Chemical Structure : DDO-7432
Catalog No.: PC-27714Not For Human Use, Lab Use Only.
DDO-7432 is a specific, orally bioavailable molecular glue that induces aberrant STING oligomerization, inhibits STING activity with IC50 of 1.37 uM in IRF luciferase reporter assays in THP-1-Dual cells, induces self-association of STING to inhibit STING-dependent signal transduction.
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DDO-7432 is a specific, orally bioavailable molecular glue that induces aberrant STING oligomerization, inhibits STING activity with IC50 of 1.37 uM in IRF luciferase reporter assays in THP-1-Dual cells, induces self-association of STING to inhibit STING-dependent signal transduction.
DDO-7432 suppresses the inflammatory response induced by HSV-1 infection in THP-1 cells.
DDO-7432 (60 mg/kg administered intragastrically) partially suppressed IFN-β secretion in serum and downregulated the expression of Mx1 and Cxcl10 in C57BL/6JSTING-Hu mice.
DDO-7432 (30 or 60 mg/kg, oral gavage) significantly reduced ISGs expression and attenuated inflammatory parameters in muscle tissue from C57BL/6JSTING-Hu myositis model.
| M.Wt | 434.15 | |
| Formula | C17H8Cl2F3NO5 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Zi-Wen Feng, et al. Signal Transduct Target Ther. 2026 Aug 4;11(1):308.

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