CCT020312

CCT020312

中文名称CCT020312
中文同义词化合物 T14902;化合物CCT020312;6-溴-3-(5-(4-溴苯基)-1-(3-(二乙氨基)丙酰基)-4,5-二氢-1H-吡唑-3-基)-4-苯基喹啉-2(1H)-酮
英文名称CCT020312
英文同义词2(1H)-Quinolinone, 6-bromo-3-[5-(4-bromophenyl)-1-[3-(diethylamino)-1-oxopropyl]-4,5-dihydro-1H-pyrazol-3-yl]-4-phenyl-;CCT020312;CCT-020312,CCT020312
CAS号324759-76-4
分子式C31H30Br2N4O2
分子量650.4
EINECS号
相关类别
Mol文件324759-76-4.mol
结构式CCT020312 结构式

CCT020312 性质

密度1.48±0.1 g/cm3(Predicted)
储存条件Store at -20°C
溶解度可溶于DMSO
形态固体
酸度系数(pKa)9.43±0.70(Predicted)
颜色浅黄至黄色

CCT020312 用途与合成方法

CCT020312 是选择性的 EIF2AK3/PERK 的激活剂。CCT020312 可诱导细胞细胞中 EIF2A 的磷酸化。

EIF2AK3/PERK.

Treatment of HT29 cells with CCT020312 for 24 hours reveals a concentration-dependent loss of P-S608-pRB signal, with a linear response between 1.8 and 6.1 μM.
CCT020312 treatment effectively inhibits cell proliferation (as measured at 96 hours) even if treatment is for 2 hours only with subsequent compound washout, indicating that CCT020312 is capable of eliciting durable rather than transient cytostasis.
Treatment of HT29 cells with 10 μM CCT020312 for 24 hours reduces the amount of the G1/S cyclins D1, D2, E and A as well as the CDK catalytic subunit CDK2 and increased the level of the CDK inhibitor p27KIP1 present in such cells.

Treatment of 15-week-old wildtype mice with the PERK activator CCT020312 (1-5 mg/kg; i.p.; once daily for 3 days) leads to increased levels of phosphorylated PERK and NRF2 in brain homogenates.
P301S transgenic mice treated with CCT020312 (2 mg/kg; i.p.; once daily for 6 weeks) performes significantly better in Morris water maze.

Animal Model: 9-week-old P301S tau transgenic mice
Dosage: 2 mg/kg
Administration: Intraperitoneal injection; once daily for 6 weeks
Result: P301S transgenic mice treated with CCT020312 performed significantly better in Morris water maze.

安全信息

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/08/19HY-119240CCT0203121 mg818元
2024/08/19HY-119240CCT020312
CCT020312
324759-76-45mg1800元

CCT020312 上下游产品信息

"CCT020312"相关产品信息
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