Date published: 2025-9-18

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C6orf162 Inhibitors

Chemical inhibitors of C6orf162 can act on various signaling pathways that this protein is involved in, thereby reducing its activity. Wortmannin is known to inhibit PI3K, which is instrumental in multiple signaling cascades; when PI3K is inhibited, subsequent AKT phosphorylation is decreased. As a consequence, if C6orf162 functions are associated with the PI3K/AKT pathway, its activity would be inhibited. Similarly, LY294002 is another PI3K inhibitor that prevents AKT activation, leading to potential suppression of C6orf162 if it is part of this signaling network. Triciribine specifically targets AKT, thereby inhibiting its action and possibly diminishing C6orf162 activity if it is downstream of AKT.

Additionally, Rapamycin inhibits mTOR, a central protein in cell growth and proliferation pathways. Since mTOR can affect a wide range of downstream proteins, the inhibition of mTOR could lead to a decrease in C6orf162 activity if it is implicated in these pathways. PD98059 and U0126 are both inhibitors of MEK, which is upstream of ERK in the MAPK/ERK pathway. If C6orf162 is regulated by this pathway, these inhibitors would suppress its activity by preventing ERK activation. SB203580 and SP600125 target p38 MAPK and JNK, respectively, which are other members of the MAPK family. The inhibition of these kinases would reduce C6orf162 activity if it is involved in stress response or other processes mediated by p38 MAPK or JNK. Moreover, Dasatinib and PP2 are inhibitors of the Src family kinases. If C6orf162 interacts with pathways under the control of Src family kinases, the activity of C6orf162 would be inhibited by these chemicals. Lastly, Go6983 is a broad-spectrum inhibitor of PKC, which plays a role in various cell signaling processes; inhibition of PKC can lead to reduced C6orf162 activity if it is part of PKC-regulated pathways. SL327, which also inhibits MEK, would further ensure the downregulation of ERK activity, and consequently, the activity of C6orf162 if it is a component of the MEK/ERK signaling pathway.

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