Nischarin Activators
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Clonidine hydrochloride | 4205-91-8 | sc-203002 | 1 g | $367.00 | 12 | |
Clonidine hydrochloride acts as a selective agonist at alpha-2 adrenergic receptors, facilitating unique molecular interactions that modulate neurotransmitter release. Its binding affinity influences downstream signaling pathways, particularly in the central nervous system. The compound exhibits distinct kinetic properties, affecting receptor desensitization and internalization. This results in altered synaptic transmission dynamics, contributing to its regulatory effects on neuronal excitability and vascular tone. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
An activator of protein kinase C (PKC), which can regulate cellular processes that intersect with Nischarin functions. | ||||||
Rilmenidine hemifumarate | 207572-68-7 | sc-203680 sc-203680A | 5 mg 25 mg | $110.00 $550.00 | ||
Rilmenidine hemifumarate functions as a selective agonist for imidazoline receptors, engaging in specific molecular interactions that influence intracellular signaling cascades. Its unique binding profile promotes the modulation of catecholamine release, impacting various physiological pathways. The compound's reaction kinetics reveal a distinct affinity for receptor subtypes, leading to differential activation patterns that affect cellular responses. This specificity enhances its role in regulating sympathetic nervous system activity. | ||||||
Naphazoline Hydrochloride | 550-99-2 | sc-205764 sc-205764A | 25 g 100 g | $49.00 $150.00 | ||
Naphazoline Hydrochloride acts as a potent vasoconstrictor through its interaction with alpha-adrenergic receptors, leading to localized effects on vascular smooth muscle. Its unique molecular structure facilitates rapid binding and dissociation kinetics, allowing for swift modulation of blood flow. The compound's hydrophilic properties enhance solubility, promoting effective diffusion across biological membranes. This behavior underscores its role in influencing vascular tone and permeability. | ||||||
Cimetidine | 51481-61-9 | sc-202996 sc-202996A | 5 g 10 g | $62.00 $86.00 | 1 | |
Cimetidine functions as a selective inhibitor of histamine H2 receptors, exhibiting unique molecular interactions that disrupt gastric acid secretion. Its structure allows for competitive binding, influencing downstream signaling pathways. The compound's ability to form hydrogen bonds enhances its affinity for target receptors, while its moderate lipophilicity aids in membrane permeability. This interplay of interactions contributes to its distinct pharmacokinetic profile, affecting absorption and distribution in various environments. | ||||||
Moxonidine hydrochloride | 75536-04-8 | sc-204096 sc-204096A | 10 mg 50 mg | $121.00 $495.00 | ||
Moxonidine hydrochloride acts as a selective modulator of imidazoline receptors, engaging in specific molecular interactions that influence neurotransmitter release. Its unique structure facilitates binding to these receptors, altering intracellular signaling cascades. The compound's capacity for forming ionic interactions enhances its stability in solution, while its distinct solubility characteristics affect its diffusion across biological membranes. This interplay of properties contributes to its unique kinetic behavior in various chemical environments. | ||||||