influence substrate accessibility, while its electron-withdrawing characteristics can stabilize charged transition states, ultimately affecting the metabolic pathways of amines. | ||||||
Ethyl homovanillate | 60563-13-5 | sc-235050 | 1 g | $54.00 | ||
Ethyl homovanillate acts as a monoamine oxidase by selectively binding to the enzyme's active site, promoting conformational changes that modulate its activity. The presence of the methoxy and hydroxyl groups enhances hydrogen bonding interactions, which can stabilize enzyme-substrate complexes. Additionally, its aromatic structure contributes to unique π-π stacking interactions, influencing the enzyme's substrate specificity and altering the dynamics of amine metabolism. | ||||||