Date published: 2025-9-16

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RBM45 Inhibitors

Chemical inhibitors of RBM45 include a range of molecules that target different cellular pathways, which can indirectly lead to the inhibition of this protein's function. Alsterpaullone and Roscovitine, both cyclin-dependent kinase inhibitors, work by disrupting the cell cycle regulation, a critical process where RBM45 is known to participate. By halting the cell cycle, these inhibitors can prevent RBM45 from carrying out its role in cell cycle checkpoints. Similarly, LY294002 and Wortmannin, which are phosphoinositide 3-kinase (PI3K) inhibitors, can interrupt signaling pathways that are essential for a variety of cellular functions, including RNA processing in which RBM45 is implicated. The disruption of PI3K signaling can lead to a functional inhibition of RBM45 by affecting its associated RNA processing activities.

Further down the signaling cascade, U0126 and SB203580 inhibit the MAPK/ERK and p38 MAPK pathways, respectively. By blocking these kinases, the inhibitors can affect the stress response mechanisms and RNA processing events within the cell, where RBM45 plays a vital role. Rapamycin's inhibition of the mTOR pathway can interfere with RBM45's involvement in regulating protein synthesis and RNA binding, as mTOR is a central regulator of cell growth and protein synthesis. Cycloheximide, which inhibits the translocation step in protein synthesis, can lead to a decreased formation of protein-RNA complexes that RBM45 is a part of, thereby inhibiting its function. Thapsigargin and Brefeldin A disrupt cellular homeostasis by targeting calcium signaling and protein transport, respectively, both of which are crucial for the proper functioning of RBM45 in RNA-protein complexes. MG132's proteasome inhibition can lead to an accumulation of aberrant proteins that can indirectly interfere with RBM45's role in RNA processing. Lastly, Actinomycin D binds to DNA and inhibits RNA polymerase activity, which can reduce the transcription of RNAs that interact with RBM45, thereby indirectly inhibiting RBM45's involvement in RNA metabolism and processing.

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