Chemical Structure : S-570
Catalog No.: PC-27724Not For Human Use, Lab Use Only.
S-570 is a potent, covalent, orally available STING antagonist with IC50 of 41 nM (hSTING), covalently binds to Cys91, inhibits IFN-β secretion in 2′,3′-cGAMP-stimulated THP-1 cells with IC50 of 18 nM.
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S-570 is a potent, covalent, orally available STING antagonist with IC50 of 41 nM (hSTING), covalently binds to Cys91, inhibits IFN-β secretion in 2′,3′-cGAMP-stimulated THP-1 cells with IC50 of 18 nM.
S-570 selectively inhibits STING signaling while showing only minimal activity against RIG-I- or TLR4-mediated innate immune signaling pathways.
S-570 also exhibits potent antagonist activity against mouse STING with IC50 of 71 nM in cell-based reporter assay using B16 cells stimulated with the STING agonist CMA (10-carboxymethyl-9-acridanone).
S-570 significantly suppressed plasma levels of IFN-β, IL-6 and TNF-α stimulated by CMA in mice.
S-570 effectively attenuated systemic inflammation in a CMA-stimulated mouse model.
| M.Wt | 364.76 | |
| Formula | C17H12ClF3N4 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Kiyoi T, et al. Bioorg Med Chem Lett. 2026 Aug 6;141:130757.

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