Date published: 2025-10-27

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A930008G19Rik Inhibitors

Chemical inhibitors of A930008G19Rik can exert their inhibitory effects through various molecular mechanisms, impacting specific signaling pathways to reduce the protein's activity within cells. For instance, Wortmannin and LY294002 target phosphatidylinositol 3-kinase (PI3K), leading to a reduction in AKT phosphorylation-a process vital for A930008G19Rik activity in cell survival and metabolism. Similarly, Rapamycin binds to and inhibits the mechanistic target of rapamycin (mTOR), a kinase that plays a central role in regulating protein synthesis and cell growth, which is necessary for the proper functioning of A930008G19Rik. By inhibiting mTOR, Rapamycin can diminish the activity of A930008G19Rik, which is likely involved in these growth-related processes.

Further, PD98059 and U0126 inhibit MEK1/2, key enzymes in the MAPK/ERK pathway that are responsible for cell growth and differentiation signals that regulate A930008G19Rik function. SB203580 and SP600125 work by inhibiting p38 MAPK and JNK, respectively, thereby disrupting stress response signaling and other cellular processes that A930008G19Rik could be regulating. Dasatinib and PP2 inhibit Bcr-Abl and Src family kinases, which are part of signal transduction pathways that control cell growth and survival, where A930008G19Rik is active. Sorafenib targets multiple receptor tyrosine kinases that are upstream regulators of the pathways governing cell proliferation, in which A930008G19Rik operates. Lastly, Lapatinib inhibits EGFR and HER2, key receptors in pathways that regulate cell growth and survival, and Omipalisib, a dual PI3K/mTOR inhibitor, suppresses the activity of A930008G19Rik by disrupting the signaling pathways it is involved in. Each chemical inhibitor, by targeting distinct kinases and receptors, manages to reduce the functional activity of A930008G19Rik through a specific blockade of the pathways vital for its role within the cell.

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