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PKR-IN-C16
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
PKR-IN-C16图片
CAS NO:608512-97-6
包装与价格:
包装价格(元)
10 mM * 1 mL in DMSO电议
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品介绍
PKR-IN-C16 (Compound C16) 是一种特异的双链 RNA 依赖蛋白激酶 (PKR) 抑制剂。PKR-IN-C16 具有良好的神经保护作用,可挽救急性脑损伤。
生物活性

PKR-IN-C16 (Compound C16) is a specificdouble-stranded RNA-dependent protein kinase(PKR) inhibitor. PKR-IN-C16 shows promising neuroprotective properties and can rescue acute brain lesions[1].

IC50& Target

PKR[1]

体外研究
(In Vitro)

PKR-IN-C16 (Compound C16) is able to unlock the translation blockade induced by PKR in primary neuronal cultures[1].
PKR-IN-C16 (0.1 or 0.3 μM; 24 h) shows protective effect against the neuronal cell death induced by endoplasmic reticulum stress in SH-SY5Y cells[1].
PKR-IN-C16 (1-1000 nM; 4 h) prevents not only PKR-phosphorylation but also the activation of caspase-3 induced by Amyloid β in SH-SY5Y cells[2].

Western Blot Analysis[2]

Cell Line:Human SH-SY5Y cells
Concentration:1, 10, 20, 200, 1000 nM
Incubation Time:4 h
Result:Markedly reduces the level of phosphorylated PKR in the cells exposed to 20 μM Amyloid β.
体内研究
(In Vivo)

PKR-IN-C16 (Compound C16) (60 or 600 μg/kg; i.p.; 3 times) prevents not only the PKR-induced neuronal loss but also the inflammatory response in theQuinolinic acid(QA) (HY-100807) induced acute excitotoxic rat model[1]

Animal Model:Normotensive male Wistar rats, excitotoxic neuroinflammatory model, inflammation was induced by unilateral striatal injection of quinolinic acid (QA)[1]
Dosage:60 or 600 μg/kg
Administration:Intraperitoneal injection; 24 h, 2 h before QA injection and 24 h post-QA injection
Result:Reduced expression of the active catalytic domain of the PKR, prevented increase of IL-1β levels on the contralateral side (97% inhibition) at 600 μg/kg. Decreased by 47% the neuronal loss and by 37% the number of positive cleaved caspase-3 neurons induced by QA injection at 600 μg/kg.
分子量

268.29

性状

Solid

Formula

C13H8N4OS

CAS 号

608512-97-6

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : 7.35 mg/mL(27.40 mM;ultrasonic and warming and heat to 60℃)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM3.7273 mL18.6365 mL37.2731 mL
5 mM0.7455 mL3.7273 mL7.4546 mL
10 mM0.3727 mL1.8637 mL3.7273 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。