ANKRD39 inhibitors are a class of chemical compounds developed to target and interfere with the function of the ANKRD39 protein, which is part of the ankyrin repeat domain-containing family. ANKRD39, like other proteins in this family, contains multiple ankyrin repeat motifs, which are helical structures that facilitate protein-protein interactions by providing a stable binding interface. These repeats allow ANKRD39 to play a significant role in various cellular processes, including signaling pathways, protein trafficking, and structural organization. ANKRD39 inhibitors are designed to disrupt the protein's ability to participate in these processes by blocking its interaction with other proteins, thereby preventing the assembly or stabilization of protein complexes that rely on ANKRD39.
The chemical nature of ANKRD39 inhibitors can vary widely, ranging from small molecules to larger peptide-based compounds. These inhibitors typically act by binding to critical regions within the ankyrin repeat domains, such as hydrophobic cavities or charged surfaces that are essential for the protein's interaction with its partners. Some inhibitors are structured to mimic the natural ligands or binding partners of ANKRD39, competing for the same binding sites and effectively blocking the protein's normal function. Others work by inducing conformational changes in ANKRD39, destabilizing the repeat domains and hindering the protein's ability to maintain its functional structure. By interfering with the molecular interactions mediated by ANKRD39, these inhibitors serve as important tools for studying the protein's role in cellular mechanisms and gaining a deeper understanding of how ankyrin repeat domains contribute to the regulation of protein networks in 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 | $67.00 $223.00 $425.00 | 97 | |
PI3K inhibitor that can disrupt signal transduction, potentially affecting proteins regulated by the PI3K pathway. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $153.00 $396.00 | 113 | |
A broad-spectrum kinase inhibitor that can interfere with phosphorylation events and protein activation. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
An mTOR inhibitor that can modulate cellular growth and proliferation processes. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
Another PI3K inhibitor that can disrupt various signaling pathways, potentially affecting protein interactions. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
An inhibitor of the JNK signaling pathway, which can influence apoptosis and other cellular responses. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
A p38 MAPK inhibitor that could alter inflammatory response and cytokine production, affecting related proteins. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
An inhibitor of MEK, which can modulate the MAPK/ERK pathway and potentially affect proteins involved in this pathway. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $135.00 $1085.00 | 115 | |
A proteasome inhibitor that can affect protein degradation pathways, potentially influencing protein levels. | ||||||
Thalidomide | 50-35-1 | sc-201445 sc-201445A | 100 mg 500 mg | $111.00 $357.00 | 8 | |
A modulator of ubiquitin ligase activity, which can impact protein turnover and function. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $60.00 $265.00 $1000.00 | 163 | |
A proteasome inhibitor similar to Bortezomib, which can affect the degradation of a multitude of proteins. | ||||||