Pyrrolidinedithiocarbamate ammonium
NF-κB抑制剂
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 1mL(10 mM in DMSO) | ¥454.00 | 现货 | |
| 50mg | ¥272.00 | 现货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
Pyrrolidinedithiocarbamate Ammonium is a potent inhibitor of nuclear factor-κB (NF-κB) [1].
NF-κB is a protein complex that controls DNA transcription and cytokine production. It is not only an important factor in regulating inflammation and immune responses and cell survival, but also involved in the cell transformation and tumor formation [1].
In human intestinal epithelial cell line HT-29 induced by interleukin-1β (IL-1β), pretreatment of cells with Pyrrolidinedithiocarbamate Ammonium (3 ~ 1000 μM) dose-dependently attenuated interleukin-8 (IL-8) production. Furthermore, Pyrrolidinedithiocarbamate Ammonium (100 μM) suppressed the accumulation of IL-8 mRNA. Pyrrolidinedithiocarbamate Ammonium inhibited the activation of NF-κB, by suppressing both NF-κB DNA binding and NF-κB-dependent transcriptional activity [2].
In Sprague-Dawley rats pretreated with bacillus Calmette-Guérin (BCG), injection of Pyrrolidinedithiocarbamate Ammonium (50, 100, and 200 mg/kg) reversed hepatic injury stimulated by BCG in vivo. Moreover, Pyrrolidinedithiocarbamate Ammonium inhibited down-regulation of Cytochrome P450 2E1 (CYP2E1) in a dose dependent manner, with ED50 value of 76 mg/kg [1].
References:
[1]. Qin J D, Cao Z H, Li X F, et al. Effect of ammonium pyrrolidine dithiocarbamate (PDTC) on NF-κB activation and CYP2E1 content of rats with immunological liver injury. Pharmaceutical Biology, 2014, 52(11): 1460-1466.
[2]. Németh Z H, Deitch E A, Szabó C, et al. Pyrrolidinedithiocarbamate inhibits NF-kappaB activation and IL-8 production in intestinal epithelial cells. Immunology Letters, 2003, 85(1): 41-46.
产品性质
| 物理外观 | A solid |
| CAS号 | 5108-96-3 |
| 分子式 | C5H12N2S2 |
| 分子量 | 164.28 |
| 化学名称 | ammonium pyrrolidine-1-carbodithioate |
| 溶解度 | insoluble in H2O; ≥12.975 mg/mL in EtOH with gentle warming; ≥7.3 mg/mL in DMSO |
| SMILES | [S-]C(N1CCCC1)=S.[NH4+] |
| 存储条件 | 室温 |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | 吡咯烷二硫代氨基甲酸铵是一种选择性 NF-κB 抑制剂;可抑制一氧化氮合酶 mRNA 的翻译;防止诱导。 |



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