Date published: 2025-12-5

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bradykinin B2 R Inhibitors

The chemical class known as "bradykinin B2 receptor inhibitors" encompasses a diverse range of compounds that primarily act as antagonists to the bradykinin B2 receptor (B2R). These inhibitors play a pivotal role in regulating the physiological functions mediated by B2R, with a particular emphasis on its involvement in inflammatory responses and vasodilation. It's important to note that the mechanisms underlying the inhibition of B2R activation can vary significantly among these compounds. Some of these inhibitors, such as LY303870, LF 22-0542, and FR 173657, fall into the category of non-peptide antagonists. Despite their structural dissimilarity to bradykinin, they effectively block B2R activation. This intriguing feature sets them apart from their peptide counterparts and introduces a distinct pharmacological profile. This diversity within the class of B2R inhibitors not only underscores the complexity of receptor modulation but also provides researchers and clinicians with a broader range of tools to target B2R in different pathological conditions where its dysregulation plays a critical role. In conclusion, the chemical class of "bradykinin B2 receptor inhibitors" encompasses both peptide and non-peptide compounds that act as antagonists to B2R. These inhibitors serve as indispensable tools for fine-tuning the receptor's role in various physiological processes, particularly in the context of inflammatory responses and vasodilation. Their specificity and structural diversity highlight their ability in precisely modulating B2R activity, offering promise for targeted interventions in numerous medical conditions characterized by B2R dysfunction.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

WIN 64338 hydrochloride

163727-74-0sc-204398
sc-204398A
1 mg
5 mg
$209.00
$852.00
1
(0)

WIN 64338 hydrochloride acts as a potent antagonist of bradykinin B2 receptors, exhibiting unique binding characteristics that disrupt typical receptor-ligand interactions. Its molecular structure promotes specific conformational changes upon binding, influencing downstream signaling pathways. The hydrochloride form enhances solubility, allowing for efficient distribution in biological systems. Furthermore, its kinetic profile suggests a rapid onset of action, impacting cellular signaling dynamics significantly.