RUNDC2A inhibitors represent a relatively specific class of chemical compounds that target the RUN domain-containing protein 2A (RUNDC2A), a protein that plays a crucial role in cellular signaling and regulation of intracellular processes. The RUN domain, an acronym for RPIP8, UNC-14, and NESCA, is a protein structural motif associated with microtubule organization and intracellular trafficking, commonly seen in proteins involved in membrane dynamics and signal transduction pathways. RUNDC2A is primarily characterized by its association with the regulation of cytoskeletal dynamics and protein-protein interactions. These inhibitors are designed to disrupt the normal functional interactions of RUNDC2A, interfering with the signaling mechanisms mediated by this protein. By inhibiting the RUNDC2A, researchers can explore its role in modulating pathways that contribute to a broad range of cellular processes, including cell motility, division, and structural organization.
RUNDC2A inhibitors are typically characterized by their specific binding affinities to the RUN domain, and their molecular structures are designed to interfere with protein conformations required for RUNDC2A activity. These inhibitors have potential utility in studies aiming to understand RUNDC2A's role in various cellular and biochemical pathways. Additionally, these compounds provide valuable insights into the structural and functional consequences of RUN domain disruption, revealing the importance of RUNDC2A in the stabilization of intracellular transport systems and protein interactions. Chemically, these inhibitors may exhibit a wide variety of scaffolds, from small organic molecules to more complex heterocyclic systems, often tailored to ensure selectivity and potency. Advanced computational techniques and structure-activity relationship studies frequently contribute to the design and refinement of RUNDC2A inhibitors, enabling a more nuanced understanding of their molecular interactions within the cell.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Inhibits PI3K, a kinase upstream in pathways that may regulate RUNDC2A, leading to altered localization and function. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
Another PI3K inhibitor, preventing activation of downstream targets that can interact with RUNDC2A, modifying its activity. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
Inhibits MEK, which is part of the MAPK/ERK pathway, potentially altering RUNDC2A phosphorylation and its associated processes. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
Targets p38 MAPK, potentially affecting RUNDC2A's role in stress response pathways by altering phosphorylation patterns. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
Inhibits JNK, which may modify RUNDC2A activity through stress-related signaling pathways. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Inhibits mTOR, which can regulate RUNDC2A function by impacting protein synthesis and cell growth pathways. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
Inhibits MEK, potentially affecting RUNDC2A's interaction with proteins in the MAPK/ERK pathway. | ||||||
PP 2 | 172889-27-9 | sc-202769 sc-202769A | 1 mg 5 mg | $92.00 $223.00 | 30 | |
Inhibits Src family kinases, possibly altering RUNDC2A activity by changing kinase signaling pathways. | ||||||
LFM-A13 | 62004-35-7 | sc-203623 sc-203623A | 10 mg 50 mg | $119.00 $670.00 | ||
Inhibits Bruton's tyrosine kinase, which may modulate RUNDC2A function by affecting B cell receptor signaling. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Inhibits the proteasome, possibly leading to an accumulation of proteins that can bind and sequester RUNDC2A. | ||||||