Date published: 2025-12-15

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11beta-HSD1 Inhibitors

Santa Cruz Biotechnology now offers a broad range of 11beta-HSD1 Inhibitors for use in various applications. 11beta-HSD1 inhibitors are specialized compounds designed to inhibit the enzyme 11β-hydroxysteroid dehydrogenase type 1, which is crucial for the conversion of inactive cortisone to active cortisol in tissues. This enzyme plays a significant role in regulating local glucocorticoid levels, impacting various physiological processes such as metabolism, immune response, and stress adaptation. In scientific research, 11beta-HSD1 inhibitors are invaluable for studying the role of glucocorticoid metabolism in metabolic disorders, obesity, and insulin resistance. These inhibitors help researchers explore the enzyme's contribution to the pathogenesis of these conditions by modulating cortisol levels at the tissue level. By inhibiting 11beta-HSD1, scientists can dissect the effects of altered glucocorticoid activity on cellular functions, including lipid metabolism, glucose homeostasis, and inflammatory responses. The high purity and specificity of 11beta-HSD1 inhibitors provided by Santa Cruz Biotechnology ensure reliable and reproducible results, facilitating advanced research in endocrinology and metabolic disease. By offering a comprehensive selection of these inhibitors, Santa Cruz Biotechnology supports the scientific community in developing new experimental models and uncovering novel insights into the regulation of glucocorticoid action. View detailed information on our available 11beta-HSD1 Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

4,4-Difluorocyclohexanamine Hydrochloride

675112-70-6sc-206942
250 mg
$400.00
(0)

4,4-Difluorocyclohexanamine Hydrochloride exhibits distinctive interactions with 11beta-HSD1, characterized by its ability to form strong ionic bonds and engage in steric hindrance. This compound influences the enzyme's active site dynamics, enhancing substrate affinity and altering reaction rates. Its unique fluorinated structure contributes to increased lipophilicity, facilitating selective binding and modulation of metabolic pathways, ultimately affecting glucocorticoid regulation.