Date published: 2026-1-10

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AVP Receptor V Inhibitors

Santa Cruz Biotechnology now offers a broad range of AVP Receptor V Inhibitors for use in various applications. AVP (arginine vasopressin) receptor V inhibitors target the V receptors of vasopressin, a key hormone involved in regulating water balance, blood pressure, and various other physiological processes. These receptors are part of a G-protein-coupled receptor family that includes V1, V2, and V3 subtypes, each with distinct roles in cellular signaling. By inhibiting these receptors, particularly the V2 receptor, researchers can explore the pathways by which vasopressin exerts its effects on the body, such as promoting water reabsorption in the kidneys, modulating vascular tone, and influencing the release of various hormones. AVP receptor V inhibitors are critical tools in scientific research aimed at understanding the complex signaling networks that govern fluid homeostasis and vascular function. These inhibitors are employed in studies focused on dissecting the molecular mechanisms of vasopressin signaling and its interactions with other hormonal pathways, providing insights into how disruptions in these processes may contribute to conditions like hypertension, heart failure, and kidney dysfunction. Additionally, AVP receptor V inhibitors are used in research exploring the receptor's role in stress responses and social behavior, where vasopressin is known to have significant effects. The availability of a diverse range of AVP receptor V inhibitors allows scientists to design experiments tailored to specific aspects of vasopressin receptor function, advancing our understanding of this crucial hormone's role in both normal physiology and disease. View detailed information on our available AVP Receptor V Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

OPC 21268

131631-89-5sc-362775
sc-362775A
5 mg
25 mg
$137.00
$681.00
(0)

OPC 21268 functions as a selective antagonist for AVP receptor V, exhibiting unique binding affinity that alters receptor conformation and downstream signaling cascades. Its molecular interactions are characterized by specific hydrogen bonding and hydrophobic contacts, which modulate G-protein coupling efficiency. This compound influences intracellular signaling pathways, impacting cellular responses and contributing to the dynamic regulation of osmotic balance and fluid homeostasis.