Chemical Structure : CC-401 hydrochloride
CAS No.: 1438391-30-0
货号: PC-43332Not For Human Use, Lab Use Only.
CC-401 hydrochloride is a potent, selective, ATP-competitive pan-JNK inhibitor with Ki of 25-50 nM, displays >40-fold selectivity over other related kinases, including p38, ERK, IKK2, PK C, Lck, and ZAP70.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | ¥1580 | In stock | |
25 mg | ¥2580 | In stock | |
50 mg | ¥3780 | In stock | |
100 mg | Get quote |
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CC-401 hydrochloride is a potent, selective, ATP-competitive pan-JNK inhibitor with Ki of 25-50 nM, displays >40-fold selectivity over other related kinases, including p38, ERK, IKK2, PK C, Lck, and ZAP70.
CC-401 decreases hepatic necrosis and apoptosis after orthotopic liver transplantation in vivo.
CC-401 blocks JNK signaling in the rat obstructed kidney and significantly inhibits renal fibrosis in terms of interstitial myofibroblast accumulation and collagen IV deposition.
CC-401 also significantly reduces tubular apoptosis in the obstructed kidney.
CC-401 sensitizes hypoxic colon cancer cells to DNA-damaging agents, potentiates the effect of bevacizumab and oxaliplatin in HT29-derived mouse xenografts.
分子量 | 424.9265 | |
分子式 | C22H25ClN6O | |
外观性状 | Solid | |
储存条件 |
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Solubility |
100 mM in DMSO (42.4 mg/mL) |
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Chemical Name/SMILES |
1H-Indazole, 3-[3-[2-(1-piperidinyl)ethoxy]phenyl]-5-(1H-1,2,4-triazol-5-yl)-, hydrochloride (1:1) |
1. Uehara T, et al. Transplantation. 2004 Aug 15;78(3):324-32.
2. Uehara T, et al. J Hepatol. 2005 Jun;42(6):850-9.
3. Ma FY, et al. J Am Soc Nephrol. 2007 Feb;18(2):472-84.
4. Vasilevskaya IA, et al. Clin Cancer Res. 2015 Sep 15;21(18):4143-52.
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