Date published: 2026-5-18

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BRS-3 Inhibitors

BRS-3 inhibitors constitute a class of chemical compounds specifically designed to target and modulate the activity of the Bombesin receptor subtype 3 (BRS-3), a G-protein-coupled receptor (GPCR) that belongs to the bombesin receptor family. These inhibitors play a crucial role in advancing our understanding of the physiological and pathophysiological processes associated with the BRS-3 receptor. The primary objective of BRS-3 inhibitors is to manipulate the receptor's activity, either by blocking its function or modulating its signaling pathways. By doing so, these inhibitors enable researchers to elucidate the receptor's role in various cellular and physiological processes, shedding light on its involvement in different aspects of biology. Chemically, BRS-3 inhibitors can encompass a diverse range of small molecules, peptides, or compounds with structures tailored to interact with BRS-3. Mechanistically, these inhibitors function through multiple pathways. Some act as competitive antagonists, binding to the receptor's active site, thereby blocking receptor activation. Others may influence BRS-3 by altering its conformation or cellular trafficking, effectively modulating its surface expression and downstream signaling. Furthermore, some BRS-3 inhibitors may target the intracellular cascades activated by the receptor, disrupting the receptor's signaling networks and attenuating its function. These inhibitors provide invaluable tools for researchers to probe BRS-3's role in cellular physiology, which can have implications for understanding fundamental biological processes and may ultimately contribute to the development of novel pharmacological interventions in the future.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

SR 144528

192703-06-3sc-224292
sc-224292A
5 mg
10 mg
$282.00
$539.00
6
(1)

SR-144528 is a selective antagonist of BRS3, binding to its receptor and blocking its activation. This inhibition prevents the downstream signaling cascade, effectively reducing the receptor's activity.