Date published: 2025-11-24

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DUS3L Inhibitors

DUS3L inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the DUS3L protein, a member of the dual specificity phosphatase family. DUS3L, also known as dual specificity phosphatase-like 3, is involved in the regulation of cellular signaling pathways through its ability to dephosphorylate both tyrosine and serine/threonine residues on target proteins. This dual specificity allows DUS3L to play a critical role in modulating key signaling cascades, including those related to cell growth, differentiation, and stress responses. The precise function of DUS3L is not fully elucidated, but it is believed to be involved in fine-tuning the activity of mitogen-activated protein kinases (MAPKs) and other signaling molecules that are essential for maintaining cellular homeostasis. The inhibition of DUS3L by specific inhibitors typically involves the binding of these compounds to the enzyme's active site or other critical domains, preventing it from effectively interacting with its substrates. This inhibition disrupts DUS3L's ability to regulate phosphorylation states within key signaling pathways, leading to altered cellular responses. For example, inhibiting DUS3L could result in sustained phosphorylation of MAPKs or other downstream effectors, which might impact processes such as gene expression, cell cycle progression, and apoptosis. Additionally, DUS3L inhibitors may affect the broader network of signaling interactions within the cell, potentially influencing cellular responses to environmental stressors or changes in external growth signals. Understanding the effects of DUS3L inhibition provides valuable insights into the specific roles this phosphatase plays in cellular physiology, shedding light on how the regulation of phosphorylation states contributes to the dynamic control of cellular functions and the maintenance of overall cellular balance. This knowledge is essential for advancing our understanding of the molecular mechanisms that govern signaling networks and their impact on cell behavior.

Items 11 to 12 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Bortezomib

179324-69-7sc-217785
sc-217785A
2.5 mg
25 mg
$132.00
$1064.00
115
(2)

Bortezomib is a proteasome inhibitor that can cause the accumulation of misfolded proteins. This can lead to cellular stress responses that may include the degradation or mislocalization of DUS3L, indirectly inhibiting its function.

Thapsigargin

67526-95-8sc-24017
sc-24017A
1 mg
5 mg
$94.00
$349.00
114
(2)

Thapsigargin is a sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA) pump inhibitor that disrupts calcium homeostasis. Alteration in calcium signaling can indirectly inhibit DUS3L if its function is calcium-dependent or if it interacts with calcium-binding proteins.