LOC729465 Inhibitors such as Wortmannin and LY294002 target the PI3K/Akt pathway, a critical signaling cascade in cell survival and metabolism, which could affect LOC729465 if it is a component or regulator within this pathway. Similarly, compounds like U0126 and PD98059 act on the MAPK/ERK pathway, which is crucial for cell proliferation and differentiation. Their inhibitory action on MEK1/2 could lead to downstream effects on LOC729465 if it is involved in this pathway. Compounds like SB203580 and SP600125 target the stress-activated MAP kinases p38 and JNK, respectively, offering another potential route to modulate LOC729465 activity by altering the response to cellular stress or inflammatory signals.
The mTOR pathway, implicated in cell growth and autophagy, can be modulated by rapamycin, which could impact LOC729465 if it plays a role in these processes. Furthermore, PP2 focuses on Src family tyrosine kinases, which are important for multiple signaling pathways, including those related to cell adhesion, migration, and proliferation. By inhibiting these kinases, PP2 may affect LOC729465 activity. Bortezomib disrupts the ubiquitin-proteasome pathway, which is essential for protein turnover and could potentially lead to altered levels of LOC729465 or its regulatory proteins. Thapsigargin, by inhibiting SERCA, could disrupt intracellular calcium levels, influencing signaling pathways where calcium acts as a secondary messenger; this could extend to pathways involving LOC729465. Lastly, ZM-447439, targeting Aurora kinases involved in cell cycle progression, could indirectly affect LOC729465 if it is linked to cell cycle control.
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