Chemical inhibitors of 1500035H01Rik can intervene in various signaling pathways to modulate the activity of this protein. Wortmannin and LY294002 are examples that target the PI3K/AKT pathway, which is upstream of 1500035H01Rik. By inhibiting PI3K, these chemicals can reduce the phosphorylation and activation of AKT, subsequently leading to the inhibition of 1500035H01Rik. Another inhibitor, MK-2206, acts more directly by inhibiting AKT itself, hence disrupting the signaling cascade that would normally result in the activation of 1500035H01Rik. Triciribine also follows this route, preventing the phosphorylation and activation of AKT, therefore diminishing the functional activity of 1500035H01Rik.
Moving to other pathways, Rapamycin targets the mTOR pathway, specifically mTORC1, which interacts with signals that affect 1500035H01Rik activity. The inhibition of mTORC1 by Rapamycin can result in decreased activity of proteins in this pathway, including 1500035H01Rik. In the MAPK pathway, U0126, PD98059, and SL327 inhibit MEK1/2, which are upstream of ERK1/2, leading to a reduction in ERK activity. With ERK activity downregulated, the regulatory influence on 1500035H01Rik is reduced, resulting in its functional inhibition. Similarly, SP600125 and SB203580 block the JNK and p38 MAPK pathways, respectively, both of which can have downstream effects on the activity of 1500035H01Rik. Lastly, PP2 and Dasatinib inhibit Src family kinases, affecting multiple signaling pathways that intersect with the functional regulation of 1500035H01Rik. By inhibiting these kinases, these chemicals can suppress the activity of 1500035H01Rik through multiple, possibly intersecting, signaling routes.
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