Chemical inhibitors of FILIP1L can impact various cellular pathways and processes by targeting specific enzymes and kinases that play a role in the regulation of this protein's function. For instance, Palbociclib, a selective inhibitor of cyclin-dependent kinases CDK4 and CDK6, can lead to reduced cell proliferation by indirectly inhibiting FILIP1L functions associated with cell cycle progression. Similarly, Rapamycin, which inhibits the mTOR pathway, can suppress the pathways involving FILIP1L in cell growth and survival. Trichostatin A, an inhibitor of histone deacetylase, can alter the chromatin structure, potentially affecting the pathways necessary for FILIP1L's role in gene expression regulation.
Furthermore, LY294002 and Wortmannin are both PI3K inhibitors that can reduce Akt signaling, thereby inhibiting FILIP1L-associated functions in cell survival and growth. U0126 and PD98059, both inhibitors of MEK1/2, impact the ERK pathway, which is involved in processes that FILIP1L influences, such as cell differentiation and proliferation. SB203580, which inhibits p38 MAP kinase, can lead to the functional inhibition of FILIP1L's roles in response to cellular stress. In addition to these, Y-27632, a ROCK inhibitor, can lead to cytoskeletal changes that inhibit FILIP1L's functions related to cell movement and structure. SP600125, an inhibitor of JNK, can inhibit FILIP1L's role in apoptosis signaling pathways. Lastly, imatinib and sunitinib target tyrosine kinases and receptor tyrosine kinases, respectively, which are involved in signaling pathways that can affect FILIP1L's role in processes such as actin filament dynamics and cell growth.
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