Date published: 2025-9-14

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ZNF763 Inhibitors

Chemical inhibitors of ZNF763 function through various mechanisms that affect different pathways and cellular processes. For instance, A-443654 and GSK690693 target the Akt pathway, a crucial signaling route that influences numerous cellular functions, including those associated with ZNF763. By inhibiting Akt, these chemicals prevent the phosphorylation of downstream substrates and transcription factors, which are essential for the functional activity of ZNF763. Similarly, LY294002, a PI3K inhibitor, acts upstream of Akt, leading to reduced Akt activity and subsequent diminishment of ZNF763 functionality. PF-4708671 specifically inhibits S6 Kinase 1, which operates downstream of the mTOR pathway. The mTOR pathway is integral to protein synthesis and cell growth, and by hindering S6K1, PF-4708671 indirectly hampers the cellular processes vital for ZNF763's functions.

Furthermore, the MEK inhibitors PD98059 and U0126 attenuate the MAPK/ERK signaling pathway, which could be involved in regulating the activity of ZNF763. By reducing ERK pathway signaling, these inhibitors may limit the activation of transcription factors that govern ZNF763's activity. Alsterpaullone targets cyclin-dependent kinases, which are pivotal in cell cycle control, thus potentially inhibiting ZNF763 by altering the phosphorylation state of proteins that regulate its function. MG132, a proteasome inhibitor, causes an accumulation of ubiquitinated proteins which can interfere with the normal protein degradation process, possibly leading to an indirect inhibition of ZNF763 activity. Additionally, chemicals like SB203580 and SP600125 target other MAP kinases such as p38 and JNK, respectively. These kinases are part of stress response pathways and can affect transcriptional regulation, which may be necessary for ZNF763's proper function. Lastly, Y-27632 inhibits ROCK, which can disrupt the actin cytoskeleton organization and thus potentially interfere with the cellular infrastructure required for ZNF763's activity, while Rapamycin inhibits mTOR, thereby suppressing cell growth and protein synthesis processes crucial for ZNF763.

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