Date published: 2025-9-17

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BC031441 Inhibitors

Chemical inhibitors of BC031441 employ various mechanisms to impede its function. Staurosporine, a broad-spectrum protein kinase inhibitor, targets the ATP-binding sites of kinases, thereby preventing the phosphorylation events necessary for the activation of BC031441. Similarly, LY294002, which is a specific inhibitor of PI3K, disrupts the PI3K/Akt pathway, a signaling cascade that is often crucial for the activity of proteins like BC031441. By obstructing this pathway, LY294002 ensures that the downstream signaling necessary for BC031441's function is curtailed. Another inhibitor, Rapamycin, acts on mTOR, a kinase involved in cell growth and proliferation, to suppress the activation of targets that BC031441 may require for its function.

Further inhibitory actions include PD98059, which targets MEK1/2 and thereby inhibits the ERK/MAPK pathway, a signaling mechanism that can regulate the activity of BC031441. SB203580 takes a different approach by selectively inhibiting p38 MAP kinase, which may affect BC031441 if its activity or stability is contingent on this stress response pathway. Src family kinases, which can be involved in the activation of BC031441, are targeted by PP2, resulting in the inhibition of BC031441's functional activity. Dasatinib extends this approach by not only inhibiting Src family kinases but also Bcr-Abl, potentially blocking multiple pathways that BC031441 may utilize. Similarly, Sorafenib, a multi-kinase inhibitor, impedes RAF kinases, VEGFR, and PDGFR, which could be involved in the activation of BC031441. SP600125 and ZM447439 target the JNK and Aurora kinases, respectively, both of which could be integral to BC031441's function, particularly regarding stress response and cell cycle progression. Lastly, Lestaurtinib inhibits JAK2, affecting the JAK-STAT signaling pathway, and PD173074 inhibits FGFR, both potentially leading to inhibition of BC031441 by blocking critical signaling pathways it may depend on.

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