SFRS17B inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the SFRS17B protein, a member of the serine/arginine-rich splicing factor family. These proteins play a crucial role in the regulation of alternative splicing, a process by which precursor messenger RNA (pre-mRNA) is differentially spliced to generate multiple mRNA variants from a single gene. SFRS17B is known for its involvement in recognizing specific splice sites and influencing spliceosome assembly, thereby controlling the production of various protein isoforms. By inhibiting SFRS17B, these compounds can disrupt its regulatory functions in splicing, leading to changes in the splicing patterns of target genes. This modulation can result in alterations to gene expression, impacting cellular processes that rely on specific protein isoforms.
The structural design of SFRS17B inhibitors typically involves a deep understanding of the RNA-binding domains and the splicing-regulatory motifs of the SFRS17B protein. These inhibitors often bind to critical regions of the protein, such as its RNA recognition motifs (RRMs) or arginine/serine-rich (RS) domains, which are responsible for interacting with RNA and other splicing factors. The specificity of these inhibitors for SFRS17B is important to avoid unintended effects on other members of the serine/arginine-rich family, which share similar structural features. Researchers design these compounds to selectively interact with SFRS17B's unique domains, thereby preventing its normal function in the splicing machinery. SFRS17B inhibitors provide valuable tools for studying the mechanisms of alternative splicing regulation, enabling a deeper understanding of how splicing factors control gene expression and contribute to the complexity of cellular function.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
H-89 dihydrochloride | 130964-39-5 | sc-3537 sc-3537A | 1 mg 10 mg | $94.00 $186.00 | 71 | |
A potent inhibitor of protein kinase A (PKA), potentially disrupting AKAP17B-mediated localization and signaling. | ||||||
KT 5720 | 108068-98-0 | sc-3538 sc-3538A sc-3538B | 50 µg 100 µg 500 µg | $138.00 $220.00 $972.00 | 47 | |
Another PKA inhibitor, which could indirectly modulate the effects of AKAP17B on cellular signaling processes. | ||||||
Salbutamol | 18559-94-9 | sc-253527 sc-253527A | 25 mg 50 mg | $94.00 $141.00 | ||
A PKA inhibitor that acts as a cAMP antagonist, potentially affecting AKAP17B-associated signaling pathways. | ||||||
Gö 6976 | 136194-77-9 | sc-221684 | 500 µg | $227.00 | 8 | |
A protein kinase C (PKC) inhibitor, which could indirectly influence AKAP17B signaling pathways. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
A PI3K inhibitor, potentially modulating signaling pathways that interact with or are regulated by AKAP17B. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
A MEK inhibitor, which could affect the ERK/MAPK signaling pathway, potentially interacting with AKAP17B-regulated processes. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
A p38 MAPK inhibitor, potentially modulating stress responses that AKAP17B may be involved in. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $186.00 $707.00 | 88 | |
A ROCK inhibitor, which could affect cytoskeleton organization and cellular processes influenced by AKAP17B. | ||||||
ML-7 hydrochloride | 110448-33-4 | sc-200557 sc-200557A | 10 mg 50 mg | $91.00 $267.00 | 13 | |
An inhibitor of myosin light chain kinase (MLCK), potentially affecting cellular processes where AKAP17B is involved. | ||||||
Cilostamide (OPC 3689) | 68550-75-4 | sc-201180 sc-201180A | 5 mg 25 mg | $92.00 $357.00 | 16 | |
A phosphodiesterase 3 (PDE3) inhibitor, increasing cAMP levels and indirectly influencing AKAP17B-related PKA signaling. | ||||||