Ssn6 inhibitors are primarily centered on influencing the activity of the Tup1-Ssn6 co-repressor complex in yeast. As a critical component of this complex, Ssn6 plays a role in the regulation of various genes. Direct inhibition of Ssn6 is not well-documented, leading us to focus on compounds that modulate related pathways or processes. Notably, histone deacetylase inhibitors like Trichostatin A and Sodium butyrate can modify the chromatin structure, impacting the binding and activity of the Tup1-Ssn6 complex.
Furthermore, the DNA methyltransferase inhibitor, 5-Azacytidine, can influence gene expression, providing an indirect avenue to modulate Ssn6 functions. Yeast metabolism and signaling are intricate and interconnected. Compounds such as Miconazole and Fluconazole, which affect ergosterol synthesis, may indirectly affect processes regulated by Tup1-Ssn6. Proteasome and autophagy inhibitors, like MG-132 and 3-Methyladenine respectively, can alter cellular homeostasis and protein interactions, thereby offering influence over the Tup1-Ssn6 complex.
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