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NLRP3-IN-51(Compound 3q)作为一种高效的胆碱能抗炎通路(CAP)激活剂,显示了在THP-1细胞中抑制由尿酸钠(MSU)诱导的IL-1β产生,有助于抗痛风性关节炎。该化合物同样抑制了MSU诱导的NF-κBp65磷酸化,而对NLRP3、pro-caspase 1以及caspase-1的自我裂解与激活则无明显影响。据此,NLRP3-IN-51在CAP的激活下有效抑制NLRP3的活化初期。
NLRP3-IN-51(Compound 3q)作为一种高效的胆碱能抗炎通路(CAP)激活剂,显示了在THP-1细胞中抑制由尿酸钠(MSU)诱导的IL-1β产生,有助于抗痛风性关节炎。该化合物同样抑制了MSU诱导的NF-κBp65磷酸化,而对NLRP3、pro-caspase 1以及caspase-1的自我裂解与激活则无明显影响。据此,NLRP3-IN-51在CAP的激活下有效抑制NLRP3的活化初期。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | NLRP3-IN-51 (Compound 3q) is an effective activator of the cholinergic anti-inflammatory pathway (CAP). This compound demonstrates potential for treating gouty arthritis as it inhibits the production of IL-1β in THP-1 cells induced by monosodium urate (MSU). Furthermore, NLRP3-IN-51 suppresses the phosphorylation of NF-κBp65 triggered by MSU without impacting the self-cleavage and activation of NLRP3, pro-caspase 1, or the second messenger caspase-1. Therefore, the initial stage of NLRP3 inhibition by NLRP3-IN-51 occurs through the activation of CAP. |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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