M6A inhibitors are a class of chemical compounds that specifically target and inhibit the activity of proteins involved in the modification of RNA through N6-methyladenosine (m6A), one of the most common and well-characterized RNA modifications. The m6A modification occurs on adenosine bases within mRNA and is known to play a crucial role in regulating various aspects of RNA metabolism, including RNA stability, splicing, translation, and degradation. Proteins responsible for adding, recognizing, and removing m6A modifications are referred to as "writers," "readers," and "erasers," respectively. M6A writers, such as the METTL3-METTL14 complex, deposit the methyl group on adenosine, while readers, such as YTH-domain proteins, interpret the methylation signal to modulate RNA function. Inhibitors targeting these components can disrupt the m6A modification process, providing insights into how m6A regulates gene expression at the post-transcriptional level.
In research, m6A inhibitors are valuable tools for studying the complex role of RNA modifications in controlling gene expression and cellular function. By inhibiting the enzymes that install or interpret m6A marks, scientists can investigate how changes in m6A modification affect RNA processing, translation, and decay. This inhibition allows for the exploration of m6A's influence on cellular processes such as differentiation, cell growth, and stress responses. Additionally, m6A inhibitors can reveal how the m6A modification interacts with other RNA modifications and regulatory pathways, providing a clearer picture of the complex regulatory networks governing gene expression. Through the use of m6A inhibitors, researchers can gain a deeper understanding of the biological significance of RNA methylation and its contribution to various aspects of RNA biology and post-transcriptional regulation.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Lovastatin | 75330-75-5 | sc-200850 sc-200850A sc-200850B | 5 mg 25 mg 100 mg | $28.00 $88.00 $332.00 | 12 | |
that can affect lipid rafts, potentially influencing GPM6A's localization or function. | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $26.00 $92.00 $120.00 $310.00 $500.00 $908.00 $1821.00 | 46 | |
A tyrosine kinase inhibitor that can influence signaling pathways that may interact with GPM6A. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
PI3 kinase inhibitor which could modulate pathways related to GPM6A. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
ERK pathway inhibitor that can modulate signaling pathways possibly interacting with GPM6A. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
A PI3K inhibitor that may influence cellular pathways related to GPM6A. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
Rho-associated protein kinase (ROCK) inhibitor which might impact GPM6A related functions. | ||||||
Chelerythrine chloride | 3895-92-9 | sc-3547 sc-3547A | 5 mg 25 mg | $88.00 $311.00 | 17 | |
Protein kinase C inhibitor that could modulate pathways potentially interacting with GPM6A. | ||||||
KN-93 | 139298-40-1 | sc-202199 | 1 mg | $178.00 | 25 | |
Calmodulin-dependent protein kinase II inhibitor that may influence GPM6A related pathways. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
JNK inhibitor which may modulate signaling pathways related to GPM6A. | ||||||