Date published: 2025-9-13

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FLJ31485 Inhibitors

FLJ31485 inhibitors are not defined by a specific chemical class, instead, they encompass a diverse range of compounds that influence various cellular pathways which could indirectly lead to the inhibition of FLJ31485. For instance, kinase inhibitors such as staurosporine may prevent the phosphorylation state that is required for FLJ31485 activation or function. Similarly, compounds that influence the PI3K/AKT/mTOR pathway, like LY294002 and rapamycin, could potentially lead to decreased FLJ31485 activity by inhibiting the pathway's downstream effects on protein synthesis and cell survival, processes in which FLJ31485 might be implicated.

Additionally, the MAPK pathway, which can be affected by compounds such as U0126, SB203580, and PD98059, plays a critical role in transducing extracellular signals to cellular responses. Inhibition of this pathway could reduce the activity of FLJ31485 if it is a downstream effector. Furthermore, cellular energy metabolism and homeostasis are vital for protein function. Inhibitors like 2-Deoxy-D-glucose and WZB117 could lead to decreased FLJ31485 activity by limiting the energy supply or necessary substrates. Thapsigargin's role in disrupting calcium homeostasis may also inhibit FLJ31485 activity if it is regulated by calcium signaling.

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