JMJD7 inhibitors belong to a specialized class of chemical compounds designed to target and modulate the activity of the Jumonji domain-containing protein 7 (JMJD7). The JMJD7 protein, part of the larger family of Jumonji domain-containing histone demethylases, plays a crucial role in cellular processes by regulating the demethylation of lysine residues on histone proteins. Histone demethylation is a key epigenetic modification that influences gene expression and chromatin remodeling. JMJD7, specifically, has been implicated in various biological functions, including transcriptional regulation, cell cycle progression, and DNA repair. As a result, the development of JMJD7 inhibitors represents a significant area of interest in the field of chemical biology and drug discovery.
JMJD7 inhibitors are carefully designed to selectively bind to the active site of the JMJD7 protein, thereby blocking its enzymatic activity. By inhibiting JMJD7, these compounds aim to modulate histone methylation levels and, consequently, influence the epigenetic landscape within cells. The rational design of JMJD7 inhibitors involves the optimization of chemical features to enhance binding affinity and specificity for the target protein. Researchers employ various structural and computational approaches to tailor these inhibitors, ensuring a high degree of selectivity while minimizing off-target effects
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
MAFP | 188404-10-6 | sc-203440 | 5 mg | $219.00 | 4 | |
Irreversible inhibitor that binds to the active site serine of PLA2s, preventing substrate access. | ||||||
Rosiglitazone | 122320-73-4 | sc-202795 sc-202795A sc-202795C sc-202795D sc-202795B | 25 mg 100 mg 500 mg 1 g 5 g | $120.00 $326.00 $634.00 $947.00 $1259.00 | 38 | |
PPARγ agonist that can alter PLA2 expression, potentially influencing PLA2G4B activity by modulating gene expression. | ||||||
Manoalide | 75088-80-1 | sc-200733 | 1 mg | $269.00 | 9 | |
Covalent modifier of PLA2, potentially affecting PLA2G4B by altering signal transduction pathways. | ||||||
ACEA | 220556-69-4 | sc-202902 sc-202902A | 5 mg 25 mg | $77.00 $306.00 | 3 | |
Inhibits cPLA2, possibly affecting PLA2G4B-mediated lipid signaling by reducing substrate availability. | ||||||