Date published: 2025-9-21

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A230107C01Rik Inhibitors

Chemical inhibitors of A230107C01Rik function by engaging with specific signaling pathways and enzymes that are crucial for the protein's activity. Staurosporine, for example, is known to inhibit protein kinases broadly, which can lead to the inhibition of A230107C01Rik by blocking the phosphorylation processes that are necessary for its activation within kinase signaling cascades. Similarly, Bisindolylmaleimide I targets Protein Kinase C (PKC), which is integral in the signaling pathways that regulate A230107C01Rik's function. By inhibiting PKC, Bisindolylmaleimide I can reduce the activity of A230107C01Rik. H-89, another kinase inhibitor, focuses on Protein Kinase A (PKA) and is capable of diminishing the phosphorylation and subsequent activation of A230107C01Rik or its associated proteins.

Further along these lines, U73122 functions by inhibiting phospholipase C (PLC), a pivotal player in the signaling mechanisms that activate A230107C01Rik. By preventing PLC activity, U73122 effectively hampers A230107C01Rik function. LY294002 operates through the inhibition of phosphoinositide 3-kinases (PI3K), which participate in regulating A230107C01Rik. PD98059 and SB203580 target the MAPK pathway at different points; PD98059 inhibits MEK, which is upstream of ERK and can regulate A230107C01Rik, while SB203580 specifically inhibits p38 MAPK, another kinase that impacts A230107C01Rik's signaling. SP600125's inhibition of c-Jun N-terminal kinase (JNK) also attenuates signaling pathways relevant for A230107C01Rik activity, leading to its functional inhibition. PP2 selectively inhibits Src family tyrosine kinases, which affect the regulation of A230107C01Rik, and Dasatinib provides broad-spectrum inhibition of tyrosine kinases like Bcr-Abl and Src family kinases, which are involved in the regulatory pathways of A230107C01Rik. Lapatinib's inhibition of the epidermal growth factor receptor (EGFR) and HER2, as well as Sorafenib's targeting of multiple receptor tyrosine kinases, disrupts signaling cascades that are crucial for A230107C01Rik's regulation and activity, thereby leading to functional inhibition of the protein.

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