Chemical inhibitors of 9630058J23Rik function through various mechanisms by interfering with signaling cascades that ultimately control the activity of this protein. Wortmannin and LY294002 are both inhibitors of phosphoinositide 3-kinases (PI3Ks), which play a pivotal role in activating AKT signaling pathways. By inhibiting PI3K, these chemicals lead to a decrease in AKT phosphorylation. Since AKT is a key regulator of numerous substrates including 9630058J23Rik, its inhibition results in reduced activity of 9630058J23Rik. Similarly, Rapamycin acts on the mammalian target of rapamycin (mTOR) pathway, another critical regulator of cell growth and proliferation. By inhibiting mTOR, Rapamycin indirectly decreases the activity of downstream proteins like 9630058J23Rik that are involved in these cellular processes.
Other inhibitors target different kinases within cellular signaling networks. PD98059 and U0126 both target MEK1/2, which are upstream of extracellular signal-regulated kinases (ERK). Inhibition of MEK leads to decreased activation of ERK, which in turn can reduce the phosphorylation level and activity of 9630058J23Rik. SB203580 specifically inhibits p38 MAP kinase, and SP600125 targets JNK, both of which are part of the mitogen-activated protein kinase (MAPK) pathways. These inhibitors reduce the activation of transcription factors and other substrates associated with these pathways, resulting in decreased regulation of proteins like 9630058J23Rik. PP2 inhibits the Src family kinases, leading to a reduction in the activation of several downstream signaling proteins including 9630058J23Rik. Dasatinib, being a broad-spectrum tyrosine kinase inhibitor, affects multiple pathways and kinases, including Src, which in turn affects the activity of 9630058J23Rik. Lastly, chemicals like Bortezomib and MG132 inhibit the proteasome, a complex that degrades ubiquitinated proteins. This inhibition can lead to the accumulation of proteins that regulate the stability and activity of substrates such as 9630058J23Rik, thereby affecting its function. ZM336372 specifically inhibits RAF kinase, thereby attenuating the MAPK pathway and subsequently decreasing the activity of proteins like 9630058J23Rik that lie downstream of this pathway.
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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 | |
| Wortmannin is a potent inhibitor of PI3K, which is crucial for AKT signaling; the inhibition of PI3K leads to reduced AKT activation that can inhibit the phosphorylation status and activity of 9630058J23Rik. | ||||||
| Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
| Rapamycin inhibits mTOR, a central protein in regulating cell growth and proliferation; by inhibiting mTOR, the downstream effect includes the inhibition of proteins involved in cell cycle progression and growth, such as 9630058J23Rik. | ||||||
| PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
| PD98059 selectively inhibits MEK, which is upstream of ERK in the MAPK pathway; inhibiting MEK leads to decreased ERK activity, which can reduce the phosphorylation and activity of proteins like 9630058J23Rik that are substrates for ERK. | ||||||
| LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
| LY294002 is another PI3K inhibitor, leading to decreased AKT phosphorylation; this reduction in AKT activity can inhibit downstream proteins that depend on AKT signaling, including 9630058J23Rik. | ||||||
| SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
| SB203580 is a specific inhibitor of p38 MAPK; by inhibiting p38 MAPK, it can decrease the activation of substrates and transcription factors that are involved in the regulation of proteins like 9630058J23Rik. | ||||||
| SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
| SP600125 is an inhibitor of JNK, part of the MAPK pathway; inhibition of JNK can lead to reduced activity of transcription factors that regulate proteins involved in cell stress responses, including 9630058J23Rik. | ||||||
| U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
| U0126 inhibits MEK1/2, and therefore can reduce ERK phosphorylation and activity; this can lead to reduced function of proteins that are regulated by the ERK pathway, such as 9630058J23Rik. | ||||||
| PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $92.00 $223.00 | 30 | |
| PP2 is an Src family kinase inhibitor; by inhibiting Src kinase activity, it can reduce the phosphorylation and activation of downstream proteins that are regulated by Src, including 9630058J23Rik. | ||||||
| Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
| Dasatinib is a broad-spectrum tyrosine kinase inhibitor that can affect multiple pathways, including Src kinases; by inhibiting these kinases, Dasatinib can reduce the activity of proteins like 9630058J23Rik that are downstream of Src signaling. | ||||||
| Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
| Bortezomib is a proteasome inhibitor; by inhibiting the proteasome, it can lead to the accumulation of ubiquitinated proteins and the potential degradation of regulatory factors involved in the stability and activity of proteins like 9630058J23Rik. | ||||||