Chemical Structure : RJG-2036
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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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.
M.Wt | 427.48 | |
Formula | C20H21N5O4S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Founds MW, et al. ACS Chem Biol. 2025 May 19. doi: 10.1021/acschembio.5c00231.
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