YPEL2 inhibitors like Rapamycin, LY294002, and wortmannin, target the PI3K/AKT/mTOR pathway, which is critical for cellular growth and survival, and their inhibitory action can lead to decreased YPEL2 activity or expression. Similarly, compounds like U0126, SP600125, and SB203580 that inhibit MAPK signaling could alter YPEL2 functions, presuming its involvement in cell cycle control and apoptosis.
Trichostatin A, a histone deacetylase inhibitor, can change gene expression profiles, potentially affecting YPEL2 expression. Conversely, 17-AAG destabilizes proteins by inhibiting the chaperone protein Hsp90, which may include YPEL2 among its client proteins. Roscovitine targets cyclin-dependent kinases and may suppress YPEL2 activity by hindering cell division. Compounds that disrupt organelle function, such as brefeldin A and thapsigargin, can also indirectly impact YPEL2; brefeldin A interrupts protein trafficking, and thapsigargin triggers ER stress, both of which could modify YPEL2's cellular context and activity.Each chemical in the YPEL2 inhibitor class operates on distinct intracellular targets, indirectly influencing the functional landscape in which YPEL2 operates.
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