Chemical inhibitors of the protein encoded by the gene 1700003E16Rik can exert their inhibitory effects through various mechanisms impacting the protein's activity. Wortmannin and LY294002 specifically target phosphoinositide 3-kinases, which are essential for the activation of the AKT signaling pathway. The protein encoded by 1700003E16Rik is a downstream effector in this pathway, and its functional activity is contingent upon phosphorylation events mediated by PI3K. By inhibiting PI3K, these compounds prevent the activation of AKT, leading to a decrease in the phosphorylation and activation of the 1700003E16Rik protein. Rapamycin, another inhibitor, acts by binding to FKBP12 and specifically inhibiting the mTOR complex 1, a crucial component in the PI3K/AKT/mTOR pathway. This inhibition disrupts the pathway at a point downstream of AKT, which in turn impacts the activity of the 1700003E16Rik protein.
Continuing with the theme of inhibiting key signaling pathways, Triciribine directly targets AKT, preventing its phosphorylation and subsequent activation. The activity of the 1700003E16Rik protein is dependent on these phosphorylation events, which are halted by Triciribine. U0126 and PD98059 exert their inhibitory effects on the mitogen-activated protein kinase (MAPK/ERK) pathway. They specifically inhibit MEK1/2, which are upstream of ERK, preventing the activation of this kinase cascade that may regulate the 1700003E16Rik protein. In a similar vein, SP600125 and SB203580 are inhibitors of the JNK and p38 MAP kinase pathways, respectively. By inhibiting these kinases, they interfere with the stress and cytokine response signaling pathways, which can regulate the activity of proteins like the one encoded by 1700003E16Rik. Erlotinib and Gefitinib inhibit the epidermal growth factor receptor tyrosine kinase, thereby disrupting downstream signaling that could affect the activity of the 1700003E16Rik protein. Staurosporine, being a broad-spectrum protein kinase inhibitor, impacts multiple kinases within the signaling pathways, potentially leading to the inhibition of the 1700003E16Rik protein. Lastly, Sorafenib targets various tyrosine protein kinases and RAF kinases within the MAPK pathway, which ultimately can disrupt the signaling cascade affecting the protein activity encoded by 1700003E16Rik.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $153.00 $396.00 | 113 | |
A potent inhibitor of many protein kinases. While it is broad-spectrum, Staurosporine may functionally inhibit 1700003E16Rik by inhibiting kinases within the relevant signaling pathways that lead to the activation of 1700003E16Rik. | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
Inhibits multiple tyrosine protein kinases, such as VEGFR and PDGFR, and also RAF kinases, which are part of the MAPK pathway. By inhibiting these kinases, Sorafenib disrupts signaling pathways that could lead to the functional inhibition of 170It seems there was a miscommunication; the table provided appears to be incomplete or not properly formatted, and no specific context was given to generate an accurate table. If you are looking to create a table of inhibitors and their potential effect on the gene 1700003E16Rik, please provide the correct details or context for the table. If you need help with creating tables or any other information, please let me know how I can assist you! | ||||||