Date published: 2025-11-7

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1700018P22Rik Inhibitors

Chemical inhibitors of 1700018P22Rik can interfere with its function through various mechanisms by targeting different signaling pathways and kinases. Staurosporine, a potent kinase inhibitor, can inhibit a broad spectrum of kinases involved in phosphorylation, which is a crucial regulatory process for proteins, including 1700018P22Rik. This inhibition can prevent essential phosphorylation events required for 1700018P22Rik's function. Similarly, Bisindolylmaleimide I, by specifically inhibiting Protein Kinase C (PKC), can disrupt the phosphorylation process if PKC-mediated phosphorylation is necessary for 1700018P22Rik's activity. LY294002 and Wortmannin, both phosphoinositide 3-kinases (PI3K) inhibitors, can block the PI3K/Akt pathway. If 1700018P22Rik is a part of this pathway, its activity would be inhibited due to the prevention of downstream signaling.

Furthermore, Rapamycin targets the mTOR signaling pathway, which is integral to cell growth and proliferation. Inhibition of mTOR can lead to reduced activity of 1700018P22Rik if it is linked to this pathway. U0126 and PD98059 are inhibitors of MEK1/2 and by inhibiting this kinase, they can decrease the activity of the ERK pathway, which, in turn, can inhibit 1700018P22Rik if it is a downstream effector. SB203580's inhibition of p38 MAP kinase can affect 1700018P22Rik if it is involved in stress response pathways reliant on p38 MAPK. Similarly, SP600125's inhibition of JNK can decrease 1700018P22Rik activity if JNK signaling regulates it. Lastly, Dasatinib and PP2, as Src family kinase inhibitors, can inhibit Src kinase signaling, leading to reduced 1700018P22Rik activity if Src kinases regulate it. ZM-447439's role as an Aurora kinase inhibitor can also affect 1700018P22Rik's function if it is involved in the cell cycle and dependent on Aurora kinase activity for its regulation.

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