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RJG-2036

Chemical Structure : RJG-2036

CAS No.: 2851993-73-0

RJG-2036 (RJG2036)

Catalog No.: PC-24626Not For Human Use, Lab Use Only.

RJG-2036 is a potent, selective, covalent prostaglandin reductase 2 (PTGR2) inhibitor with IC50 of 100 nM (human PTGR2), covalently ligands the noncatalytic Y100 and Y265 residues located in the substrate binding pocket.

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    Biological Activity

    RJG-2036 is a potent, selective, covalent prostaglandin reductase 2 (PTGR2) inhibitor with IC50 of 100 nM (human PTGR2), covalently ligands the noncatalytic Y100 and Y265 residues located in the substrate binding pocket.
    RJG-2036 blocks recombinant PTGR2 biochemical activity with IC50 of 176 nM.
    RJG-2036 ligands the noncatalytic Y100 and Y265 sites on PTGR2.
    RJG-2036 (10 uM) suppresses LPS-stimulated TNF-α response in THP1 macrophages, alters the activity of PTGR2-regulated eicosanoids.

    Physicochemical Properties

    M.Wt 427.48
    Formula C20H21N5O4S
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20°C 12 Months; 4°C 6 Months
    In Solvent
    -80°C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    (3-((1H-1,2,4-triazol-1-yl)sulfonyl)phenyl)(4-(2-methoxyphenyl)piperazin-1-yl)methanone

    References

    1. Founds MW, et al. ACS Chem Biol. 2025 May 19. doi: 10.1021/acschembio.5c00231.

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