您好,欢迎来到试剂信息网! [登录] [免费注册]
试剂信息网
位置:首页 > 产品库 > Zunsemetinib
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
Zunsemetinib
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。
Zunsemetinib图片
CAS NO:1640282-42-3
包装与价格:
包装价格(元)
5mg电议
10mg电议
50mg电议
100mg电议

产品名称
ATI-450
CDD-450
产品介绍
Zunsemetinib (CDD-450) 是一种具有口服活性的 p38α 丝裂原激活蛋白激酶激活蛋白激酶2 (MK2)通路抑制剂。Zunsemetinib 可用于免疫炎症性疾病的研究。
生物活性

Zunsemetinib (CDD-450) is an orally active and selectivep38αmitogen-activated protein kinase-activated protein kinase 2 (MK2) pathway inhibitor. Zunsemetinib can be used for the research of immuno-inflammatory diseases[1].

IC50& Target

MK2[1]

体外研究
(In Vitro)

Zunsemetinib (1 and 10 μM; 1 hour; WT and NOM ID BMMs) has no effect on NLRP3 expression, but decreases IL-1β expression by promoting IL-1β mRNA degradation[1].
Zunsemetinib (0.4 nM~1 μM; 16 hours; PBMC) reduces IL-1β secretion and promotes IL-1β mRNA instability[1].
Zunsemetinib selectively blocks p38α MAPK activation of the proinflammatory kinase MK2 while sparing p38α activation of other effectors such as PRAK and ATF2. Zunsemetinib inhibits in vitro osteoclast formation induced by RANKL[1].

RT-PCR[1]

Cell Line:WT and NOM ID BMMs
Concentration:1 and 10 μM
Incubation Time:1 hour
Result:Had no effect on NLRP3 expression, but decreased IL-1β expression by promoting IL-1β mRNA degradation.
体内研究
(In Vivo)

Zunsemetinib (1,000 ppm; p.o.) blocks LPS-induced TNF-α expression persisted for up to 4 weeks after dosing[1].
Zunsemetinib (10 and 20 mg/kg; p.o.) increases bone density[1].
Zunsemetinib prevents osteopenia in NOM IDcmice through inhibition of osteoclastogenesis[1].

Animal Model:8-week-old WT female mice[1]
Dosage:1,000 ppm
Administration:P.o.
Result:Blocked LPS-induced TNF-α expression persisted for up to 4 weeks after dosing.
Animal Model:Rats[1]
Dosage:10 and 20 mg/kg
Administration:P.o.
Result:Increased bone density.
Clinical Trial
分子量

513.92

性状

Solid

Formula

C25H22ClF2N5O3

CAS 号

1640282-42-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : 100 mg/mL(194.58 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.9458 mL9.7291 mL19.4583 mL
5 mM0.3892 mL1.9458 mL3.8917 mL
10 mM0.1946 mL0.9729 mL1.9458 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。