Ubr4 inhibitors are a class of chemical compounds designed to target and modulate the activity of the Ubiquitin Protein Ligase E3 Component N-Recognin 4 (Ubr4) protein. Ubr4 is a large E3 ubiquitin ligase that plays a significant role in the ubiquitin-proteasome system (UPS), a cellular machinery responsible for protein degradation. Specifically, Ubr4 is involved in the N-end rule pathway, a branch of the UPS that recognizes and marks proteins for degradation based on the identity of their N-terminal amino acid. Ubr4 functions by attaching ubiquitin molecules to specific target proteins, thereby tagging them for proteasomal degradation. Inhibitors of Ubr4 are developed to interact with this E3 ligase, disrupting its ubiquitin ligase activity and affecting protein degradation pathways within the cell.
These inhibitors are typically small molecules or compounds designed to bind to Ubr4, interfering with its interactions with target proteins, ubiquitin-conjugating enzymes, or other regulatory components of the UPS. By doing so, Ubr4 inhibitors may affect the ubiquitination and subsequent degradation of specific proteins, leading to alterations in the cellular proteome. Research into Ubr4 inhibitors is essential for understanding the molecular mechanisms governing protein degradation and the role of Ubr4 in maintaining cellular protein homeostasis. Insights gained from studying Ubr4 inhibitors may contribute to a deeper understanding of protein quality control mechanisms within cells and their implications in various cellular processes.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
Camptothecin inhibits DNA topoisomerase I, potentially causing DNA damage and altering transcription, which might affect Ubr4 expression. | ||||||
Mitomycin C | 50-07-7 | sc-3514A sc-3514 sc-3514B | 2 mg 5 mg 10 mg | $65.00 $99.00 $140.00 | 85 | |
Mitomycin C forms DNA crosslinks, impairing DNA replication and transcription processes, which could reduce Ubr4 expression. | ||||||
Bleomycin | 11056-06-7 | sc-507293 | 5 mg | $270.00 | 5 | |
Bleomycin induces DNA breaks, potentially affecting transcription and reducing Ubr4 mRNA levels. | ||||||
(−)-α-Santonin | 481-06-1 | sc-252339 | 5 g | $106.00 | ||
α-Santonin can induce oxidative stress and might influence transcription factors, potentially decreasing the expression of Ubr4. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A is an inhibitor of histone deacetylases (HDACs), which might alter chromatin structure and Ubr4 expression. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Bortezomib inhibits the proteasome, potentially leading to feedback inhibition of proteins like Ubr4 due to proteotoxic stress. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Cycloheximide inhibits eukaryotic protein synthesis, potentially reducing Ubr4 protein levels by preventing translation. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $56.00 $260.00 $980.00 | 163 | |
MG132 inhibits proteasomes and can affect protein turnover, which might lead to altered Ubr4 expression through feedback mechanisms. | ||||||
Actinonin | 13434-13-4 | sc-201289 sc-201289B | 5 mg 10 mg | $160.00 $319.00 | 3 | |
Actinonin is a peptide deformylase inhibitor, which might affect the N-terminal modification of proteins and influence Ubr4 expression. | ||||||
Homoharringtonine | 26833-87-4 | sc-202652 sc-202652A sc-202652B | 1 mg 5 mg 10 mg | $51.00 $123.00 $178.00 | 11 | |
Homoharringtonine inhibits protein synthesis by preventing the initial elongation step of translation, potentially affecting Ubr4 levels. | ||||||