ASB-12 Activators are chemical compounds that have the potential to indirectly enhance the functional activity of ASB-12, a protein that is likely involved in the ubiquitin-proteasome system, governing protein turnover and degradation. Compounds such as Triterpenoid saponin and Artemisinin can activate cellular stress and autophagy pathways, respectively, that are closely associated with protein degradation systems. The activation of these pathways can lead to a higher demand for proteasomal activity, which might indirectly activate ASB-12 as it may be implicated in tagging proteins for degradation. Forskolin's elevation of cAMP levels can activate PKA, leading to phosphorylation events that could include substrates of ASB-12 or regulatory proteins that control its activity. Piceatannol's inhibition of Syk kinase may relieve inhibition on ubiquitin ligases such as ASB-12, enhancing its functional role in the cell.
Furthermore, compounds like Curcumin, Withaferin A, and Sulforaphane modulate the NF-κB and Nrf2 pathways, which have downstream effects on the expression and activity of components in the ubiquitin-proteasome system, potentially affecting ASB-12's role in this process. Resveratrol's activation of SIRT1 could lead to the deacetylation of proteins that are substrates for ubiquitination, which would enhance the requirement for ASB-12's ligase activity. EGCG's inhibition of histone deacetylases and Oltipraz's activation of Nrf2 could lead to changes in gene expression patterns that increase the need for ASB-12-mediated protein turnover. Piperlongumine's alteration of ROS levels can influence various signaling pathways, some of which may involve ASB-12's ubiquitination targets.
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