C11orf41_D430041D05Rik Inhibitors constitute a class of compounds that modulate the orphan protein C11orf41, either directly or through linked cellular processes and pathways. Since the function and associated pathways of C11orf41 are not yet well-characterized, inhibitors often target mechanisms commonly affected by orphan proteins. For example, MG-132 is a proteasome inhibitor that can impede protein degradation pathways where C11orf41 may be active. LY294002 and Wortmannin inhibit PI3K and thus affect a range of downstream signaling events that could involve C11orf41. Similarly, 3-Methyladenine and Bafilomycin A1 inhibit autophagy, affecting protein recycling processes in which C11orf41 may participate.
Further, inhibitors like SP600125 and U0126 target JNK and MEK respectively, providing a grip on stress-response and MAPK/ERK signaling pathways. Rapamycin inhibits mTOR, a key regulator of cell growth and protein synthesis, thereby modulating cellular systems where C11orf41 plays a role. Compounds like GW4869 and DAPT target specific enzymes like neutral sphingomyelinase and gamma-secretase, affecting lipid signaling and cellular differentiation pathways respectively. These compounds collectively offer a multifaceted approach to inhibit the biological activities associated with C11orf41, even though the precise roles and pathways of this protein are not yet defined.
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