Chemical inhibitors of BC031181 include a range of compounds that target various kinases and signaling pathways which are crucial for the protein's activity. Staurosporine is a notable kinase inhibitor that can impede the phosphorylation processes essential to BC031181's function. By preventing these phosphorylation events, Staurosporine directly inhibits the activity of BC031181. Wortmannin and LY294002 both act as inhibitors of PI3K, a kinase that is central to several signaling pathways. By inhibiting PI3K, these compounds can reduce the phosphorylation of downstream proteins that are necessary for the proper functioning of BC031181, effectively leading to its functional inhibition. Rapamycin, by targeting the mTOR pathway, can influence the regulation of protein synthesis and cell growth, which are processes BC031181 may be involved in. By inhibiting this pathway, Rapamycin can decrease the functional activity of BC031181.
Further, PD98059 and U0126 target the MEK1/2 enzymes in the MAPK/ERK pathway, which is a common signaling route that BC031181 could utilize. By preventing the activation of this pathway, these inhibitors can reduce the activity of BC031181. SB203580 and SP600125 inhibit the p38 MAP kinase and JNK, respectively, which are part of stress-related signaling pathways that BC031181 may rely upon. By inhibiting these kinases, these compounds can reduce the activity of proteins regulated by the p38 MAPK and JNK pathways, including BC031181. Gefitinib and Erlotinib both inhibit EGFR tyrosine kinase, while Lapatinib inhibits both EGFR and HER2. These kinases, when inhibited, can prevent the activation of downstream signaling pathways necessary for the function of BC031181. Lastly, Triciribine targets Akt kinase, which is involved in cellular survival pathways. If BC031181 functions downstream of Akt, inhibition by Triciribine can lead to a decrease in BC031181 activity by blocking the survival signals that would normally upregulate it.
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