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NSC 102533

目录号: A22680

P2X7 receptor 拮抗剂

NSC 102533 是一种高效的嘌呤能 P2X7 受体拮抗剂,该受体是一种参与炎症与免疫调控的配体门控离子通道。NSC 102533 能有效抑制在表达人体 P2X7 受体的 HEK293 细胞中由 ATP 诱导的染料摄取,其半数抑制浓度(IC₅₀)为 22.4 nM。它还可抑制人 THP-1 单核细胞和小鼠腹腔巨噬细胞中由 ATP 诱导的 IL-1β 分泌,IC₅₀ 分别为 9.8 nM 和 11.2 nM,显示出显著的抗炎活性。

除了免疫调节作用外,NSC 102533 还表现出抗蛇毒潜能,可浓度依赖性地抑制蝮蛇属(Bothrops atrox)毒液的蛋白水解活性。在体内实验中,皮下注射 NSC 102533(3 mg/kg)可显著减少由 B. atrox 和 B. jararaca 毒液诱导的皮肤出血,并在 0.01–1 mg/kg 剂量范围内减轻小鼠角叉菜胶诱导的足肿胀。上述特性表明,NSC 102533 是研究 P2X7 受体介导的炎症反应及蛇毒相关病理过程的宝贵药理学工具化合物。

 
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1mg
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5mg
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10mM * 1mL in DMSO
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生物活性
Discription

NSC 102533 is a potent antagonist of the purinergic P2X7 receptor, a ligand-gated ion channel involved in inflammation and immune regulation. It effectively inhibits ATP-induced dye uptake in HEK293 cells expressing human P2X7 receptors with an IC₅₀ of 22.4 nM. NSC 102533 also suppresses ATP-induced IL-1β secretion in human THP-1 monocytes and primary mouse peritoneal macrophages, with IC₅₀ values of 9.8 nM and 11.2 nM, respectively, demonstrating strong anti-inflammatory activity.

In addition to its immunomodulatory effects, NSC 102533 exhibits antivenom potential by inhibiting Bothrops atrox venom proteolysis in a concentration-dependent manner. In in vivo studies, intradermal administration of NSC 102533 (3 mg/kg) significantly reduces skin hemorrhage induced by B. atrox and B. jararaca venom and attenuates carrageenan-induced paw edema in mice at doses between 0.01 and 1 mg/kg. These properties highlight NSC 102533 as a valuable pharmacological tool for studying P2X7 receptor–mediated inflammatory responses and venom-induced pathology.

 
产品信息
目录号 A22680
分子式 C16H10O3
分子量 250.25
CAS号 1150-59-0
SMILES C1=CC=C(C=C1)C2=C(C3=CC=CC=C3C(=O)C2=O)O
其他名称 NSC102533,NSC-102533
储存条件

Store lyophilized at -20ºC, keep desiccated.
In lyophilized form, the chemical is stable for 36 months.
In solution, store at -20ºC and use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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