AVP receptor V3 inhibitors belong to a specialized class of chemical compounds designed to target the AVP (Arginine Vasopressin) receptor V3, also known as the vasopressin 1B receptor (V1B receptor). These receptors are part of the vasopressin receptor family, which includes V1A, V1B (V3), and V2 receptor subtypes. AVP is a peptide hormone that plays essential roles in regulating various physiological processes, including water reabsorption in the kidneys, vasoconstriction, and the stress response. The V3 receptor subtype, which is predominantly found in the anterior pituitary gland and certain brain regions, is primarily associated with the modulation of the hypothalamic-pituitary-adrenal (HPA) axis and the release of adrenocorticotropic hormone (ACTH) in response to stress.
Inhibitors targeting AVP receptor V3 are designed to interact with this receptor and modulate its activity, influencing the downstream signaling pathways and physiological responses associated with AVP-V3 receptor activation. These inhibitors may operate through various mechanisms, such as binding to specific receptor sites or altering receptor conformation. By inhibiting AVP receptor V3, these compounds can affect the stress response, hormone secretion, and other processes regulated by the HPA axis. Research on AVP receptor V3 inhibitors is primarily focused on unraveling the molecular mechanisms underlying the function of this receptor subtype and its role in stress-related physiology and behavior, contributing to our understanding of neuroendocrinology and the intricacies of the stress response system.
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