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14653-77-1

中文名称 硫代乙基氨基乙基胺盐酸盐
英文名称 Amifostine Thiol Dihydrochloride
CAS 14653-77-1
分子式 C5H14N2S
分子量 134.243
MOL 文件 14653-77-1.mol
更新日期 2024/05/20 09:53:29
14653-77-1 结构式 14653-77-1 结构式

基本信息

中文别名
氨磷汀硫醇
硫代乙基氨基乙基胺盐酸盐
氨磷汀硫醇 USP标准品
2-[(3-氨基丙基)氨基]乙硫醇二盐酸盐
英文别名
WR-1065 2HCl
AMifostine Thiol
WR-1065 dihydrochloride
Amifostine Thiol Dihydrochloride
Amifostine Thiol Dihydrochloride (90%)
Amifostine Impurity 2(Amifostine Thiol)
2-[(3-AMinopropyl)aMino]ethanethiol Hydrochloride
2-[(3-Aminopropyl)amino]ethanethioldihydrochloride
2-[(3-aminopropyl)amino]ethane-1-thiol dihydrochloride
Amifostine Thiol (50 mg) (2-[(3-aminopropyl)amino]ethanethiol, dihydrochloride)
所属类别
分析化学:药典标准品和杂质标准品

物理化学性质

熔点184-186°C
储存条件-20°C
溶解度H2O:≥20mg/mL
形态粉末
颜色白色至灰白色
稳定性吸湿性

安全数据

危险性符号(GHS)
GHS05,GHS07
警示词危险
危险性描述H302-H318
危险品标志Xn
危险类别码22-41
安全说明26-39-41
WGK Germany3
海关编码2930909165
毒性mouse,LD50,intraperitoneal,400mg/kg (400mg/kg),European Journal of Medicinal Chemistry--Chimie Therapeutique. Vol. 24, Pg. 48, 1989.

常见问题列表

生物活性
WR-1065 dihydrochloride 可以保护正常组织免受某些癌症药物的毒性作用,并通过 JNK 依赖性信号通路激活 p53。
靶点

p53

体外研究

The DNA-binding activity is increased in a WR-1065 dihydrochloride (WR-1065) concentration-dependent manner. Cells treated with 1 mM WR-1065 dihydrochloride for 24 h reveal that all of the p53-induced genes analyzed are transactivated following WR-1065 dihydrochloride treatment, in a p53-dependent manner. Significantly, treatment with WR-1065 dihydrochloride leads to a 3-fold increase in luciferase expression driven by AP-1, and a 5-fold increase when this reporter gene is driven by NF-κB, when these values are normalized to the level of the cotransfected β-galactosidase gene.

体内研究

The results show that wR-1065 dihydrochloride (WR-1065) attenuates the severity of 6-OHDA-induced catalepsy (P<0.001) when compare with 6-OHDA-lesioned rats. Also it has been observed that WR-1065 dihydrochloride improves catalepsy in dose dependent manner (P<0.001). Pretreatment with three different doses of WR-1065 dihydrochloride (20, 40 and 80 μg/2 μL/rat) for 3 days before 6-OHDA administration, significantly (P<0.001) elevates SOD activity and restores it to normal range compare with 6-OHDA lesioned rats.

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