DDX17 inhibitors represent a diverse chemical class of compounds that target the DDX17 protein, a member of the DEAD box helicase family. These inhibitors are designed to interfere with the enzymatic activity of DDX17, which functions as an RNA helicase involved in various aspects of RNA metabolism, including RNA splicing, transcriptional regulation, and ribosome assembly. The chemical structures of DDX17 inhibitors can vary widely, encompassing both natural products and synthetic molecules. What unifies them is their ability to interact with specific regions of DDX17, disrupting its function and consequently impacting various cellular processes governed by this essential RNA helicase.
Structurally, DDX17 inhibitors often contain functional groups or motifs that enable them to bind to the active site or RNA-binding domains of the DDX17 protein. These interactions can occur through hydrogen bonding, van der Waals forces, or other non-covalent interactions. In some cases, co-crystallography studies have revealed the precise molecular interactions between DDX17 and its inhibitors. This structural information has facilitated the rational design of more potent and selective DDX17 inhibitors. DDX17 inhibitors have been instrumental in advancing our understanding of the role of DDX17 in cellular processes, particularly in RNA metabolism. Researchers have employed these inhibitors as valuable tools to probe the functional consequences of DDX17 inhibition, shedding light on its involvement in RNA processing. While DDX17 inhibitors hold promise for their research applications, their chemical diversity and specific mechanisms of action continue to be explored, offering further insights into the intricate world of RNA biology and its regulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
NSC-59984 | 803647-40-7 | sc-507310 | 10 mg | $230.00 | ||
NSC59984 is a small molecule compound that has been reported as an inhibitor of DDX17. It has shown potential in suppressing cancer cell growth by disrupting RNA processing. | ||||||
Ivermectin | 70288-86-7 | sc-203609 sc-203609A | 100 mg 1 g | $57.00 $77.00 | 2 | |
Ivermectin has been reported to have inhibitory effects on DDX17. | ||||||
BX 795 | 702675-74-9 | sc-281689 sc-281689A sc-281689C sc-281689B sc-281689D sc-281689E | 2 mg 5 mg 10 mg 25 mg 50 mg 100 mg | $219.00 $273.00 $331.00 $495.00 $882.00 $1489.00 | 5 | |
BX-795 is a compound known to inhibit multiple kinases, including DDX17. It has shown anti-proliferative effects in certain cancer cell lines by targeting DDX17. | ||||||
Pladienolide B | 445493-23-2 | sc-391691 sc-391691B sc-391691A sc-391691C sc-391691D sc-391691E | 0.5 mg 10 mg 20 mg 50 mg 100 mg 5 mg | $299.00 $5699.00 $11099.00 $25500.00 $66300.00 $2875.00 | 63 | |
Pladienolide B is a natural product compound that has been investigated as a DDX17 inhibitor. It interferes with RNA splicing and has potential anti-cancer properties. | ||||||
Herboxidiene | 142861-00-5 | sc-506378 | 1 mg | $1009.00 | ||
Herboxidiene is a product compound that has been reported to inhibit DDX17. It can disrupt RNA processing and has shown promise in cancer research. | ||||||
Platensimycin | 835876-32-9 | sc-202292 | 250 µg | $462.00 | 1 | |
Platensimycin has been found to inhibit DDX17. Its potential as an anti-cancer agent is under investigation. | ||||||
Kinetin | 525-79-1 | sc-207780 sc-207780A | 1 g 5 g | $38.00 $48.00 | ||
Kinetin is a plant hormone that has been studied for its DDX17 inhibitory effects. | ||||||
Cisplatin | 15663-27-1 | sc-200896 sc-200896A | 100 mg 500 mg | $138.00 $380.00 | 101 | |
Cisplatin has been reported to inhibit DDX17 activity, although it primarily acts through DNA damage. | ||||||
Toyocamycin | 606-58-6 | sc-362812 | 10 mg | $138.00 | ||
Toyocamycin is a nucleoside analog that has been shown to inhibit DDX17. It interferes with RNA processing and may have applications in cancer research. | ||||||