Date published: 2025-11-9

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LOC646066 Inhibitors

Chemical inhibitors of LOC646066 can modulate its activity through various intracellular signaling pathways. LY294002 and Wortmannin are both inhibitors of PI3K, an upstream regulator in the PI3K/AKT signaling pathway. This pathway is crucial for the phosphorylation and activation of downstream proteins, including LOC646066. By inhibiting PI3K, these chemicals prevent the activation of AKT, which in turn prevents the phosphorylation and activation of LOC646066, leading to its functional inhibition. Rapamycin, another inhibitor, targets mTOR, a key component further downstream in the PI3K/AKT/mTOR pathway. The inhibition of mTOR by Rapamycin results in a decrease in the functional activity of proteins regulated by this pathway, including LOC646066.

Further, U0126 and PD98059 focus on the MAPK/ERK pathway by specifically inhibiting MEK1/2, which is necessary for the activation of ERK. ERK is an upstream regulator of various proteins, including LOC646066. Inhibition of MEK1/2, therefore, leads to reduced activation of ERK and subsequent inhibition of LOC646066 activity. SB203580 and SP600125 inhibit p38 MAP kinase and JNK, respectively, which are part of alternative MAP kinase pathways that also regulate the activity of proteins like LOC646066. Bortezomib, a proteasome inhibitor, indirectly inhibits LOC646066 by preventing the degradation of regulatory proteins that exert an inhibitory control over LOC646066. Inhibitors like Gefitinib and Sorafenib target the EGFR and multiple kinases within signaling pathways that LOC646066 is a part of, reducing its activity through decreased pathway signaling. Lastly, Dasatinib and Imatinib inhibit Src family kinases and Bcr-Abl tyrosine kinase, respectively, which are involved in upstream signaling events required for LOC646066's activity. The inhibition of these kinases leads to a cessation of the signaling cascades necessary for LOC646066 activity, thus functionally inhibiting the protein.

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