PRDM15 inhibitors represent a specific group of chemical compounds designed to target and inhibit the activity of the PRDM15 protein, a member of the PRDM (PR domain-containing protein) family of transcription regulators. PRDM15 is characterized by its unique combination of a PR domain, which is related to the SET domain found in histone methyltransferases, and several zinc finger motifs. This protein plays a significant role in the regulation of gene expression, primarily through its involvement in chromatin remodeling and modification of histones. The activity of PRDM15 is pivotal in various cellular processes, including cell differentiation and development. The molecular structure of PRDM15, particularly its PR domain and zinc finger regions, is crucial for its interaction with chromatin and its subsequent transcription-regulating activity. The development of PRDM15 inhibitors focuses on these key functional domains, aiming to modulate the protein's role in gene expression.
The process of designing PRDM15 inhibitors is complex and multidisciplinary, involving a deep understanding of the protein's structure and function at the molecular level. These inhibitors are generally small molecules or peptides that specifically target the active sites or key structural domains of PRDM15, such as the PR domain or the zinc finger motifs. The development of these inhibitors requires detailed knowledge of PRDM15's three-dimensional structure, typically obtained through advanced techniques like X-ray crystallography or nuclear magnetic resonance (NMR) spectroscopy. These structural insights are crucial for identifying binding sites for inhibitors and for understanding the conformational dynamics of the protein. Complementing these experimental approaches, computational methods such as molecular docking and virtual screening are employed to predict the interactions between inhibitors and PRDM15. These predictions aid in the design and synthesis of compounds that are likely to exhibit high specificity and efficacy in binding to PRDM15. The development of PRDM15 inhibitors is an iterative process, involving the synthesis, testing, and refinement of compounds to achieve optimal inhibition. This field continues to advance with ongoing research and technological improvements, contributing to a broader understanding of the regulation of gene expression and the modulation of transcription factors.
SEE ALSO...
Items 1 to 10 of 11 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
Similar to 5-Azacytidine, it is used to inhibit DNA methyltransferase, which could lead to gene expression changes. | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
HDAC inhibitor that changes chromatin structure and potentially affects the transcription of various genes. | ||||||
Panobinostat | 404950-80-7 | sc-208148 | 10 mg | $196.00 | 9 | |
A potent HDAC inhibitor that can alter epigenetic regulation of gene expression. | ||||||
Chidamide | 743420-02-2 | sc-364462 sc-364462A sc-364462B | 1 mg 5 mg 25 mg | $61.00 $245.00 $1173.00 | ||
Disrupts the structure of the chromatin and can thereby influence gene expression. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
Binds to DNA and has been shown to affect gene expression by interfering with transcription factor binding. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
A diterpene triepoxide that has been shown to inhibit RNA polymerase II-mediated transcription. | ||||||
Histone Lysine Methyltransferase Inhibitor Inhibitor | 935693-62-2 free base | sc-202651 | 5 mg | $148.00 | 4 | |
A histone methyltransferase inhibitor which may alter methylation status and gene expression. | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $128.00 $505.00 | 2 | |
A non-nucleoside DNA methyltransferase inhibitor, which potentially leads to changes in gene expression profiles. | ||||||
Homocysteine | 6027-13-0 | sc-507315 | 250 mg | $195.00 | ||
A product inhibitor of methyltransferases that may affect epigenetic regulation. | ||||||
MS-275 | 209783-80-2 | sc-279455 sc-279455A sc-279455B | 1 mg 5 mg 25 mg | $24.00 $88.00 $208.00 | 24 | |
Selective HDAC inhibitor that can modulate gene expression through epigenetic remodeling. | ||||||