The class of BVES Inhibitors comprises a range of chemical compounds that indirectly inhibit the activity or influence of the Blood Vessel Epicardial Substance protein through various signaling pathways and cellular processes. These inhibitors target different aspects of cellular signaling and function, which are interconnected with the roles and effects of BVES in cells. For instance, inhibitors of the Wnt and Hedgehog pathways impact cellular differentiation and migration, processes where BVES has a significant role. Similarly, compounds like GSK-3β, PI3K, and Akt inhibitors affect downstream effects of these pathways, thereby indirectly modulating the activity related to BVES.
These inhibitors are not specific to BVES but influence the protein's function by altering related signaling cascades and cellular mechanisms. This includes modulation of kinase activities, transcription factors, and other signaling molecules like ROCK, MAPK, JNK, and NF-κB. By affecting these pathways, the inhibitors contribute to changes in cellular processes like proliferation, apoptosis, stress responses, and cytoskeletal dynamics, all of which are crucial to the functional context of BVES. Additionally, agents like calcium channel blockers and histone deacetylase inhibitors demonstrate the broad spectrum of mechanisms through which these compounds can indirectly influence BVES activity, emphasizing the complex network of cellular signaling in which BVES is embedded.
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