Calpain Inhibitor XII
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 1mg | ¥2964.00 | 10-15工作日发货 | |
| 5mg | ¥7410.00 | 10-15工作日发货 | |
| 10mg | ¥11856.00 | 10-15工作日发货 |
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
Ki: 19 nM for μ-calpain
Calpain Inhibitor XII is a reversible and selective inhibitor of calpain I.
Calpain is a protein belonging to the family of calcium-dependent, non-lysosomal cysteine proteases expressed ubiquitously in mammals and many other organisms. Calpain inhibitors have been used to study the role of calpains in diverse processes, including neutrophil chemotaxis, neuronal signaling, and cardiac response to injury.
In vitro: A series of new dipeptidyl alpha-keto amides of the general structure R1-L-Leu-D,L-AA-CONH-R2 including Calpain Inhibitor XII were synthesized and evaluated as inhibitors for the cysteine proteases calpain I, calpain II, and cathepsin B. Calpain II was more sensitive to these inhibitors Calpain Inhibitor XII than calpain I. Calpain I was also effectively inhibited by Calpain Inhibitor XII, but lower Ki values than with calpain II. Cathepsin B was weakly inhibited by Calpain Inhibitor XII. The best calpain I inhibitor in this study was Calpain Inhibitor XII with Ki value of 19 nM [1].
In vivo: Up to now, there is no animal in vivo data reported.
Clinical trial: So far, no clinical study has been conducted.
Reference:
[1] Li, Z. ,Ortega-Vilain, A.C.,Patil, G.S., et al. Novel peptidyl α-keto amide inhibitors of calpains and other cysteine proteases. Journal of Medicinal Chemistry 39(20), 4089-4098 (1996).
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 181769-57-3 |
| 分子式 | C26H34N4O5 |
| 分子量 | 482.6 |
| 小分子别名 | (Rac)-Calpain Inhibitor XII |
| 化学名称 | [3-methyl-1-[[[1-[oxo[(2-pyridinylmethyl)amino]acetyl]butyl]amino]carbonyl]butyl]-carbamic acid, phenylmethyl ester |
| 溶解度 | ≤16mg/ml in ethanol;16mg/ml in DMSO;20mg/ml in dimethyl formamide |
| SMILES | CCCC(C(C(NCc1ncccc1)=O)=O)NC(C(CC(C)C)NC(OCc1ccccc1)=O)=O |
| 存储条件 | -20°C |
| 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 | (Rac)-钙蛋白酶抑制剂 XII 是钙蛋白酶 I(μ-钙蛋白酶,Ki=19 nM)的可逆选择性抑制剂。 (Rac)-钙蛋白酶抑制剂 XII 对钙蛋白酶 II(m-钙蛋白酶,Ki=120 nM)和 cathepsin B(Ki=750 nM)的亲和力较低。(Rac)-钙蛋白酶抑制剂 XII 有助于研究钙蛋白酶在中性粒细胞趋化、神经元信号传导和心脏损伤反应等多种过程中的作用。 |



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