AMPKβ1 inhibitors are a class of chemical compounds that specifically target the β1 subunit of AMP-activated protein kinase (AMPK), a crucial energy-sensing enzyme that regulates cellular energy homeostasis. AMPK is a heterotrimeric complex consisting of α (catalytic), β (scaffolding), and γ (regulatory) subunits. The β1 subunit serves as a scaffolding component, helping to bridge the α and γ subunits, while also containing a glycogen-binding domain that allows AMPK to sense cellular energy status in response to metabolic stress. By inhibiting the β1 subunit, these compounds disrupt the assembly and proper functioning of the AMPK complex, affecting its ability to regulate energy balance in cells.
The mechanism of action for AMPKβ1 inhibitors typically involves direct binding to the β1 subunit, either preventing its interaction with the other subunits or inhibiting its role in energy sensing and glycogen binding. This disruption hinders AMPK's ability to activate downstream pathways that modulate cellular processes such as glucose uptake, lipid metabolism, and mitochondrial biogenesis. AMPKβ1 inhibitors are important tools for studying the specific role of the β1 subunit in AMPK activity and the broader regulatory mechanisms involved in cellular metabolism. By inhibiting this subunit, researchers can explore how AMPK functions are altered in response to changes in energy status and how different subunit configurations influence the overall metabolic control within cells. These inhibitors provide valuable insights into the complexities of AMPK signaling, helping to dissect the distinct contributions of each subunit to cellular energy regulation.
SEE ALSO...
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
BML-275 | 866405-64-3 | sc-200689 sc-200689A | 5 mg 25 mg | $94.00 $348.00 | 69 | |
A selective AMPK inhibitor that binds to the β1 subunit, impairing the assembly of the AMPK complex. | ||||||
SBI-0206965 | 1884220-36-3 | sc-507431 | 10 mg | $122.00 | ||
A selective inhibitor that targets AMPK, reducing its activity by interfering with the AMP binding. | ||||||
STO-609 | 52029-86-4 | sc-507444 | 5 mg | $140.00 | ||
Inhibits the upstream kinase CaMKKβ, thereby reducing AMPK activation indirectly. |