MAO-A Inhibitors
Items 1 to 10 of 24 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Quinacrine, Dihydrochloride | 69-05-6 | sc-204222 sc-204222B sc-204222A sc-204222C sc-204222D | 100 mg 1 g 5 g 200 g 300 g | $45.00 $56.00 $85.00 $3193.00 $4726.00 | 4 | |
Quinacrine, Dihydrochloride acts as a monoamine oxidase A (MAO-A) inhibitor by forming specific interactions with the enzyme's active site. Its unique aromatic structure allows for π-π stacking and van der Waals forces, facilitating a stable binding conformation. This compound also influences the enzyme's catalytic efficiency by altering the electron distribution within its molecular framework, thereby affecting substrate accessibility and reaction dynamics. | ||||||
Pirlindole mesylate | 60762-57-4 | sc-203664 sc-203664A | 10 mg 50 mg | $149.00 $617.00 | 2 | |
Pirlindole mesylate functions as a monoamine oxidase A (MAO-A) inhibitor through its distinctive molecular architecture, which promotes hydrophobic interactions and hydrogen bonding with the enzyme. This compound's ability to modulate the enzyme's conformational dynamics enhances its binding affinity, leading to altered kinetic parameters. Additionally, its specific stereochemistry may influence the spatial orientation of substrates, further impacting enzymatic activity and metabolic pathways. | ||||||
cis-Resveratrol Solution (in Ethanol) | 61434-67-1 | sc-205254 sc-205254A | 5 mg 10 mg | $120.00 $228.00 | 2 | |
Cis-Resveratrol Solution in Ethanol exhibits unique interactions with monoamine oxidase A (MAO-A) due to its planar structure and hydroxyl groups, which facilitate strong hydrogen bonding and π-π stacking with the enzyme. This compound's ability to stabilize enzyme-substrate complexes alters reaction kinetics, enhancing selectivity. Its solubility in ethanol allows for effective diffusion, potentially influencing the enzyme's local microenvironment and catalytic efficiency. | ||||||
Quinacrine Dihydrochloride Dihydrate | 6151-30-0 | sc-391946B sc-391946C sc-391946 sc-391946A | 1 g 5 g 10 g 25 g | $42.00 $84.00 $161.00 $338.00 | 1 | |
Quinacrine Dihydrochloride Dihydrate demonstrates intriguing interactions with monoamine oxidase A (MAO-A) through its unique heterocyclic structure, which allows for specific electrostatic interactions and conformational flexibility. This compound can modulate the enzyme's active site dynamics, potentially affecting substrate accessibility and turnover rates. Its crystalline form contributes to stability, while its hydrophilic nature enhances solubility in aqueous environments, influencing its reactivity and interaction profiles. | ||||||
Harmine | 442-51-3 | sc-202644 sc-202644A sc-202644B sc-202644C sc-202644D sc-202644E sc-202644F | 250 mg 500 mg 1 g 10 g 50 g 100 g 500 g | $52.00 $102.00 $124.00 $540.00 $1438.00 $2560.00 $11230.00 | 2 | |
Harmine demonstrates a unique affinity for monoamine oxidase A (MAO-A) through its intricate molecular structure, which allows for specific interactions at the enzyme's active site. The compound's planar configuration enables π-π stacking with aromatic residues, enhancing binding stability. Furthermore, its capacity to engage in electrostatic interactions can modulate enzyme activity, while its lipophilic characteristics facilitate membrane permeability, influencing its kinetic profile in metabolic pathways. | ||||||
Bifemelane hydrochloride | 62232-46-6 | sc-203529 sc-203529A | 10 mg 50 mg | $280.00 $800.00 | ||
Bifemelane hydrochloride exhibits distinctive interactions with monoamine oxidase A (MAO-A) due to its unique structural features, which facilitate selective binding to the enzyme's active site. This compound's ability to form hydrogen bonds and hydrophobic interactions can alter the enzyme's conformation, impacting its catalytic efficiency. Additionally, its ionic nature enhances solubility, promoting effective diffusion in biological systems and influencing its kinetic behavior in enzymatic reactions. | ||||||
trans 2-Phenylcyclopropylamine Hydrochloride | 1986-47-6 | sc-208452 sc-208452A | 250 mg 1 g | $56.00 $163.00 | 1 | |
Trans 2-Phenylcyclopropylamine Hydrochloride exhibits a distinctive interaction with monoamine oxidase A (MAO-A) due to its cyclopropyl moiety, which introduces strain and flexibility in the molecular framework. This strain enhances the compound's ability to fit into the enzyme's active site, promoting effective binding. Additionally, the presence of the phenyl group allows for hydrophobic interactions, potentially influencing the enzyme's conformational dynamics and reaction kinetics, thereby affecting substrate turnover rates. | ||||||
Isocarboxazid | 59-63-2 | sc-218606 | 100 mg | $330.00 | 1 | |
Isocarboxazid is a non-selective, irreversible MAO inhibitor. It forms a covalent bond with the enzyme′s active site, blocking the breakdown of various monoamine neurotransmitters. | ||||||
Coptisin chloride | 6020-18-4 | sc-281638 | 10 mg | $459.00 | ||
Coptisin chloride demonstrates a unique affinity for monoamine oxidase A (MAO-A) through its specific structural features, which facilitate strong electrostatic interactions with the enzyme's active site. The presence of halogen atoms enhances its reactivity, allowing for rapid formation of enzyme-inhibitor complexes. This compound's distinct electronic properties may also modulate the enzyme's catalytic efficiency, influencing the overall metabolic pathways of monoamines. | ||||||
cis-Resveratrol | 61434-67-1 | sc-363863 sc-363863A | 10 mg 100 mg | $340.00 $2400.00 | 2 | |
Cis-Resveratrol exhibits intriguing interactions with monoamine oxidase A (MAO-A) due to its planar structure, which allows for effective π-π stacking with aromatic residues in the enzyme's active site. This compound's hydroxyl groups can form hydrogen bonds, stabilizing the enzyme-inhibitor complex. Additionally, its stereochemistry may influence binding kinetics, potentially altering the enzyme's conformational dynamics and affecting monoamine degradation pathways. | ||||||