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网站主页 >> CAS数据库列表 >> 3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐

3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐

生物活性 靶点 体外研究 体内研究 3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐 试剂级价格
3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐, 1438391-30-0, 结构式
3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐
CAS号:
1438391-30-0
英文名:
CC401 HCl
英文别名:
CC-401 (hydrochloride);CC-401 dihydrochloride >=95% (HPLC);CC 401 HYDROCHLORIDE; CC401 HYDROCHLORIDE; CC401 HCL;CC401 Hydrochloride,CC-401,Inhibitor,JNK,CC 401 Hydrochloride,CC 401,CC401,inhibit;3-(3-(2-(Piperidin-1-yl)ethoxy)phenyl)-5-(1H-1,2,4-triazol-5-yl)-1H-indazole hydrochloride;3-(3-(2-(piperidin-1-yl)ethoxy)phenyl)-5-(1H-1,2,4-triazol-3-yl)-1H-indazole hydrochloride;3-[3-[2-(1-Piperidinyl)ethoxy]phenyl]-5-(1H-1,2,4-triazol-5-yl)-1H-indazole hydrochloride (1:1)
中文名:
3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐
中文别名:
CC-401盐酸盐;化合物CC-401 HYDROCHLORIDE;JNK抑制剂(CC-401 HYDROCHLORIDE);3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐;3-(3-(2-(哌啶-1-基)乙氧基)苯基)-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐
CBNumber:
CB82666606
分子式:
C22H25ClN6O
分子量:
424.9265
MOL File:
1438391-30-0.mol

3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐化学性质

储存条件:
Store at -20°C
溶解度:
DMSO : 100 mg/mL (235.33 mM; Need ultrasonic)
形态:
White powder.
安全信息
海关编码: 2933399990

3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐性质、用途与生产工艺

生物活性

CC-401是有效的JNK抑制剂，其对JNK的选择性是对其他相关性激酶的选择性的至少40倍。

靶点

JNK

25-50 nM (Ki)

体外研究

CC-401 has at least 40-fold selectivity for JNK compared with other related kinases, including p38, extracellular signal-regulated kinase (ERK), inhibitor of κB kinase (IKK2), protein kinase C, Lck, zeta-associated protein of 70 kDa (ZAP70). In cell-based assays, 1 to 5 μM CC-401 provides specific JNK inhibition. CC-401, a small molecule that is a specific inhibitor of all three JNK isoforms. CC-401 competitively binds the ATP binding site in JNK, resulting in inhibition of the phosphorylation of the N-terminal activation domain of the transcription factor c-Jun. The specificity of this inhibitor is tested in vitro using osmotic stress of the HK-2 human tubular epithelial cell line. CC-401 inhibits sorbitol-induced phosphorylation of c-Jun in a dosage-dependent manner. However, CC-401 does not prevent sorbitol-induced phosphorylation of JNK, p38, or ERK.

体内研究

The staining of p-JNK is moderately induced in bevazicumab and Oxaliplatin treatments as compared to control, and in the CC-401-treated samples p-cJun content is significantly lower, consistent with effective JNK inhibition. DNA damage is modestly elevated in combined treatments with CC-401. CC-401 treatment from days 7 to 24 slows the progression of proteinuria, which is significantly reduced compared to the no-treatment and vehicle groups at days 14 and 21. However, there is still an increase in the degree of proteinuria at day 21 in CC-401-treated rats compared to proteinuria at day 5. The vehicle and no-treatment groups developed renal impairment at day 24 as shown by an increase in serum creatinine. This is prevented by CC-401 treatment.

3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐 上下游产品信息

上游原料

下游产品

3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐 试剂级价格

更新日期产品编号产品名称CAS编号包装价格
2024/04/30S67303-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐
CC-401 Hydrochloride		1438391-30-02mg794.8元
2024/04/30HY-130223-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐
CC-401 hydrochloride		1438391-30-010mM * 1mLin DMSO990元

3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐 生产厂家

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1438391-30-0, 3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐 相关搜索:

乙酰氯 3-甲基-3-哌啶醇 Binimetinib(MEK162) BKM-120 替沃扎尼 利索茶碱 卡博替尼 达克替尼 1,3-二氢-1-[1-[[4-(6-苯基-1H-咪唑并[4,5-G]喹喔啉-7-基)苯基]甲基]-4-哌啶基]-2H-苯并咪唑-2-酮 维罗非尼
  • API
  • 药靶配体
  • 细胞生物学试剂
  • C22H24N6OHCl
  • 3-(3-(2-(哌啶-1-基)乙氧基)苯基)-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐
  • 化合物CC-401 HYDROCHLORIDE
  • CC-401盐酸盐
  • JNK抑制剂(CC-401 HYDROCHLORIDE)
  • 3-[3-[2-(1-哌啶基)乙氧基]苯基]-5-(1H-1,2,4-三唑-5-基)-1H-吲唑盐酸盐
  • 1438391-30-0
  • 3-(3-(2-(Piperidin-1-yl)ethoxy)phenyl)-5-(1H-1,2,4-triazol-5-yl)-1H-indazole hydrochloride
  • CC401 Hydrochloride,CC-401,Inhibitor,JNK,CC 401 Hydrochloride,CC 401,CC401,inhibit
  • 3-(3-(2-(piperidin-1-yl)ethoxy)phenyl)-5-(1H-1,2,4-triazol-3-yl)-1H-indazole hydrochloride
  • CC-401 dihydrochloride >=95% (HPLC)
  • CC 401 HYDROCHLORIDE; CC401 HYDROCHLORIDE; CC401 HCL
  • 3-[3-[2-(1-Piperidinyl)ethoxy]phenyl]-5-(1H-1,2,4-triazol-5-yl)-1H-indazole hydrochloride (1:1)
  • CC-401 (hydrochloride)
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