Date published: 2026-4-26

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Cholecystokinin Receptor Inhibitors

Santa Cruz Biotechnology now offers a broad range of Cholecystokinin Receptor Inhibitors for use in various applications. Cholecystokinin (CCK) receptors are critical components in the regulation of digestive processes, including the release of digestive enzymes and bile, as well as in signaling pathways related to satiety and anxiety. Cholecystokinin Receptor Inhibitors are essential tools in scientific research for exploring the role of CCK receptors in these diverse biological functions. By blocking the activity of these receptors, researchers can investigate the specific mechanisms by which CCK influences physiological responses, providing insights into how these receptors contribute to the regulation of appetite, digestion, and neural signaling. These inhibitors are commonly used in studies aimed at understanding the complex interactions between CCK receptors and their ligands, such as how these interactions affect cellular signaling pathways and physiological outcomes. The use of these inhibitors has significantly advanced research in fields such as neurobiology, gastroenterology, and endocrinology, offering valuable tools for dissecting the intricate signaling networks involving CCK receptors. By providing a means to selectively inhibit these receptors, researchers can gain a deeper understanding of their function and the broader implications of CCK signaling in health and disease. View detailed information on our available Cholecystokinin Receptor Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Lorglumide Sodium

1021868-76-7sc-205734
sc-205734A
25 mg
100 mg
$165.00
$650.00
1
(0)

Lorglumide Sodium functions as a cholecystokinin receptor antagonist, characterized by its ability to disrupt peptide signaling pathways. Its unique molecular architecture enables selective binding to receptor sites, modulating downstream effects on digestive processes. The compound's interactions with lipid membranes influence its bioavailability, while its conformational flexibility allows for dynamic engagement with target proteins, impacting reaction kinetics and cellular responses.