Date published: 2025-9-17

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BC030307 Inhibitors

Chemical inhibitors of BC030307 include a range of compounds that target various signaling pathways and enzymes which are essential for its function. Staurosporine is a potent protein kinase inhibitor that can impede the phosphorylation processes necessary for the function of BC030307. By blocking the activity of these kinases, Staurosporine can disrupt the cascade of events leading to the activation or stabilization of BC030307. Similarly, Wortmannin and LY294002 act as phosphoinositide 3-kinase (PI3K) inhibitors, preventing the PI3K pathway from initiating downstream signals crucial for BC030307's activity. Triciribine takes a more downstream approach by specifically targeting Akt, a key signaling molecule in the PI3K pathway, which results in the inhibition of further signaling required for BC030307's functional role.

Furthermore, Rapamycin inhibits the mTOR pathway, which is instrumental in protein synthesis and cell growth, potentially blocking the functional pathways that BC030307 may utilize. PD98059 and U0126 target MEK1/2, which are upstream of the MAPK/ERK pathway. Inhibition of this pathway can prevent the activation of BC030307 that relies on MAPK/ERK signaling for its function. SB203580 and SP600125 inhibit p38 MAP kinase and JNK, respectively, which can lead to the inhibition of BC030307 by stalling the necessary signaling through these specific pathways. Lastly, Gefitinib, Erlotinib, and Lapatinib are tyrosine kinase inhibitors that block EGFR and HER2, which could lead to inhibition of BC030307 by preventing signaling through pathways downstream of these receptors. These inhibitors collectively demonstrate a concerted effort to disrupt the signaling networks and pathways necessary for the function of BC030307 by obstructing the activity of key enzymes and receptors that facilitate its role within the cell.

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