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General description
A cell-permeable propenone compound that disrupts TNF receptor-associated factor 6 (TRAF6) and CD40 coupling by targeting TRAF6 via direct affinity interaction (Kd = 97 µM), effectively inhibiting LPS-induced NF-κB activation in murine macrophage RAW264.7 (IC50 15.9 µM; drug treatment starts 1 h prior to 2 h CD40 expression induction by LPS) as well as anti-CD40 antibody FGK45-stimulated IL-1β expression (IC50<10 µM; drug treatment starts 1 h prior to 6 h antibody stimulation). Daily intraperitoneal injection in vivo (10 µmol/kg/d = 2.513 mg/kg/d) during the last 6 weeks of a 12-week murine high fat diet-induce obesity (DIO) study is reported to improve insulin sensitivity, reduce hepatosteatosis, and prevent obesity-related inflammation in fat tissue (AT), as evidenced by a 40% less CD11b+F4/80+CD11c+ M1 macrophages in the stromal vascular fraction (SVF) of gonadal AT (gonAT) than the control DIO mice. Genetic studies likewise reveal that disruption of TRAF6-mediated CD40 signaling ameliorates obesity related complications, while CD40 knockout or deficit in TRAF2/3/5-CD40 interaction exacerbates metabolic complications in DIO mice.
A cell-permeable, bioavailable propenone compound that specifically targets TNF receptor-associated factor 6 (TRAF6; Kd = 97 µM for TRAF6 C-domain) and disrupts its functional coupling with CD40. A six-week treatment of C57BL/6 mice fed high fat diet (HFD) with this compound show significant improvement in insulin sensitivity and hepatosteatosis without affecting HFD-induced weight gain. Also reported to reduce gonadal adipose tissue inflammation and diminish the number of CD11b+F4/80+CD11c+ M1 macrophages. Inhibits NF-κB activation in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells (IC50 15.9 µM) and reduce IL-1β and IL-6 expression in anti-CD40 antibody FGK45-stimulated primary bone marrow-derived macrophages.
Biochem/physiol Actions
Cell permeable: yes
Primary Target
TRAF6
Packaging
Packaged under inert gas
Preparation Note
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Use only fresh DMSO for reconstitution.
Other Notes
Chatzigeorgiou, A., et al. 2014. Proc. Natl. Acad. Sci. USA111, 2686.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Standard Handling (A)
| assay | ≥95% (NMR) |
| Quality Segment | 100 |
| form | powder |
| manufacturer/tradename | Calbiochem® |
| storage condition | OK to freeze,protect from light |
| color | yellow |
| solubility | DMSO: 100 mg/mL |
| web metadata keyword.default | 3-((2,5-Dimethylphenyl)amino)-1-phenyl-2-propen-1-one CAS 433249-94-6,3-((2,5-Dimethylphenyl)amino)-1-phenyl-2-propen-1-one,CD40 antibody FGK45 stimulation inhibitor,CD40-TRAF6 Signaling Inhibitor 6877002,CD40-TRAF6 inhibitor 6877002,CD40-TRAF6 inhibitor IC50 15.9 µM,CD40-TRAF6 inhibitor for NF-kB research,CD40-TRAF6 signaling inhibitor,CD40-TRAF6 signaling pathway research reagent,Sigma-Aldrich CD40-TRAF6 inhibitor 6877002,high purity CD40-TRAF6 inhibitor for cell culture,immunology research CD40-TRAF6 inhibitor,lab-grade CD40-TRAF6 Signaling Inhibitor,propenone compound for macrophage studies |
| storage temp. | 2-8°C |
| SMILES string | COC(=O)C1=NC=NN1 |
| InChI | 1S/C4H5N3O2/c1-9-4(8)3-5-2-6-7-3/h2H,1H3,(H,5,6,7) |
| InChI key | QMPFMODFBNEYJH-UHFFFAOYSA-N |
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