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1010411-21-8

中文名称 GSK369796
英文名称 GSK369796
CAS 1010411-21-8
分子式 C20H24Cl3N3O
分子量 428.783
MOL 文件 1010411-21-8.mol
更新日期 2024/05/10 15:23:28
1010411-21-8 结构式 1010411-21-8 结构式

基本信息

中文别名
GSK369796二盐酸盐
化合物GSK369796 DIHYDROCHLORIDE
2-((叔丁基氨基)甲基)-5-((7-氯喹啉-4-基)氨基)苯酚 二盐酸盐
英文别名
CS-2373
GSK369796
GSK369796 HCL
GSK369796 2HCl
N-tert-butylisoquine
GSK 369796
GSK-369796
GSK369796 Dihydrochloride
GSK369796 (GSK-369796, GSK 369796)
5-[(7-Chloro-4-quinolinyl)amino]-2-[[(1,1-dimethylethyl)amino]methyl]phenol Hydrochloride
Phenol, 5-[(7-chloro-4-quinolinyl)amino]-2-[[(1,1-dimethylethyl)amino]methyl]-, hydrochloride
所属类别
生物化工:激动剂抑制剂

物理化学性质

储存条件Inert atmosphere,Room Temperature
溶解度DMSO:100.0(Max Conc. mg/mL);233.22(Max Conc. mM)
Water:50.0(Max Conc. mg/mL);116.61(Max Conc. mM)
形态固体

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H315-H319-H335
GSK369796价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-12082AGSK369796
GSK369796 Dihydrochloride
1010411-21-82mg1100元
2024/04/30HY-12082AGSK369796
GSK369796 Dihydrochloride
1010411-21-810mM * 1mLin DMSO1509元
2024/04/30HY-12082AGSK369796
GSK369796 Dihydrochloride
1010411-21-85mg1600元

常见问题列表

生物活性
GSK369796 Dihydrochloride (N-tert-butylisoquine)是 hERG potassium ion channel 重极化的抑制剂,其IC50值为7.5 μM。GSK369796 Dihydrochloride 是一种经济实惠且有效的4-氨基喹啉抗疟药。
靶点
TargetValue
hERG
(Cell-free assay)
7.5 μM
体外研究

In vitro , GSK369796 Dihydrochloride can inhibit the growth of Plasmodium falciparum strains 3D7c, HB3c and K1d, with IC 50 s of 11.2±2.2, 12.6±5.3 and 13.2±3.2 nM, respectively. Protein binding is higher for GSK369796 Dihydrochloride (compound 4) compare to desethyl amodiaquine in the mouse (93 vs 74%) but similar in human (88 vs 86%). GSK369796 Dihydrochloride can also inhibit hERG potassium ion channel repolarization with an IC 50 of 7.5±0.8 μM.

体内研究

In vivo , GSK369796 Dihydrochloride can inhibit the growth of Plasmodium berghei ANKA with ED 50 and ED 90 of 2.8 and 4.7 mg/kg, respectively.

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