Date published: 2025-9-23

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4930471M23Rik Inhibitors

Chemical inhibitors of 4930471M23Rik can act through various mechanisms to inhibit its activity. Staurosporine, a potent protein kinase inhibitor, can block essential protein kinases that are vital for the activation of 4930471M23Rik, thus directly reducing its functional activity. LY294002 operates by inhibiting PI3K, which is a critical upstream regulator of AKT phosphorylation. Since AKT phosphorylation is a necessary step for numerous proteins to become fully active, the inhibition by LY294002 can lead to a reduction in the activity of 4930471M23Rik by limiting its phosphorylation state. Similarly, PD98059 targets MEK, a kinase upstream of ERK; by inhibiting MEK, the subsequent activation of ERK is reduced, which can result in a decrease in 4930471M23Rik activity if ERK phosphorylation is required for its full activation. SB203580, which selectively inhibits p38 MAP kinase, could diminish the overall functional capacity of 4930471M23Rik by limiting the activity of this signaling pathway, while SP600125 inhibits JNK, another kinase that, when inhibited, can result in reduced activity of 4930471M23Rik if JNK is involved in its activation process.

Additionally, Rapamycin inhibits mTOR, which is an integral component of multiple signaling pathways, potentially leading to a decrease in 4930471M23Rik activity. The irreversible inhibition of EGFR kinase by WZ4002 also presents a method to decrease the activity of downstream proteins such as 4930471M23Rik. PF-4708671 selectively targets p70 S6 kinase, which is part of the mTOR/S6K pathway; inhibition of this kinase can therefore inhibit the activity of 4930471M23Rik if it is part of this pathway. Y-27632 inhibits the Rho-associated kinase (ROCK), leading to reduced activity of downstream proteins like 4930471M23Rik, assuming ROCK signaling is implicated in its functionality. U0126, like PD98059, inhibits MEK and, by extension, could inhibit ERK activation, potentially leading to diminished 4930471M23Rik activity. Lastly, Bafilomycin A1 inhibits V-ATPase, an enzyme that acidifies intracellular vesicles; the inhibition of this enzyme can result in altered vesicular trafficking and pH, which can inhibit the activity of 4930471M23Rik if its function is pH-dependent.

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