METTL2A inhibitors are a class of chemical compounds that specifically target and inhibit the enzymatic activity of the methyltransferase-like protein 2A (METTL2A). METTL2A is a member of the larger methyltransferase family, which plays a significant role in the methylation of nucleic acids and proteins. Methylation is a key post-translational modification that influences gene expression, protein interactions, and various cellular processes. METTL2A has been primarily associated with the methylation of RNA, contributing to the regulation of RNA metabolism, including its processing, stability, and translation efficiency. Inhibitors of METTL2A are designed to modulate its function by blocking its active site or interfering with its ability to transfer methyl groups to target molecules. The specificity of METTL2A inhibitors lies in their molecular interactions with the enzyme's catalytic domain, often through competitive or allosteric mechanisms.
The development of METTL2A inhibitors has provided valuable insights into the broader understanding of RNA methylation and its biological roles. By inhibiting METTL2A activity, researchers can dissect the specific contributions of RNA methylation in various cellular contexts, such as the regulation of gene expression and RNA splicing. Inhibitors in this chemical class often serve as molecular tools to explore the dynamics of methyltransferase activity within cells and to study the consequences of altered RNA methylation patterns. Additionally, METTL2A inhibitors can be utilized to study protein-protein and protein-RNA interactions governed by methylation status. Through structural and biochemical studies, the binding affinity and inhibition kinetics of these compounds have been characterized, contributing to a growing body of knowledge on how METTL2A functions within the broader methyltransferase family.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
Incorporates into RNA and DNA and inhibits methyltransferases by trapping them in a complex. | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $218.00 $322.00 $426.00 | 7 | |
A cytidine analog that targets DNA methyltransferases, reducing methylation levels. | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $131.00 $515.00 | 2 | |
Directly inhibits DNA methyltransferases, possibly affecting methylation patterns indirectly. | ||||||
Homocysteine | 6027-13-0 | sc-507315 | 250 mg | $195.00 | ||
A product inhibitor of various methyltransferases by competing with S-Adenosylmethionine. | ||||||
BIX01294 hydrochloride | 1392399-03-9 | sc-293525 sc-293525A sc-293525B | 1 mg 5 mg 25 mg | $37.00 $112.00 $408.00 | ||
Histone methyltransferase inhibitor that indirectly could affect RNA methylation by METTL2A. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $55.00 | 6 | |
Binds to GC-rich DNA sequences, potentially altering transcription and associated methylation. | ||||||
Folic Acid | 59-30-3 | sc-204758 | 10 g | $73.00 | 2 | |
Interfere with the methyl donor cycle, decreasing overall methylation capacity. | ||||||
Adenosine, periodate oxidized | 34240-05-6 | sc-214510 sc-214510A | 25 mg 100 mg | $119.00 $364.00 | ||
Inhibits S-adenosylhomocysteine hydrolase, thereby inhibiting transmethylation reactions. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
Modulates various signaling pathways and may indirectly influence methylation processes. | ||||||
Chaetocin | 28097-03-2 | sc-200893 | 200 µg | $126.00 | 5 | |
Specific inhibitor of histone methyltransferases, could have indirect effects on RNA methylation. | ||||||