Date published: 2025-12-3

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SR-2C Activators

SR-2C activators represent a specific chemical class characterized by their ability to modulate the activity of the serotonin receptor subtype 2C, abbreviated as 5-HT2C. These receptors belong to the broader family of serotonin receptors, which are proteins found in the central nervous system and peripheral tissues, playing a pivotal role in regulating various physiological and neurological functions. The SR-2C activators interact with the 5-HT2C receptor, which is a G-protein coupled receptor (GPCR), and they do so in a manner that can either enhance or inhibit its signaling pathways. This modulation of receptor activity is essential for understanding the intricate neurochemical processes that influence mood, behavior, and other physiological responses. Chemically, SR-2C activators encompass a diverse array of compounds, including small organic molecules, peptides, and even natural products. Their interaction with the 5-HT2C receptor may result in either an agonistic or antagonistic effect, leading to changes in downstream signaling pathways. Such modulation can have profound implications for various physiological functions, as the 5-HT2C receptor is involved in the regulation of appetite, mood, and sleep, among other processes. The intricate mechanisms underlying the interaction between SR-2C activators and the 5-HT2C receptor continue to be a subject of intensive research, shedding light on the complex neurobiology of serotonin receptors.

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Items 21 to 26 of 26 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

1-(6-Benzofuranyl)-2-propanone

286836-34-8sc-391569
100 mg
$360.00
(0)

1-(6-Benzofuranyl)-2-propanone, an SR-2C compound, showcases intriguing reactivity patterns attributed to its aromatic structure, which enhances electron delocalization. This feature allows for selective electrophilic substitution reactions, particularly with nucleophiles. The compound's unique steric hindrance influences its interaction dynamics, leading to distinct reaction pathways. Additionally, its ability to form stable intermediates can significantly alter kinetic profiles, making it a fascinating subject for synthetic exploration.

1-(3-Chlorophenyl)piperazine monohydrochloride

13078-15-4sc-264551
10 g
$123.00
(0)

1-(3-Chlorophenyl)piperazine monohydrochloride, classified as an SR-2C compound, exhibits notable characteristics due to its piperazine ring and chlorophenyl substituent. The presence of the chlorine atom introduces unique electronic effects, enhancing its reactivity towards nucleophiles. This compound can engage in hydrogen bonding, influencing solubility and stability in various environments. Its distinct conformational flexibility allows for diverse interaction mechanisms, making it a compelling candidate for further study in synthetic chemistry.

RS 102221 hydrochloride

185376-97-0sc-491403
sc-491403A
5 mg
25 mg
$190.00
$446.00
(0)

RS 102221 hydrochloride, an SR-2C compound, features a unique structural framework that facilitates specific molecular interactions. Its distinct electronic configuration promotes selective reactivity with electrophiles, while the presence of halogen atoms enhances its dipole moments, influencing solvation dynamics. The compound's ability to adopt multiple conformations allows for varied reaction pathways, making it an intriguing subject for exploration in chemical synthesis and reactivity studies.

Valproic Acid

99-66-1sc-213144
10 g
$85.00
9
(1)

Valproic acid is an anticonvulsant and mood stabilizer that may influence serotonin receptor expression and function, including the 5-HT2C receptor.

Risperidone

106266-06-2sc-204881
sc-204881A
sc-204881B
sc-204881C
10 mg
50 mg
1 g
5 g
$171.00
$705.00
$1000.00
$2000.00
1
(1)

Risperidone is an atypical antipsychotic with a high affinity for 5-HT2A and 5-HT2C receptors, and it is thought to modulate serotonin neurotransmission.

1-(3-Chlorophenyl)piperazine

6640-24-0sc-206098
5 mg
$330.00
(1)

1-(3-Chlorophenyl)piperazine, classified as an SR-2C compound, exhibits intriguing steric and electronic properties that influence its reactivity. The chlorophenyl group introduces significant electron-withdrawing effects, enhancing nucleophilicity in certain contexts. Its piperazine ring allows for diverse conformational flexibility, which can lead to varied interaction profiles with substrates. This compound's unique spatial arrangement and polar characteristics make it a fascinating candidate for studying reaction mechanisms and molecular dynamics.