OSR2 inhibitors represent a class of chemical compounds specifically designed to target and modulate the activity of oxidative stress-responsive 1 (OSR1) and oxidative stress-responsive kinase 2 (OSR2). These kinases play crucial roles in cellular signaling pathways that regulate ion transport and maintain cellular homeostasis. OSR1 and OSR2 are members of the serine/threonine-protein kinase family and are implicated in various physiological processes, including the control of ion transport across cell membranes. One of the primary functions of OSR2 is its involvement in the regulation of ion channels, such as the WNK (with-no-lysine) family of serine-threonine kinases, which are key regulators of ion transport and blood pressure. OSR2 inhibitors act by interfering with the enzymatic activity of OSR2, thereby modulating downstream signaling pathways involved in ion transport.
The development of OSR2 inhibitors stems from the recognition of the essential roles played by OSR1 and OSR2 in cellular processes, particularly in maintaining ion balance. By selectively inhibiting the catalytic activity of OSR2, these compounds hold promise in unraveling the intricate signaling mechanisms associated with ion transport. The detailed understanding of the structural and biochemical aspects of OSR2 inhibition provides a foundation for the rational design of these compounds, allowing for the exploration of potential applications in various biological contexts.
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