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CAS No. : 2249435-90-1
MCE 国际站:SN-011
产品活性:SN-011 是一种有效和选择性的 STING 抑制剂,抑制 STING 信号传导的 IC50 值为 76 nM。SN-011 与环状二核苷酸 (CDN) 竞争 STING 二聚体的结合口袋,从而阻断 CDN 结合和 STING 激活。SN-011 可用于 STING 驱动的自身免疫和炎症性疾病的研究。
研究领域:Immunology/Inflammation
作用靶点:STING
In Vitro: SN-011 (1 μM; pretreated for 6 h) significantly suppresses the STING stimulator-induced expression of Ifnb, Cxcl10, and Il6 mRNA in mouse embryonic fibroblasts (MEFs).
SN-011 (0.001-10 μM; pretreated for 6 h) inhibits 2′3′-cGAMP-induced Ifnb expression in MEFs, mouse bone marrow-derived macrophages (BMDMs) and human foreskin fibroblasts (HFFs) with IC50s of 127.5, 107.1, and 502.8 nM, respectively.
SN-011 (1 μM; pretreated for 3 h) inhibits 2′3′-cGAMP-induced STING oligomerization and phosphorylation in HFFs.
SN-011 (1 μM) suppresses HSV-1 infection (4 h), HT-DNA (1 h), or 2′3′-cGAMP stimulation (30 min) induced STING ER-to-Golgi translocation.
In Vivo: SN-011 (5 mg/kg; i.p. 3 times weekly for a month) strongly inhibits hallmarks of inflammation and autoimmunity disease, and protects Trex1 / mice from death.
相关产品:Bioactive Compound Library Plus | Immunology/Inflammation Compound Library | Small Molecule Immuno-Oncology Compound Library | Highly Selective Inhibitors Library | Cyclic-di-GMP disodium | Dazostinag disodium | STING-IN-2 | CL845-PAB-Ala-Val-C5-MC | STING agonist-13 | STING agonist-26 | ADU-S100 ammonium salt | cGAMP | Ulevostinag | STING ligand-1 | STING agonist-28 | C-178 | C-176 | STING agonist-20 | 2',3'-cGAMP sodium | PROTAC STING Degrader-1 | CL656 | H-151 | STING agonist-12 | JAK-IN-23 | BSP16 | STING agonist-8 | STING modulator-5 | CCCP | IACS-8803 | STING agonist-11 | STING agonist-22 | STING agonist-24
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