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Product details
名称
WEHI-345
英文名称
WEHI-345
货号
W651350-5mg
包装规格
5mg
浓度
≥98%
储存温度
-20°C储存
运输条件
超低温冰袋运输
产品介绍
WEHI-345 is a potent and selective RIPK2 kinase inhibitor with an IC 50 of 0.13 μM, which delays RIPK2 ubiquitylation and NF-κB activation on oligomerization domain (NOD) stimulation In Vitro WEHI-345 (500 nM; Raw 267.4 cells) is able to inhibit MDP-induced autophosphorylation activity of RIPK2 in cells. WEHI-345 (500 nM; 0 hour, 2 hours, 4 hours, 8 hours; BMDMs or THP-1 cells) potently blocks MDP-induced transcription of the inflammatory mediators TNF and interleukin-6 (IL-6) in bone marrow-derived macrophages (BMDMs). In THP-1 cells, WEHI-345 reduces mRNA levels of NF-kB targets such as TNF, IL-8, IL-1b and A20. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: Raw 267.4 cells Concentration: 500 nM Incubation Time: Result: Inhibited MDP-induced autophosphorylation activity of RIPK2 in cells. RT-PCRCell Line: BMDMs or THP-1 cells Concentration: 500 nM Incubation Time: 0 hour, 2 hours, 4 hours, 8 hours Result: Blocked MDP-induced transcription of the inflammatory mediators TNF and interleukin-6 (IL-6) in BMDMs. And reduced mRNA levels of NF-kB targets in THP-1 cells. In Vivo WEHI-345 (20 mg/kg; intraperitoneal injection; twice daily; for 6 days; C57BL/6 male mice) treatment reduces disease score, inflammatory infiltrate, histological score and recruitment of dendritic cells to the site of inflammation. And improves body weight and reduces cytokine and chemokine levels, indicating an overall improvement of the condition in experimental autoimmune encephalomyelitis (EAE)-induced wild-type C57Bl/6 mice . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: C57BL/6 male mice (8-week-old) Dosage: 20 mg/kg Administration: Intraperitoneal injection; twice daily; for 6 days Result: Reduced disease score, inflammatory infiltrate, histological score and recruitment of dendritic cells to the site of inflammation. And improved body weight and reduced cytokine and chemokine levels. Form:Solid IC50& Target:IC 50 : 0.13 μM (RIPK2 kinase)
生化机理
WEHI-345 是一种强效的选择性 RIPK2 激酶抑制剂,IC50 为 0.13 μM,可延缓 RIPK2 泛素化和 NF-κB 在寡聚域(NOD)刺激下的激活。
CAS号
1354825-58-3
分子式
C22H23N7O
分子量
401.46 g/mol
PubChem编号
56602554
Isomeric SMILES
CC1=CC=C(C=C1)C2=NN(C3=NC=NC(=C23)N)C(C)(C)CNC(=O)C4=CC=NC=C4
IIUPAC Name
N-[2-[4-amino-3-(4-methylphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]-2-methylpropyl]pyridine-4-carboxamide
INCHI
1S/C22H23N7O/c1-14-4-6-15(7-5-14)18-17-19(23)26-13-27-20(17)29(28-18)22(2,3)12-25-21(30)16-8-10-24-11-9-16/h4-11,13H,12H2,1-3H3,(H,25,30)(H2,23,26,27)
InChi Key
LEBSTCDZKUSVOY-UHFFFAOYSA-N
Smiles
CC1=CC=C(C=C1)C2=NN(C3=NC=NC(=C23)N)C(C)(C)CNC(=O)C4=CC=NC=C4
PubChem CID
56602554
溶解性
DMSO : 25 mg/mL (62.27 mM; Need ultrasonic)
氢键供体数Hydrogen Bond Donor Count
2
氢键受体数Hydrogen Bond Acceptor Count
6
可旋转键计数Rotatable Bond Count
5
精确质量Exact Mass
401.196 Da
单同位素质量Monoisotopic Mass
401.196 Da
拓扑极表面积Topological Polar Surface Area
112.000 Ų
重原子数Heavy Atom Count
30
形式电荷Formal Charge
0
复杂度Complexity
586.000
同位素原子数Isotope Atom Count
0
共价键合单元计数Covalently-Bonded Unit Count
1
XLogP3
2.300
Safety
「No Dangerous Attributes」
Related
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WEHI-345 5mg

WEHI-345 5mg; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 5mg; ≥98%.

item number:W651350-5mg
Product model:5mg
level: 5mg; ≥98%
Lead Time:30days
sold 74 Items
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5mg

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