C11orf74 inhibitors, given the protein's known role in autophagy, largely pivot around modulating this intricate cellular process. Notably, a vast array of these inhibitors act upon the phosphatidylinositol 3-kinase (PI3K) pathways. Molecules such as 3-Methyladenine, Wortmannin, and LY294002 directly impede PI3K or its variants,steering C11orf74's functional activity within autophagy. On the other hand, Bafilomycin A1 and Chloroquine target the fusion of autophagosomes with lysosomes, a later stage in the autophagic process, thus indirectly delineating the overall functional context in which C11orf74 operates.
Moreover, considering mTOR's central regulatory role in autophagy, inhibitors like Torin1 and Rapamycin, or like MHY1485, bring forth a broader modulation of the autophagy landscape, which can in turn influence C11orf74's function. By adjusting the balance of autophagic flux through these chemical entities, one may achieve an indirect modulation of C11orf74 activity, making these compounds valuable tools for research into the protein's function and involvement in cellular processes.
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