Date published: 2025-11-1

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ELSPBP1 Inhibitors

ELSPBP1 inhibitors are a class of chemical compounds that interact with various signaling pathways and biological processes to indirectly inhibit the functional activity of the ELSPBP1 protein. These inhibitors achieve this by targeting proteins and enzymes that play a crucial role in the pathways where ELSPBP1 is known to be involved. For instance, Staurosporine, a kinase inhibitor, has a broad target range but notably inhibits protein kinase C (PKC), which is a key player in the signaling cascade that influences ELSPBP1's activities. The inhibition of PKC by Staurosporine consequently leads to a decrease in ELSPBP1's functional activities. LY294002 and Wortmannin are both inhibitors of PI3K, which is an upstream regulator of the Akt signaling pathway. By inhibiting PI3K, these compounds reduce Akt activity, which is pivotal for cell survival and proliferation signals where ELSPBP1 is implicated. Consequently, ELSPBP1's role in mediating these signals is diminished.

Further, compounds like U0126 and PD98059 target the MAPK/ERK pathway by inhibiting MEK1/2, which is essential for the transmission of signals within this pathway, affecting ELSPBP1's capacity to participate in signal transduction. Similarly, SB203580 and SP600125 inhibit p38 MAPK and JNK, respectively, which are involved in the cellular stress response and apoptosis, processes in which ELSPBP1 is potentially active. By blocking these kinases, the inhibitors impair the pathways' function, leading to decreased activity of ELSPBP1 in these contexts. Moreover, LFM-A13, which inhibits Bruton's tyrosine kinase (BTK), and NSC 23766, which inhibits Rac1, disrupt B-cell receptor signaling and cytoskeletal reorganization, respectively.

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