ST Inhibitors
Santa Cruz Biotechnology now offers a broad range of ST Inhibitors. Sodium-dependent serotonin transporter (ST) functions as a regulator of serotonergic signaling via transport of serotonin molecules from the synaptic cleft back into the pre-synaptic terminal for re-utilization. ST plays a key role in mediating regulation of the availability of serotonin to other receptors of serotonergic systems. ST Inhibitors offered by Santa Cruz inhibit ST and, in some cases, other neurotransmitter and serotonergic related proteins. View detailed ST Inhibitor specifications, including ST Inhibitor CAS number, molecular weight, molecular formula and chemical structure, by clicking on the product name.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Mesembrine | 24880-43-1 | sc-484336 sc-484336A sc-484336B sc-484336C sc-484336D | 1 mg 5 mg 10 mg 20 mg 50 mg | $316.00 $1270.00 $2086.00 $3718.00 $8165.00 | ||
Mesembrine exhibits intriguing properties as a natural alkaloid, characterized by its ability to modulate neurotransmitter systems through specific receptor interactions. Its stereochemistry contributes to unique binding affinities, influencing downstream signaling pathways. The compound's hydrophobic regions facilitate membrane permeability, while its polar functional groups enhance solubility in biological matrices. Additionally, Mesembrine's dynamic conformational landscape allows for versatile interactions with biomolecules, impacting its overall bioactivity. | ||||||
Pazopanib | 444731-52-6 | sc-396318 sc-396318A | 25 mg 50 mg | $127.00 $178.00 | 2 | |
Pazopanib, a receptor tyrosine kinase inhibitor, targets multiple signaling pathways. Its broad inhibitory effects can indirectly modulate ST, potentially impacting cellular processes associated with ST function and the signaling networks it intersects with. | ||||||
Vortioxetine Hydrobromide | 960203-27-4 | sc-475775 | 5 mg | $220.00 | ||
Vortioxetine Hydrobromide is a complex compound that showcases unique interactions with serotonin receptors, influencing various signaling cascades. Its distinct structural features allow for selective binding, which can modulate receptor activity. The presence of halogen atoms enhances its reactivity, facilitating specific molecular interactions. Additionally, the compound's amphiphilic nature promotes solubility in diverse environments, enabling it to traverse lipid membranes effectively. Its conformational flexibility further supports diverse interactions with target molecules. | ||||||