Chemical Structure : cGAS inhibitor 36
货号: PC-23640Not For Human Use, Lab Use Only.
cGAS inhibitor 36 is a potent, orally bioavailable inhibitor of cyclic GMP-AMP synthase (cGAS) with biochemical IC50 of 32 nM and 5.8 nM for h-cGAS and m-cGAS respectively.
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cGAS inhibitor 36 is a potent, orally bioavailable inhibitor of cyclic GMP-AMP synthase (cGAS) with biochemical IC50 of 32 nM and 5.8 nM for h-cGAS and m-cGAS respectively.
cGAS inhibitor 36 shows cellular activity with a THP1 cGAMP cell assay with IC50 of 60 nM.
cGAS inhibitor 36 displayed a dose-dependent reduction in cGAMP production in a ConA pharmacodynamic mouse model of acute liver injury.
分子量 | 421.28 | |
分子式 | C19H18Cl2N4O3 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. Cyr P, et al. ACS Med Chem Lett. 2024 Nov 25;15(12):2201-2209.
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