Serotonin Activators
Santa Cruz Biotechnology now offers a broad range of Serotonin Activators. Serotonin (5-hydroxytryptamine, or 5-HT) is a monoamine neurotransmitter in the central nervous system (CNS) where serotonin is important in the regulation of mood, sleep, sexuality, and appetite. Low levels of serotonin are commonly associated with several disorders such as depression, migraines, bipolar disorder, and anxiety. Serotonin Activators offered by Santa Cruz activate Serotonin and, in some cases, other neurotransmitter and serotonin reuptake related proteins. View detailed Serotonin Activator specifications, including Serotonin Activator CAS number, molecular weight, molecular formula and chemical structure, by clicking on the product name.
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Items 1 to 10 of 25 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Nonyloxytryptamine oxalate | 157798-13-5 | sc-203480 sc-203480A | 10 mg 50 mg | $111.00 $627.00 | 2 | |
5-Nonyloxytryptamine oxalate is a synthetic derivative of serotonin, exhibiting unique interactions with serotonin receptors. Its elongated nonyl ether chain enhances lipophilicity, facilitating membrane penetration and receptor binding. This compound demonstrates distinct kinetic behavior, with a rapid onset of action that influences neurotransmitter release and synaptic plasticity. Additionally, its structural features may promote selective receptor activation, potentially leading to varied physiological responses. | ||||||
Fluoxetine | 54910-89-3 | sc-279166 | 500 mg | $312.00 | 9 | |
A selective serotonin reuptake inhibitor (SSRI), increases serotonin levels in the synaptic cleft. | ||||||
Xaliproden hydrochloride | 90494-79-4 | sc-203721 sc-203721A | 10 mg 50 mg | $224.00 $898.00 | ||
Xaliproden hydrochloride is a synthetic compound that modulates serotonin pathways through its unique structural configuration. The presence of a hydrochloride moiety enhances solubility, allowing for efficient interaction with serotonin receptors. Its specific molecular design promotes selective binding, influencing downstream signaling cascades. The compound exhibits notable stability in aqueous environments, which may affect its reactivity and interaction kinetics with biological targets, leading to diverse physiological implications. | ||||||
MK 212 hydrochloride | 64022-27-1 | sc-203634 sc-203634A | 10 mg 50 mg | $115.00 $473.00 | ||
MK 212 hydrochloride is a synthetic compound characterized by its ability to engage with serotonin receptors through a distinctive molecular architecture. The hydrochloride form enhances its ionic character, facilitating rapid diffusion across cellular membranes. This compound demonstrates a unique affinity for specific receptor subtypes, potentially altering neurotransmitter release dynamics. Its stability in various pH environments suggests a nuanced reactivity profile, influencing interaction rates and biological responses. | ||||||
Sertraline hydrochloride | 79559-97-0 | sc-201104 sc-201104A sc-201104B | 10 mg 50 mg 100 mg | $67.00 $102.00 $153.00 | 2 | |
Another SSRI, enhances serotonin activity by preventing its reuptake. | ||||||
Tandospirone hydrochloride | 99095-10-0 | sc-204320 sc-204320A | 10 mg 50 mg | $129.00 $548.00 | ||
Tandospirone hydrochloride is a synthetic compound notable for its selective interaction with serotonin receptors, exhibiting a unique binding affinity that influences receptor conformation. The hydrochloride form enhances solubility, promoting effective molecular interactions in aqueous environments. Its distinct pharmacokinetic profile allows for varied metabolic pathways, potentially modulating neurotransmitter systems. The compound's structural features contribute to its reactivity, impacting its overall biological behavior. | ||||||
Zacopride hydrochloride | 101303-98-4 | sc-203723 sc-203723A | 10 mg 50 mg | $137.00 $555.00 | ||
Zacopride hydrochloride is characterized by its intricate interactions with serotonin receptors, showcasing a unique affinity that alters receptor dynamics. The hydrochloride form increases its solubility, facilitating enhanced molecular interactions in biological systems. Its kinetic properties suggest a complex metabolic pathway, influencing neurotransmitter modulation. The compound's structural attributes play a crucial role in its reactivity, affecting its overall behavior in various environments. | ||||||
Paroxetine | 61869-08-7 | sc-507527 | 1 g | $180.00 | ||
SSRI that increases serotonin levels in the brain by inhibiting its reuptake into neurons. | ||||||
Ipsapirone | 95847-70-4 | sc-203607 sc-203607A | 10 mg 50 mg | $129.00 $525.00 | ||
Ipsapirone exhibits a distinctive profile in its interaction with serotonin receptors, particularly influencing the 5-HT1A subtype. Its unique structural features enable selective binding, which can modulate receptor conformations and downstream signaling pathways. The compound's hydrophilic characteristics enhance its solubility, promoting effective distribution in aqueous environments. Additionally, its dynamic molecular interactions suggest a nuanced role in neurotransmission, impacting synaptic plasticity and receptor sensitivity. | ||||||
Ro 60-0175 fumarate | 169675-09-6 | sc-204890 sc-204890A | 10 mg 50 mg | $145.00 $615.00 | ||
Ro 60-0175 fumarate demonstrates a unique affinity for serotonin receptors, particularly engaging with the 5-HT2A subtype. Its structural configuration allows for specific interactions that can alter receptor dynamics and influence intracellular signaling cascades. The compound's lipophilic nature facilitates membrane permeability, enhancing its ability to traverse lipid bilayers. Furthermore, its kinetic profile suggests rapid receptor binding and dissociation, contributing to its nuanced effects on serotonergic pathways. | ||||||