PRDM11 inhibitors belong to a class of chemical compounds designed to selectively target and modulate the activity of the PR domain zinc finger protein 11, abbreviated as PRDM11. PRDM11 is a transcription factor and a member of the PRDM (PRDI-BF1 and RIZ homology domain) family of proteins. These proteins play crucial roles in the regulation of gene expression during development and tissue differentiation. PRDM11, specifically, is known for its involvement in hematopoiesis, the process by which blood cells are formed. It plays a critical role in the specification of lymphoid progenitor cells, contributing to the development of various immune cell types, including T cells and natural killer (NK) cells. PRDM11 inhibitors are developed through chemical synthesis and structural optimization techniques, with the primary goal of interacting with specific domains or functional motifs of the PRDM11 protein to influence its transcriptional activity.
The design of PRDM11 inhibitors typically involves creating molecules that can selectively bind to PRDM11, disrupting its interactions with DNA or other transcriptional regulatory proteins. By modulating PRDM11 activity, these inhibitors can affect gene expression patterns, particularly those involved in the development and differentiation of immune cells. The study of PRDM11 inhibitors offers valuable insights into the intricate molecular mechanisms governing hematopoiesis and immune cell development, providing a deeper understanding of the fundamental processes that underlie the formation of the immune system. This research contributes to our knowledge of basic developmental biology and the regulatory networks that control immune cell fate and function.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
An autophagy inhibitor that can affect cellular stress responses and potentially modulate gene expression. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $56.00 $260.00 $980.00 | 163 | |
A proteasome inhibitor that can cause accumulation of regulatory proteins, possibly influencing PRDM11 expression. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
An inhibitor of DNA topoisomerase I, potentially affecting DNA replication and transcription processes. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
A DNA-binding antibiotic that can inhibit transcription factor binding, potentially decreasing PRDM11 expression. | ||||||
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 | |
A DNA methyltransferase inhibitor leading to demethylation of DNA and affecting gene expression. | ||||||
Alsterpaullone | 237430-03-4 | sc-202453 sc-202453A | 1 mg 5 mg | $67.00 $306.00 | 2 | |
A cyclin-dependent kinase inhibitor that may influence cell cycle-related gene expression. | ||||||
RO-3306 | 872573-93-8 | sc-358700 sc-358700A sc-358700B | 1 mg 5 mg 25 mg | $65.00 $160.00 $320.00 | 37 | |
An inhibitor of CDK1, leading to cell cycle arrest and changes in gene expression patterns. | ||||||
Etoposide (VP-16) | 33419-42-0 | sc-3512B sc-3512 sc-3512A | 10 mg 100 mg 500 mg | $32.00 $170.00 $385.00 | 63 | |
A topoisomerase II inhibitor that can lead to DNA damage and potentially alter gene expression patterns. | ||||||