Date published: 2025-9-16

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FLJ36848 Inhibitors

Compounds such as Wortmannin and LY294002 are PI3K inhibitors that can disrupt the PI3K/Akt signaling pathway, a critical cascade in regulating cell survival, growth, and apoptosis. By inhibiting this pathway, these compounds can alter the cellular context in which FLJ36848 may operate. MEK inhibitors like U0126, PD98059, and Selumetinib are capable of blocking the ERK/MAPK pathway, which is involved in cell proliferation and differentiation, potentially intersecting with the biological role of FLJ36848.

SB431542, as a selective inhibitor of TGF-β receptors, can modulate TGF-β signaling, which is crucial for cell growth, differentiation, and immune regulation. DAPT, by inhibiting γ-secretase, can influence the Notch signaling pathway, affecting cell fate decisions that FLJ36848 may be involved in. The proteasome inhibitors MG132 and Bortezomib can prevent the degradation of proteins, potentially leading to an accumulation of regulatory proteins within pathways active in FLJ36848's function. SP600125 is a JNK inhibitor that can affect transcription factor activity and apoptosis, processes that may involve FLJ36848. IKK 16 can disrupt the NF-κB pathway, which regulates inflammation and cell survival, potentially affecting FLJ36848's role in these processes. Rapamycin, an mTOR inhibitor, can impede cell growth and proliferation, affecting the cellular environment of FLJ36848.

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