Chemical inhibitors of 1500005A01Rik can be categorized based on the signaling pathways they target to exert their inhibitory effects. Wortmannin and LY294002 are both inhibitors of PI3K, an upstream regulator of the Akt/mTOR signaling pathway. By inhibiting PI3K, these chemicals prevent the propagation of signals that are essential for the function of 1500005A01Rik. In a similar vein, Triciribine directly targets Akt, impeding its ability to phosphorylate downstream targets that are involved in the functional activity of 1500005A01Rik. Rapamycin, another inhibitor, exerts its effects by specifically binding to mTOR, a central protein in the PI3K/Akt/mTOR pathway, which is crucial for cell growth and proliferation signals that may be necessary for the activity of 1500005A01Rik.
Furthermore, PD98059 and U0126 act upon the MAPK/ERK pathway by selectively inhibiting MEK. This inhibition results in the suppression of ERK-mediated signaling, which can have downstream effects on the activity of 1500005A01Rik. SB203580 and SP600125, inhibit p38 MAPK and JNK respectively, both of which are part of the MAPK pathway. By impeding these kinases, SB203580 and SP600125 disrupt the signaling events that regulate the functional state of 1500005A01Rik. The EGFR tyrosine kinase inhibitors, Gefitinib and Erlotinib, obstruct the kinase activity of EGFR which participates in multiple signaling pathways, including those that may engage 1500005A01Rik. Lapatinib extends this concept by targeting both EGFR and HER2/neu receptors, which are implicated in the PI3K/Akt/mTOR pathway that can be linked to the function of 1500005A01Rik. Lastly, Sorafenib, by inhibiting multiple tyrosine protein kinases, can impede the downstream signaling pathways critical for the function of 1500005A01Rik, thereby leading to its functional inhibition.
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