EURL inhibitors are a class of chemical compounds that specifically target the EURL (Elongator Acetyltransferase Complex Subunit 1-like) protein. EURL is a member of the Elongator complex, a multi-protein complex involved in various cellular processes, including tRNA modification, transcriptional elongation, and histone acetylation. EURL, in particular, plays a role in stabilizing the Elongator complex and facilitating its functions, which are crucial for proper gene expression and the post-transcriptional modification of tRNAs. By inhibiting EURL, these compounds interfere with the stability and activity of the Elongator complex, potentially disrupting its ability to regulate gene expression and modify tRNAs. This inhibition affects key cellular processes, including protein synthesis and the maintenance of gene expression fidelity.
Inhibition of EURL has broader effects on cellular function, particularly in processes that depend on accurate tRNA modification and transcriptional regulation. The Elongator complex, with EURL as a critical component, is essential for the modification of specific uridines in tRNA, which ensures proper codon recognition during translation. By targeting EURL, inhibitors can impair this modification, leading to translational errors and misregulation of protein synthesis. Additionally, since the Elongator complex is involved in transcriptional elongation and histone acetylation, the inhibition of EURL can disrupt chromatin structure and transcriptional control, affecting gene expression at multiple levels. These inhibitors provide valuable tools for exploring the role of EURL and the Elongator complex in cellular homeostasis and gene regulation, shedding light on the complex mechanisms that maintain cellular function through tRNA modification and chromatin remodeling.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $186.00 $707.00 | 88 | |
Y-27632 is a ROCK inhibitor, affecting cytoskeletal dynamics, which might indirectly influence the function of C21orf91 if it's involved in these processes. | ||||||
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 | $152.00 $479.00 $632.00 $1223.00 $2132.00 | 33 | |
Trichostatin A, an HDAC inhibitor, alters chromatin structure and gene expression, potentially impacting C21orf91 expression or function. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine, a DNA methyltransferase inhibitor, alters gene expression patterns, which could indirectly influence C21orf91. | ||||||
SB 431542 | 301836-41-9 | sc-204265 sc-204265A sc-204265B | 1 mg 10 mg 25 mg | $82.00 $216.00 $416.00 | 48 | |
SB431542 is an inhibitor of the TGF-beta receptor, affecting cellular differentiation and proliferation, possibly influencing C21orf91. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
LY294002 is a PI3K inhibitor, impacting cell survival and metabolism, potentially influencing C21orf91 activity. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
PD98059 is an inhibitor of MEK, affecting the MAPK/ERK pathway, which could indirectly influence C21orf91. | ||||||
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 | |
MG132 is a proteasome inhibitor, which can affect protein degradation pathways, potentially influencing C21orf91. | ||||||
Bafilomycin A1 | 88899-55-2 | sc-201550 sc-201550A sc-201550B sc-201550C | 100 µg 1 mg 5 mg 10 mg | $98.00 $255.00 $765.00 $1457.00 | 280 | |
Bafilomycin A1, an inhibitor of the V-ATPase, affects lysosomal acidification and autophagy, potentially impacting C21orf91. | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $136.00 $446.00 | 114 | |
Thapsigargin disrupts calcium homeostasis in the endoplasmic reticulum, which could indirectly influence C21orf91. | ||||||