Date published: 2025-11-22

1-800-457-3801

SCBT Portrait Logo
Seach Input

SR-3B Inhibitors

Serotonin is a neurotransmitter found in serotonergic neurons in the central nervous system and enterochromaffin cells in the gastrointestinal tract. Biochemicals that inhibit SR-3B have many applications in biochemical and physiological research. SR-3B inhibitors belong to a specific chemical class that has garnered significant attention in scientific research. These inhibitors are designed to target and modulate the activity of a particular protein known as SR-3B. The chemical structure of SR-3B inhibitors consists of a unique arrangement of atoms, which enables them to bind specifically to the active site of the SR-3B protein. This binding interaction between the inhibitors and the protein results in the inhibition of SR-3B's enzymatic function. The precise mechanism by which SR-3B inhibitors achieve this inhibition is still an active area of investigation. The development of SR-3B inhibitors has been driven by the desire to understand the biological role of SR-3B and its implications in various cellular processes. Researchers have extensively studied the structure-activity relationships of these inhibitors to optimize their potency, selectivity, and properties. The aim is to design inhibitors that can effectively interact with SR-3B, thereby modulating its activity without causing significant interference with other cellular processes. Studies focusing on SR-3B inhibitors have provided valuable insights into the function and regulation of SR-3B in cellular contexts. By selectively inhibiting SR-3B, researchers can probe its role in specific pathways or cellular functions, leading to a better understanding of its involvement in physiological and pathological processes.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

SDZ 205-557 hydrochloride

137196-67-9sc-204273
sc-204273A
10 mg
50 mg
$119.00
$510.00
(0)

SDZ 205-557 hydrochloride, classified as an SR-3B compound, showcases remarkable solubility characteristics that enhance its interaction with polar solvents. Its unique steric configuration promotes specific hydrogen bonding patterns, influencing its reactivity in nucleophilic substitution reactions. Additionally, the compound's ability to form stable complexes with metal ions highlights its potential for diverse coordination chemistry, while its distinct electronic properties facilitate intriguing photophysical behaviors.

3-AQC

sc-203776
sc-203776A
5 mg
25 mg
$96.00
$381.00
(0)

3-AQC, an SR-3B compound, exhibits intriguing reactivity as an acid halide, characterized by its propensity for rapid acylation reactions. Its unique electronic structure allows for selective electrophilic interactions, enhancing its reactivity with nucleophiles. The compound's distinct steric hindrance influences reaction kinetics, leading to varied product distributions. Furthermore, 3-AQC's ability to engage in π-stacking interactions contributes to its stability in solid-state forms, impacting its overall behavior in chemical processes.

Zacopride hydrochloride

101303-98-4sc-203723
sc-203723A
10 mg
50 mg
$137.00
$555.00
(0)

Zacopride hydrochloride, an SR-3B compound, exhibits distinctive reactivity as an acid halide, characterized by its propensity to engage in rapid acylation reactions. The compound's unique electronic structure allows for selective interactions with various nucleophiles, leading to a range of reaction kinetics. Its hydrophilic nature, stemming from the presence of charged groups, influences solvation dynamics and can alter its behavior in different solvent systems, enhancing its versatility in synthetic applications.

Mosapride citrate

112885-42-4sc-203635
sc-203635A
10 mg
50 mg
$102.00
$405.00
(0)

Mosapride citrate, classified as an SR-3B compound, showcases remarkable reactivity as an acid halide, primarily through its ability to form stable intermediates during acylation. Its unique steric configuration facilitates specific interactions with nucleophiles, resulting in diverse reaction pathways. Additionally, the compound's polar functional groups enhance solubility and influence its aggregation behavior, which can affect its reactivity in various chemical environments.