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CC-401 HCl {[allProObj[0].p_purity_real_show]}

货号:A101734 同义名: CC-401 Hydrochloride

CC-401 HCl是一种选择性且ATP竞争性的JNK抑制剂,Ki值范围为25-50 nM。

CC-401 HCl 化学结构 CAS号:1438391-30-0
CC-401 HCl 化学结构
CAS号:1438391-30-0
CC-401 HCl 3D分子结构
CAS号:1438391-30-0
CC-401 HCl 化学结构 CAS号:1438391-30-0
CC-401 HCl 3D分子结构 CAS号:1438391-30-0
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CC-401 HCl 纯度/质量文件 产品仅供科研

货号:A101734 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 JNK JNK1 JNK2 JNK3 其他靶点 纯度
Mulberroside A 99%+
Loureirin B Calcium Channel,Potassium Channel 99%+
Ginsenoside Re NF-κB 98%
(+)-(3R,8S)-Falcarindiol STAT,ERK 99%+
trans-Zeatin p38 MAPK,ERK 95+%
Urolithin B ERK,NF-κB 95%
Cucurbitacin IIb NF-κB 99%
Astragaloside IV Akt,mTOR,NF-κB 98%
NDMC101 99%+
DB07268 ++++

JNK1, IC50: 9 nM

99%+
SP600125 +

MKK4, IC50: 0.4 μM

+++

JNK1, IC50: 40 nM

+++

JNK2, IC50: 40 nM

+++

JNK3, IC50: 90 nM

98%
JNK-IN-7 ++++

JNK1, IC50: 1.5 nM

++++

JNK2, IC50: 2 nM

++++

JNK3, IC50: 0.7 nM

99%
JNK-IN-8 ++++

JNK1, IC50: 4.7 nM

+++

JNK2, IC50: 18.7 nM

++++

JNK3, IC50: 1 nM

99%+
3,3',5-Triiodo-L-thyronine ++

JNK1, Kd: 240 nM

++

JNK2, Kd: 290 nM

+++

JNK3, Kd: 66 nM

98%
IQ-1S free acid +

JNK1, IC50: 390 nM

++

JNK2, IC50: 360 nM

+++

JNK3, IC50: 87 nM

99%
BI-78D3 ++

JNK, IC50: 280 nM

++

JNK, IC50: 280 nM

++

JNK, IC50: 280 nM

++

JNK, IC50: 280 nM

99%+
Bentamapimod +++

JNK1, IC50: 80 nM

+++

JNK2, IC50: 90 nM

++

JNK3, IC50: 230 nM

98%
Resveratrol +

JNK1, IC50: 50 μM

98%
Indirubin-3′-oxime 99%+
SU3327 +

JNK, IC50: 0.7 μM

+

JNK, IC50: 0.7 μM

+

JNK, IC50: 0.7 μM

+

JNK, IC50: 0.7 μM

99%+
JNK Inhibitor VIII ++++

JNK1, Ki: 2 nM

JNK1, IC50: 45 nM

++++

JNK2, IC50: 160 nM

JNK2, Ki: 4 nM

+++

JNK3, Ki: 52 nM

98%
Doramapimod 99%+
RPI-1 99%
TCS JNK 5a ++

JNK2, pIC50: 6.5

++

JNK3, pIC50: 6.7

98%
SP 600125, negative control +

JNK2, IC50: 18 μM

+

JNK3, IC50: 24 μM

97%
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。

CC-401 HCl 生物活性

描述 The c-Jun N-terminal kinase (JNK) signaling plays an important role in tubular cell apoptosis. CC-401 is a potent, small-molecule JNK inhibitor with Ki values of 25-50nM for three forms of JNK. It inhibits JNK in cell-based assays at a concentration of 1-5μM. CC-401 dose-dependently inhibited sorbitol-induced phosphorylation of c-Jun in HK-2 human tubular epithelial cell line at doses of 0.25-4μM. The oral administration of rats underwent unilateral ureteral obstruction with CC-401 (100mg/kg, twice daily) for 7 days reduced interstitial volume, the accumulation of α-SMA+ myofibroblasts, and collagen IV deposition as compared to the vehicle-treated group. Rats treated with CC-401 also showed reduced mRNA expressions of TGF-β1, connective tissue growth factor, and collagen IV in the kidney compared with vehicle-treated animals[3].
作用机制 CC-401 is a JNK inhibitor that competitively binds to the ATP binding site of JNK, inhibiting the phosphorylation of the N-terminal activation domain of c-Jun[3].

CC-401 HCl 参考文献

[1]Vasilevskaya IA, Selvakumaran M, et al. Inhibition of JNK Sensitizes Hypoxic Colon Cancer Cells to DNA-Damaging Agents. Clin Cancer Res. 2015 Sep 15;21(18):4143-52.

[2]Uehara T, Bennett B, et al. JNK mediates hepatic ischemia reperfusion injury.J Hepatol. 2005 Jun;42(6):850-9.

[3]Ma FY, Flanc RS, Tesch GH, et al. A pathogenic role for c-Jun amino-terminal kinase signaling in renal fibrosis and tubular cell apoptosis. J Am Soc Nephrol. 2007;18(2):472-484. doi:10.1681/ASN.2006060604

CC-401 HCl 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.35mL

0.47mL

0.24mL

11.77mL

2.35mL

1.18mL

23.53mL

4.71mL

2.35mL

CC-401 HCl 技术信息

CAS号1438391-30-0
分子式C22H25ClN6O
分子量 424.926
别名 CC-401 Hydrochloride
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Keep in dark place,Inert atmosphere,Room temperature

溶解度

DMSO: 105 mg/mL(247.1 mM),配合低频超声助溶,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

H2O: 12 mg/mL(28.24 mM),配合低频超声助溶

动物实验配方
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