Date published: 2025-9-13

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BC025816 Inhibitors

Chemical inhibitors of BC025816 can be understood through their action on various cellular signaling pathways and processes that are essential for the protein's function. Staurosporine serves as an archetypal kinase inhibitor, known to impede a diverse array of protein kinases. This can lead to the functional inhibition of BC025816 by obstructing its potential phosphorylation or activation, which may be mediated by these kinases. Similarly, both Wortmannin and LY294002 target the PI3K/Akt pathway. By inhibiting PI3K, these chemicals prevent the activation of downstream signaling that includes Akt, a kinase that may be essential for BC025816's function. The inhibition of this pathway can lead to a reduction in BC025816's activity, particularly if it relies on Akt-mediated phosphorylation for its function.

Moreover, Rapamycin is a well-known inhibitor of the mTOR pathway, which is a central regulator of cell growth and survival. By inhibiting mTOR, Rapamycin can lead to the inhibition of BC025816 if the protein is involved in mTOR-mediated processes. Triciribine directly inhibits Akt, which also results in the functional inhibition of BC025816 by halting the kinase activity of Akt. PD98059 and U0126, both selective inhibitors of MEK, target the MAPK/ERK pathway. By preventing the activation of this pathway, these inhibitors can decrease the activity of BC025816, presuming it has a role in the MAPK/ERK signaling. In parallel, SP600125 and SB203580 interfere with the JNK and p38 MAPK pathways, respectively. SP600125 inhibits JNK, which may be involved in BC025816's activity, particularly under stress responses, while SB203580 inhibits p38 MAPK, which could be integral to BC025816's role in inflammation or differentiation. Lestaurtinib and AG490, both JAK2 inhibitors, disrupt the JAK/STAT signaling pathway. The inhibition of this pathway by these chemicals may reduce BC025816 activity if it is implicated in processes governed by JAK/STAT signaling. Lastly, ZM447439 targets Aurora kinases, which are essential for cell cycle progression. By disrupting these kinases, ZM447439 can inhibit BC025816 if the protein plays a part in cell division or other processes linked to the Aurora kinase activity.

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