RNK, also known as RNA kinase, is an enzyme involved in the phosphorylation of RNA molecules and plays a crucial role in regulating various cellular processes, including RNA metabolism and translation. RNK inhibitors belong to a class of chemical compounds designed to selectively target and inhibit the activity of RNA kinase, an enzyme involved in the phosphorylation of RNA molecules in cells. By interfering with the function of RNK, these inhibitors disrupt the process of RNA phosphorylation, leading to potential impacts on cellular RNA metabolism, translation, and other RNA-dependent processes. RNK inhibitors can encompass a variety of natural and synthetic compounds, each with its distinct mechanism of action.
Natural product inhibitors, such as staurosporine and rottlerin, are known to exhibit broad inhibitory effects on various kinases, including RNA kinase. Synthetic nucleotide analogues can also function as inhibitors by competing with natural nucleotides during RNA phosphorylation processes. Additionally, genetic approaches, such as RNA interference using siRNA molecules or CRISPR-Cas gene editing, may be utilized to target and reduce the expression of RNK genes, leading to inhibition of RNA kinase activity. Researchers employ various methods, including rational drug design, high-throughput screening, and structure-guided drug discovery, to identify novel RNK inhibitors and explore their potential as research tools to study cellular RNA metabolism and regulation. Additionally, understanding the interactions between RNA kinase and other proteins involved in RNA phosphorylation is essential for developing inhibitors that specifically disrupt these interactions. It's essential to acknowledge that the field of RNK inhibitors is an area of ongoing research and development, and specific details on individual compounds may vary.
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Fluorouracil | 51-21-8 | sc-29060 sc-29060A | 1 g 5 g | $36.00 $149.00 | 11 | |
5-FU is an antimetabolite chemotherapy drug that can inhibit RNA kinase activity, interfering with RNA phosphorylation and affecting RNA metabolism in cells. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
Staurosporine is a natural product with broad inhibitory effects on various kinases, including RNA kinase, thereby impacting cellular processes related to RNA. | ||||||
Rottlerin | 82-08-6 | sc-3550 sc-3550B sc-3550A sc-3550C sc-3550D sc-3550E | 10 mg 25 mg 50 mg 1 g 5 g 20 g | $82.00 $163.00 $296.00 $2050.00 $5110.00 $16330.00 | 51 | |
Rottlerin is another natural product known to inhibit RNA kinase activity, modulating RNA phosphorylation and related cellular functions. |