DQX1 inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the DQX1 protein, which is part of the DEAH-box family of RNA helicases. DQX1 is an ATP-dependent RNA helicase that plays a vital role in unwinding RNA secondary structures, facilitating processes such as RNA splicing, ribosome biogenesis, and RNA decay. By regulating RNA remodeling, DQX1 influences critical cellular processes that are essential for the maintenance of RNA metabolism and gene expression. Inhibiting DQX1 provides researchers with an opportunity to study the precise role of RNA helicases in RNA processing, particularly in how RNA structure impacts transcription, translation, and post-transcriptional regulation.
The mechanism of DQX1 inhibitors typically involves binding to the ATP-binding domain or the RNA-binding domain of the DQX1 helicase, thereby preventing its ATPase activity and blocking its ability to unwind RNA duplexes. These inhibitors may be designed to mimic ATP or RNA substrates, allowing them to interfere with the protein's catalytic function. Alternatively, allosteric inhibitors might induce conformational changes in the helicase, reducing its efficiency or destabilizing the protein's functional conformation. Through the use of DQX1 inhibitors, researchers can explore how disruptions in RNA helicase activity affect RNA metabolism and how such disruptions influence the broader regulatory mechanisms governing gene expression. These inhibitors are important tools for understanding the role of RNA helicases in maintaining RNA integrity, splicing accuracy, and ribosome assembly, providing deeper insights into the molecular mechanisms that control RNA-mediated cellular functions.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
General kinase inhibitor that can affect various signal transduction pathways. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
MEK inhibitor that can disrupt the MAPK/ERK signaling pathway. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
PI3K inhibitor that can impair PI3K/Akt signaling pathway. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $92.00 $223.00 | 30 | |
Src family kinase inhibitor that can affect cell adhesion, growth, and differentiation signaling pathways. | ||||||
SB 431542 | 301836-41-9 | sc-204265 sc-204265A sc-204265B | 1 mg 10 mg 25 mg | $80.00 $212.00 $408.00 | 48 | |
TGF-β receptor inhibitor that can influence TGF-β signaling involved in cell proliferation and differentiation. | ||||||
PD173074 | 219580-11-7 | sc-202610 sc-202610A sc-202610B | 1 mg 5 mg 50 mg | $46.00 $140.00 $680.00 | 16 | |
FGFR inhibitor that can disrupt fibroblast growth factor signaling. | ||||||
IWP-2 | 686770-61-6 | sc-252928 sc-252928A | 5 mg 25 mg | $94.00 $286.00 | 27 | |
Wnt production inhibitor that can affect Wnt signaling pathway. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
mTOR inhibitor that can affect cell growth and autophagy pathways. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Proteasome inhibitor that can affect protein degradation and cell cycle progression. | ||||||
BML-275 | 866405-64-3 | sc-200689 sc-200689A | 5 mg 25 mg | $94.00 $348.00 | 69 | |
AMPK inhibitor that can influence cellular energy homeostasis. |