Date published: 2025-11-4

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1110057K04Rik Inhibitors

Chemical inhibitors of 1110057K04Rik can intervene with its function by various modes of action, each specific to the inhibitor's target within the cell's signaling pathways. Staurosporine, a broad-spectrum kinase inhibitor, can obstruct several kinases that could be responsible for phosphorylating 1110057K04Rik, thereby impacting its activity. Similarly, Bisindolylmaleimide I, as a protein kinase C (PKC) inhibitor, can also impede the function of 1110057K04Rik if it is regulated by PKC-dependent signaling. LY294002 and Wortmannin, both phosphoinositide 3-kinases (PI3K) inhibitors, can disrupt PI3K-dependent pathways possibly associated with 1110057K04Rik's activity. The influence of these inhibitors underscores the pivotal role of kinase signaling in the regulation of 1110057K04Rik.

Furthermore, Rapamycin, by selectively inhibiting mTOR, can influence 1110057K04Rik's involvement in mTOR-dependent pathways. U0126 and PD98059, which target MEK1/2, can prevent the activation of ERK, potentially affecting 1110057K04Rik's function if it operates downstream of the MAPK/ERK pathway. SB203580, as a p38 MAP kinase inhibitor, can disrupt the p38 MAPK signaling pathway, which may be essential for the function of 1110057K04Rik. SP600125, which inhibits c-Jun N-terminal kinase (JNK), can prevent JNK-mediated signal transduction involving 1110057K04Rik. Dasatinib, with its broad-spectrum inhibition of tyrosine kinases, can block critical enzymes that could be involved in the activation or function of 1110057K04Rik. Finally, Lapatinib and PP2, by respectively targeting EGFR/HER2 and Src family tyrosine kinases, can affect the signaling events and pathways that regulate the function of 1110057K04Rik. Each inhibitor's action reflects the complexity of cell signaling and the multiple points at which 1110057K04Rik's function can be modulated.

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