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14653-77-1

中文名稱 硫代乙基氨基乙基胺鹽酸鹽
英文名稱 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 2024/12/12 20:05:44
14653-77-1 結(jié)構(gòu)式 14653-77-1 結(jié)構(gòu)式

基本信息

中文別名
氨磷汀硫醇
硫代乙基氨基乙基胺鹽酸鹽
氨磷汀硫醇 USP標(biāo)準(zhǔn)品
2-[(3-氨基丙基)氨基]乙硫醇二鹽酸鹽
英文別名
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)
所屬類別
分析化學(xué):藥典標(biāo)準(zhǔn)品和雜質(zhì)標(biāo)準(zhǔn)品

物理化學(xué)性質(zhì)

熔點(diǎn)184-186°C
儲存條件-20°C
溶解度H2O:≥20mg/mL
形態(tài)粉末
顏色白色至灰白色
穩(wěn)定性吸濕性

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07
警示詞危險
危險性描述H302-H318
危險品標(biāo)志Xn
危險類別碼22-41
安全說明26-39-41
WGK Germany3
海關(guān)編碼2930909165
毒性mouse,LD50,intraperitoneal,400mg/kg (400mg/kg),European Journal of Medicinal Chemistry--Chimie Therapeutique. Vol. 24, Pg. 48, 1989.

常見問題列表

生物活性
WR-1065 dihydrochloride 可以保護(hù)正常組織免受某些癌癥藥物的毒性作用,并通過 JNK 依賴性信號通路激活 p53。
靶點(diǎn)

p53

體外研究

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.

體內(nèi)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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