LOC100041371 inhibitors like Wortmannin and U0126 represent the class's capacity to impede key signaling cascades, such as those mediated by PI3K and MEK1/2, respectively. These compounds can disrupt the phosphorylation-dependent modulation of proteins, which is a critical mechanism by which cellular responses and activities are regulated. Gö 6983 and Chelerythrine, as inhibitors of protein kinase C, can similarly alter the phosphorylation landscape and thereby influence the activity states of proteins. Compounds like Cyclosporin A and KN-93 exhibit the class's ability to intervene in calcium-dependent signaling events. Cyclosporin A's inhibition of calcineurin affects T-cell activation and other calcium-dependent processes, while KN-93's targeting of Ca2+/calmodulin-dependent protein kinase II can alter calcium signaling pathways that are pivotal for the regulation of numerous proteins.
The inclusion of 5-Azacytidine and Alsterpaullone in this class emphasizes the potential to impact gene expression and cell cycle progression. By affecting DNA methylation and cyclin-dependent kinases, these inhibitors can influence the synthesis and function of proteins. Tunicamycin's role in impeding N-linked glycosylation touches upon the importance of post-translational modifications for protein folding and stability, indicating how changes in these processes can affect protein function. Bortezomib serves as a proteasome inhibitor within the class, highlighting the control over protein degradation. By preventing the breakdown of proteins, bortezomib can lead to an alteration in the levels of proteins within the cell, which can have widespread effects on cellular function.
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