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{[ getRatePrice(item.pr_rmb, 1,1) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,1) ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate) ]} | 现货 | 咨询 | - + |
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产品名称 | Cysteine Protease ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Z-FA-FMK | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Leupeptin hemisulfate | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
PMSF | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
PD 151746 |
+
μ-Calpain, IC50: 260 nM m-calpain, IC50: 5.33 μM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Odanacatib |
++++
Cathepsin K (human), IC50: 0.2 nM Cathepsin K (rabbit), IC50: 1 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
E-64 |
+++
Cysteine protease, IC50: 9 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
E 64c | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
E-64d | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
MG-101 | ✔ | {[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Calpeptin |
++
Calpain I (porcine erythrocytes), ID50: 52 nM Calpain II (porcine kidney), ID50: 40 nM |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
Cathepsin inhibitor 1 |
+++
Cathepsin L2, pIC50: 5.5 Cathepsin L, pIC50: 7.9 |
{[allProObj[0].p_purity_real_show]} | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | NSC 185058 functions as an inhibitor of ATG4B, a prominent cysteine protease. The use of NSC 185058 to inhibit ATG4B significantly reduces autophagic activity [1]. |
体内研究 | NSC185058 functions as an antagonist of ATG4B. ATG4B promotes autophagy by facilitating autophagosome formation via reversible modification of ATG8. The addition of the ATG4B inhibitor NSC185058 boosts the efficacy of radiation therapy (RT) against tumors. NSC185058 reduces the tumorigenicity of glioblastoma (GBM) cells and enhances the effectiveness of RT in orthotopic GBM xenograft models [1]. |
作用机制 | NSC185058 can bind to the pocket containing histidine 280 and aspartic acid 278, which are required for the proteolytic activity of ATG4B, through hydrophilic and hydrophobic binding interactions.[1] |
Dose | Mice: 150 mg/kg[2] (i.p.) |
Administration | i.p. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
4.65mL 0.93mL 0.46mL |
23.23mL 4.65mL 2.32mL |
46.45mL 9.29mL 4.65mL |
CAS号 | 39122-38-8 |
分子式 | C11H9N3S |
分子量 | 215.27 |
别名 | |
运输 | 蓝冰 |
存储条件 |
粉末 Keep in dark place,Inert atmosphere,Room temperature 液体 -20°C:3-6个月-80°C:12个月 |
溶解度 |
DMSO: 120 mg/mL(557.44 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |