Date published: 2025-9-20

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1700010D01Rik Inhibitors

Chemical inhibitors of 1700010D01Rik can interrupt various signaling pathways crucial for its activity. PD98059 and U0126 target the MEK1/2 enzymes within the MAPK/ERK pathway, a signaling route that can be essential for the activation or stability of 1700010D01Rik. The inhibition of MEK1/2 by these chemicals results in the disruption of downstream signaling that 1700010D01Rik may rely on for its function. Similarly, LY294002 and Wortmannin exert their effects by inhibiting PI3K, a key component of the PI3K/Akt pathway. Since PI3K is upstream of many cellular processes, these inhibitors can prevent the activation of 1700010D01Rik or destabilize complexes it is associated with. Rapamycin, through its inhibition of mTOR, can disrupt mTOR signaling, which might be a pathway regulating the function or expression of 1700010D01Rik.

In parallel, Y-27632 targets ROCK kinase within the Rho/ROCK pathway. The inhibition of ROCK can lead to the inhibition of 1700010D01Rik if it is involved in this pathway by altering the cytoskeletal arrangements that could influence the function of 1700010D01Rik. SB203580, by inhibiting p38 MAP kinase, disrupts a pathway that 1700010D01Rik may participate in, leading to its functional inhibition. Another inhibitor, SB431542, targets the TGF-β receptor, which can inhibit 1700010D01Rik by halting the downstream signaling cascade it might be part of. SP600125 inhibits JNK, an approach that can inhibit 1700010D01Rik by altering the JNK signaling pathways, which can be integral to the protein's role in the cell. PP2, through its inhibition of Src family kinases, can inhibit 1700010D01Rik by interfering with the signaling pathways regulated by these kinases, which may be vital for the functional activity of 1700010D01Rik. PD173074 inhibits FGFR, thereby potentially inhibiting 1700010D01Rik by altering the downstream signaling pathways that involve this protein. Lastly, Staurosporine is a broad-spectrum kinase inhibitor that can inhibit 1700010D01Rik by general disruption of kinase-dependent signaling pathways, which are likely to affect the functional activity of this particular protein.

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