Chemical Structure : Clonixeril
Catalog No.: PC-24871Not For Human Use, Lab Use Only.
Clonixeril (CXL) is a highly potent, non-nucleotide hSTING modulator, has two modes of interaction with hSTING, shows weak agonist activity at micromolar concentrations, acts as a hSTING antagonist at <1 nM (EC50 < 1fM).
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Clonixeril (CXL) is a highly potent, non-nucleotide hSTING modulator, has two modes of interaction with hSTING, shows weak agonist activity at micromolar concentrations, acts as a hSTING antagonist at <1 nM (EC50 < 1fM).
Clonixeril displays this exceptionally strong inhibitory effect on hSTING mediated IFN-1 production using a THP-1 cell luciferase reporter for interferon regulatory factor 3 (IRF3).
Clonixeril is a potent inhibitor of hSTING, with activity even at attomolar (10-18 M) concentrations
Clonixeril reduces hSTING oligomerization at concentrations down to attomolar levels with an inverse dose response.
Clonixeril binds to hSTING CTD with SPR KD of 430 nM.
M.Wt | 336.77 | |
Formula | C16H17ClN2O4 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Sparks RP, et al. ACS Cent Sci. 2025 Jun 6;11(6):994-1008.
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