Date published: 2025-9-18

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AU042671 Inhibitors

Chemical inhibitors of AU042671 can interfere with its function through various molecular pathways. Wortmannin and LY294002 are two such inhibitors that specifically target phosphoinositide 3-kinases (PI3K), which play a crucial role in the PI3K/AKT signaling pathway, a pathway that is essential for numerous cellular processes. By inhibiting PI3K, these chemicals prevent the subsequent activation of AKT, a kinase that, when phosphorylated, propagates downstream signaling events. This blockade can directly affect the activity of AU042671, assuming its function is regulated by the PI3K/AKT pathway. Similarly, Dasatinib acts on tyrosine kinases, including Src family kinases, which are part of a signaling cascade that could modulate the activity of AU042671. By inhibiting these kinases, Dasatinib can disrupt the phosphorylation state and consequently the function of downstream proteins, potentially including AU042671.

Other inhibitors target different aspects of cellular signaling networks. U0126 and PD98059 are selective for MEK1/2, key components of the MAPK/ERK pathway. Inhibition of MEK prevents the activation of ERK, which can have widespread effects on cellular functions that may involve AU042671. SB203580 specifically inhibits p38 MAP kinase, potentially affecting stress response elements that regulate the activity of AU042671. SP600125 targets the JNK pathway, another MAP kinase pathway, which can impact the function of AU042671 by disrupting its signaling processes. Additionally, Y-27632 inhibits ROCK kinases, which could affect the actin cytoskeleton and cellular motility that may be necessary for AU042671's function. Rapamycin inhibits mTOR, which is known to regulate protein synthesis and other critical cellular processes, and this inhibition could directly affect AU042671's activity. Staurosporine, being a broad-spectrum kinase inhibitor, could inhibit a wide range of kinases that phosphorylate AU042671, thus affecting its function. Finally, the proteasome inhibitors, Bortezomib and MG-132, can lead to an accumulation of misfolded proteins, disrupting the degradation pathway of proteins and potentially interfering with the normal functioning of AU042671 by affecting the cellular processes it is involved with.

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