Chemical inhibitors of 1810022C23Rik can interfere with the protein's function through various molecular pathways. Wortmannin and LY294002 are phosphoinositide 3-kinase (PI3K) inhibitors that can prevent the phosphorylation and activation of Akt, a kinase downstream of PI3K. This can lead to the inhibition of 1810022C23Rik if its functionality is Akt-dependent. Similarly, PD98059 and U0126 can inhibit mitogen-activated protein kinase kinase (MEK1/2), which is upstream of extracellular signal-regulated kinases (ERK1/2). By impeding the MEK-ERK pathway, these compounds can inhibit the function of 1810022C23Rik if it is regulated by this route. SB203580, by selectively inhibiting p38 MAP kinase, can disrupt stress response pathways that may impinge on the functionality of 1810022C23Rik. SP600125, as a c-Jun N-terminal kinase (JNK) inhibitor, can inhibit signaling pathways that control proteins functionally related to 1810022C23Rik, leading to its inhibition.
Furthermore, Dasatinib, a Src family kinase inhibitor, and Imatinib, a tyrosine kinase inhibitor, can also inhibit the function of 1810022C23Rik by targeting kinases that regulate its activity. By inhibiting Src kinases, Dasatinib can suppress the functional activity of 1810022C23Rik. Imatinib, which targets Bcr-Abl, c-Kit, and PDGFR, can accomplish similar inhibition if 1810022C23Rik is regulated by these kinases. Rapamycin inhibits the mammalian target of rapamycin (mTOR), potentially leading to the inhibition of 1810022C23Rik if it is downstream of mTOR signaling. Lastly, multikinase inhibitors such as Sorafenib and Sunitinib can inhibit the function of 1810022C23Rik by targeting various kinases involved in cell signaling mechanisms that regulate proteins like 1810022C23Rik. Sorafenib acts on Raf kinases, VEGFR, and PDGFR, while Sunitinib targets VEGFR, PDGFR, and additional tyrosine kinases. Each of these inhibitors can impede the signaling required for 1810022C23Rik's functionality, thereby inhibiting the protein's 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 | $67.00 $223.00 $425.00 | 97 | |
Wortmannin inhibits phosphoinositide 3-kinases (PI3K), which are involved in various signaling pathways, including those that regulate protein functions similar to 1810022C23Rik. Inhibition of PI3K leads to a decrease in Akt signaling, which can suppress the activation of downstream proteins that are functionally similar to 1810022C23Rik. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
LY294002 is another PI3K inhibitor that prevents the phosphorylation of Akt. By doing this, it disrupts the PI3K/Akt pathway, which is necessary for the full functionality of proteins like 1810022C23Rik. This results in the functional inhibition of the protein's activity. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
PD98059 is a selective inhibitor of mitogen-activated protein kinase kinase (MEK), which acts upstream of extracellular signal-regulated kinases (ERK1/2). By inhibiting MEK, PD98059 indirectly prevents the activation of the ERK pathway, which could reduce the activity of proteins such as 1810022C23Rik that are regulated by this pathway. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $64.00 $246.00 | 136 | |
U0126 functions similarly to PD98059 by selectively inhibiting MEK1 and MEK2, which are essential for the activation of the ERK pathway. The suppression of this pathway can lead to the functional inhibition of proteins, including 1810022C23Rik, that rely on ERK signaling for their activity. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
SB203580 is a selective inhibitor of p38 MAP kinase, which is involved in stress response and cytokine production. By targeting p38 MAP kinase, SB203580 can inhibit signaling pathways that contribute to the functional activity of proteins like 1810022C23Rik, thereby inhibiting the protein's function. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
SP600125 is an inhibitor of c-Jun N-terminal kinase (JNK), which influences various cellular processes including apoptosis and proliferation. Inhibition of JNK can disrupt signaling pathways that may be involved in controlling proteins similar to 1810022C23Rik, resulting in their functional inhibition. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $70.00 $145.00 | 51 | |
Dasatinib is a Src family kinase inhibitor. Src kinases are involved in multiple signaling pathways that regulate various cellular functions, including those related to the activity of 1810022C23Rik. By inhibiting Src kinases, Dasatinib can lead to the functional inhibition of related proteins, including 1810022C23Rik. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $26.00 $119.00 $213.00 | 27 | |
Imatinib is a tyrosine kinase inhibitor that targets Bcr-Abl, c-Kit, and PDGFR. Proteins like 1810022C23Rik, which may be regulated by these kinases, will experience functional inhibition as a result of Imatinib's action on these targets. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Rapamycin inhibits the mammalian target of rapamycin (mTOR), a central regulator of cell growth and proliferation. Inhibition of mTOR can lead to the functional inhibition of downstream proteins that are regulated by mTOR signaling pathways, potentially including proteins similar to 1810022C23Rik. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
Sorafenib is a multikinase inhibitor that targets Raf kinases, VEGFR, and PDGFR. By inhibiting these kinases, Sorafenib disrupts signaling pathways that regulate cellular proliferation, angiogenesis, and apoptosis, which can lead to the functional inhibition of proteins like 1810022C23Rik that are regulated by these pathways. | ||||||