Date published: 2025-9-14

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1700021F05Rik Inhibitors

Chemical inhibitors of 1700021F05Rik can exert their inhibitory effects through interference with various signaling pathways that are crucial for the protein's activity. For instance, Wortmannin and LY294002 are phosphoinositide 3-kinases (PI3K) inhibitors. The inhibition of PI3K by these chemicals can lead to a decrease in Akt phosphorylation, which is a key event in signaling pathways associated with cell survival and proliferation, activities in which 1700021F05Rik may play a role. Similarly, Triciribine directly targets Akt, preventing its activation and subsequent downstream signaling that could be vital for 1700021F05Rik's function. By disrupting these pathways, the chemicals ensure that the activation and the regulatory functions of 1700021F05Rik are hindered. Rapamycin binds to mTOR, inhibiting the mTORC1 complex, which is another pathway that could be essential for the cellular processes governed by 1700021F05Rik, such as cell growth and proliferation.

Further, chemicals like U0126 and PD98059 selectively inhibit MEK1/2, which are upstream of ERK. By blocking MEK, these inhibitors would prevent the activation of the ERK pathway, potentially reducing the activity of 1700021F05Rik if it is linked to this pathway. Similarly, SB203580 targets p38 MAP kinase, and SP600125 inhibits the JNK pathway, both of which are important in cellular stress responses and could be relevant to the regulatory functions of 1700021F05Rik. Inhibition of these kinases can suppress the phosphorylation events needed for 1700021F05Rik's activity in these responses. Dasatinib and Sunitinib both act on multiple tyrosine kinases, with Dasatinib inhibiting Src family kinases and c-KIT, and Sunitinib targeting receptor tyrosine kinases, which are often implicated in multiple signaling pathways, including those that 1700021F05Rik may participate in. The inhibition of these kinases can lead to a blockade of the signal transduction necessary for 1700021F05Rik's involvement in cellular processes. Lastly, ZM-447439 targets Aurora kinases, which are critical for cell cycle progression, and its inhibition could impact 1700021F05Rik's function related to mitosis and cell division. Each chemical, by targeting specific proteins or pathways, ensures the functional inhibition of 1700021F05Rik by disrupting the precise cellular mechanisms it relies upon for its activity.

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