Date published: 2025-10-22

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CaMKK beta Inhibitors

Santa Cruz Biotechnology now offers a broad range of CaMKK beta Inhibitors for use in various applications. CaMKK beta inhibitors are essential tools in the study of calcium/calmodulin-dependent protein kinase kinase beta (CaMKKβ), a pivotal enzyme in the regulation of multiple signaling pathways that control cellular processes such as metabolism, cell growth, and neuronal function. CaMKKβ acts as an upstream activator of key kinases like AMP-activated protein kinase (AMPK) and CaMKI/IV, which are involved in energy balance, stress responses, and synaptic plasticity. By using CaMKK beta inhibitors, researchers can specifically block the activation of these downstream targets, allowing for a detailed investigation into how CaMKKβ influences cellular responses to various stimuli, including changes in calcium levels. These inhibitors are widely utilized in research focused on dissecting the role of CaMKKβ in metabolic regulation, particularly in the context of its influence on AMPK, a critical energy sensor in cells. Additionally, CaMKK beta inhibitors are valuable for studying the molecular mechanisms underlying CaMKKβ's involvement in neuronal signaling pathways, where it plays a crucial role in learning, memory, and neuroprotection. By inhibiting CaMKKβ, scientists can gain insights into the complex network of interactions that govern cellular functions and how disruptions in these pathways might contribute to various biological outcomes. The use of CaMKK beta inhibitors spans a variety of experimental models, from cellular assays to in vivo studies, providing essential data that advance our understanding of CaMKKβ's role in health and disease. View detailed information on our available CaMKK beta Inhibitors by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

STO-609 acetate salt

1173022-21-3sc-202820
5 mg
$101.00
19
(2)

STO-609 acetate salt acts as a selective inhibitor of CaMKK beta, engaging with the enzyme's active site to impede its kinase activity. This interaction alters the phosphorylation dynamics of various substrates, impacting metabolic pathways and cellular signaling. Its distinct binding affinity and kinetic properties facilitate nuanced studies of CaMKK beta's role in cellular regulation, while its favorable solubility characteristics support diverse experimental applications.