Date published: 2025-11-1

1-800-457-3801

SCBT Portrait Logo
Seach Input

JMJD7-PLA2G4B Inhibitors

JMJD7-PLA2G4B inhibitors belong to a specialized category of chemical compounds designed to target and modulate the activity of two distinct proteins: JMJD7 and PLA2G4B. JMJD7, or Jumonji Domain-Containing Protein 7, is a member of the Jumonji-C domain-containing histone demethylase family, which plays a crucial role in epigenetic regulation by catalyzing the removal of methyl groups from histone proteins. PLA2G4B, or Phospholipase A2 Group IVB, is an enzyme involved in the hydrolysis of membrane phospholipids, releasing free fatty acids and lysophospholipids. These proteins have been implicated in various cellular processes, and inhibitors targeting both JMJD7 and PLA2G4B can have diverse effects on cellular signaling, lipid metabolism, and epigenetic regulation.

Structurally, JMJD7-PLA2G4B inhibitors are designed to interact with specific regions or binding sites on these proteins, preventing their normal catalytic activities. By inhibiting JMJD7, these compounds can influence histone methylation patterns, impacting gene expression and epigenetic regulation. Simultaneously, by inhibiting PLA2G4B, they can modulate lipid metabolism and the release of lipid signaling molecules, which are involved in various cellular processes. The study of JMJD7-PLA2G4B inhibitors is essential for gaining insights into the complex regulatory networks involving epigenetics and lipid metabolism, contributing to our broader understanding of cellular and molecular biology. These inhibitors serve as valuable tools for researchers investigating the roles of JMJD7 and PLA2G4B in cellular processes, offering opportunities to uncover novel connections between epigenetic regulation and lipid signaling pathways.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

MAFP

188404-10-6sc-203440
5 mg
$215.00
4
(1)

MAFP is an irreversible inhibitor that targets PLA2G4B's phospholipase A2 activity by covalently modifying the enzyme, preventing its action on phospholipids.

Manoalide

75088-80-1sc-200733
1 mg
$264.00
9
(1)

A marine natural product that inhibits PLA2G4B by covalently binding to its active site.

GSK J1

1373422-53-7sc-391113
sc-391113A
10 mg
50 mg
$189.00
$797.00
(0)

GSK-J1 is a JMJD3/UTX (histone demethylases) inhibitor. Given JMJD7's histone demethylase activity, this compound might indirectly influence the readthrough.

GSK-J4 Hydrochloride

1797983-09-5sc-490344
5 mg
$260.00
1
(0)

A more cell-permeable prodrug of GSK-J1. This compound might indirectly affect the JMJD7 component of the readthrough.