Santa Cruz Biotechnology now offers a broad range of SR-1A Inhibitors. SR-1A (Serotonin Receptor 1A), also known as 5-HT1A (5-hydroxytryptamine receptor 1A) is a subtype of 5-HT receptor that binds the endogenous neurotransmitter serotonin (5-hydroxytryptamine, 5-HT). The activity of SR-1A is mediated by G proteins that inhibit adenylate cyclase activity. SR-1A Inhibitors offered by Santa Cruz inhibit SR-1A and, in some cases, other adrenaline and adenylyl cyclase related proteins. View detailed SR-1A Inhibitor specifications, including SR-1A 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 |
|---|---|---|---|---|---|---|
Vortioxetine Hydrobromide | 960203-27-4 | sc-475775 | 5 mg | $220.00 | ||
Vortioxetine Hydrobromide, classified as an SR-1A compound, exhibits distinctive electrostatic interactions due to its halide component, which can influence solubility and reactivity in polar solvents. Its unique stereochemistry allows for selective binding to target sites, enhancing its interaction with other molecules. The compound's ability to form stable complexes through ionic and dipole-dipole interactions contributes to its kinetic profile, facilitating diverse reaction mechanisms in various chemical contexts. | ||||||
Pindolol-d7 | 1185031-19-9 | sc-219624 | 1 mg | $330.00 | ||
Pindolol-d7, an SR-1A compound, showcases intriguing isotopic labeling that alters its vibrational spectra, providing insights into molecular dynamics. Its unique hydrogen bonding capabilities enhance its reactivity, allowing for selective interactions with nucleophiles. The compound's distinct conformational flexibility influences its diffusion rates and reaction pathways, enabling it to participate in complex formation and catalysis under specific conditions, thus broadening its chemical versatility. | ||||||