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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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Inhibits PI3K, which is essential in downstream signaling pathways that 1700021F05Rik may rely on for its function. Inhibition of PI3K can lead to reduced activity of AKT, thereby inhibiting the protein's function related to cell survival and growth signals. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Specifically binds to mTOR (mammalian target of rapamycin), inhibiting the mTORC1 complex which could be crucial for the 1700021F05Rik protein's role in cell growth and proliferation. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
A potent inhibitor of protein kinases. It can inhibit a broad range of kinases that might be necessary for the phosphorylation events that regulate 1700021F05Rik activity. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
A specific inhibitor of PI3K, leading to the inhibition of the Akt pathway which could be integral for 1700021F05Rik's role in regulating cell growth and survival. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
Specifically inhibits MEK1/2, which are upstream regulators of the ERK pathway, potentially reducing the phosphorylation and activity of 1700021F05Rik if it is an ERK pathway-associated protein. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
Inhibits p38 MAP kinase, which may be involved in the signaling pathways that regulate 1700021F05Rik's function, particularly in stress response and cytokine production. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
A selective inhibitor of MEK, which could inhibit the activation of MAPK/ERK pathway, potentially hindering the activity of 1700021F05Rik if it relies on this pathway for its function. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
Inhibits the JNK pathway, which could restrict the functional activity of 1700021F05Rik if it is involved in JNK-mediated cellular processes like apoptosis or inflammation. | ||||||
ZM-447439 | 331771-20-1 | sc-200696 sc-200696A | 1 mg 10 mg | $150.00 $349.00 | 15 | |
A selective inhibitor of Aurora kinases, which may be required for the cell cycle-related functions of 1700021F05Rik, leading to the inhibition of its role in mitosis. | ||||||
Triciribine | 35943-35-2 | sc-200661 sc-200661A | 1 mg 5 mg | $102.00 $138.00 | 14 | |
Specifically inhibits Akt phosphorylation and activation, which might be necessary for the downstream signaling that regulates 1700021F05Rik activity. | ||||||