Sbpl inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the Sbpl protein, a member of the Split Ends (Spen) family of proteins. These proteins are involved in transcriptional regulation, playing key roles in gene expression by interacting with RNA and various transcription factors. Sbpl is known for its role in modulating transcription through its interaction with Notch signaling pathways and other regulatory proteins involved in gene silencing and activation. By inhibiting Sbpl, these compounds can disrupt its ability to influence gene transcription, leading to changes in the regulation of target genes and impacting downstream cellular processes dependent on precise transcriptional control.
The design of Sbpl inhibitors requires an understanding of the protein's structural domains, particularly the RNA recognition motifs (RRMs) and Spen paralog and ortholog C-terminal (SPOC) domains, which are critical for Sbpl's role in binding RNA and other transcriptional regulators. These inhibitors typically work by binding to these regions, preventing Sbpl from interacting with its target molecules. This inhibition can block the protein's function in transcriptional repression or activation, depending on the specific context of gene regulation. Researchers focus on creating inhibitors that are highly selective for Sbpl, as it shares structural features with other Spen family proteins. This selectivity is achieved through structural studies and molecular docking techniques to design compounds that precisely target Sbpl's unique domains. Sbpl inhibitors are valuable tools for studying transcriptional regulation, providing insights into how Sbpl and related proteins control gene expression and contribute to complex cellular signaling networks.
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Difluoromethylornithine | 70052-12-9 | sc-204723 sc-204723A sc-204723B sc-204723C sc-204723D sc-204723E | 10 mg 25 mg 100 mg 250 mg 1 g 5 g | $58.00 $130.00 $158.00 $311.00 $964.00 $4726.00 | 2 | |
An irreversible inhibitor of ornithine decarboxylase, the first enzyme in the polyamine biosynthesis pathway, reducing spermine levels and potentially influencing spermine binding proteins. | ||||||
Methylglyoxal solution | 78-98-8 | sc-250394 sc-250394A sc-250394B sc-250394C sc-250394D | 25 ml 100 ml 250 ml 500 ml 1 L | $143.00 $428.00 $469.00 $739.00 $1418.00 | 3 | |
A byproduct of glycolysis known to modify arginine residues in proteins and potentially alter spermine binding sites. | ||||||
Pentamidine | 100-33-4 | sc-208158 sc-208158A | 25 mg 50 mg | $373.00 $557.00 | ||
Indirectly affects spermine binding proteins by disrupting polyamine biosynthesis and function within cells. | ||||||
Spermidine | 124-20-9 | sc-215900 sc-215900B sc-215900A | 1 g 25 g 5 g | $56.00 $595.00 $173.00 | ||
While not an inhibitor, spermidine competes with spermine for binding sites, potentially modulating the activity of spermine binding proteins. | ||||||