Date published: 2025-9-17

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V1RC26 Inhibitors

V1RC26 inhibitors are chemical compounds designed to specifically target and inhibit the function of the V1RC26 protein, a member of the vasopressin receptor family involved in signal transduction pathways. V1RC26 is typically associated with the regulation of water balance, vascular tone, and smooth muscle contraction through its interactions with vasopressin, a peptide hormone. These inhibitors work by binding to critical regions of the V1RC26 receptor, preventing vasopressin from activating the receptor and disrupting its downstream signaling cascade. This interference affects the receptor's ability to mediate its usual physiological functions, leading to altered cellular responses to external stimuli.

Structurally, V1RC26 inhibitors are often designed to interact with the receptor's binding pocket or allosteric sites, which are essential for ligand binding and activation. By blocking these sites, the inhibitors prevent the receptor from undergoing the conformational changes required for signal transduction. Some inhibitors may act by stabilizing the inactive form of V1RC26, while others might prevent the receptor from interacting with G-proteins, which are critical mediators in its signaling pathway. The inhibition of V1RC26 provides researchers with tools to investigate the role of this receptor in various biological processes such as fluid homeostasis, vascular function, and cellular signaling. These compounds enable the detailed study of receptor-ligand interactions, signal modulation, and the broader impact of V1RC26 on cellular physiology. Through such research, scientists can gain a better understanding of how specific signaling pathways contribute to the regulation of complex physiological systems.

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