
WEHI-345
CAS No. 1354825-58-3
WEHI-345 ( WEHI-345 | WEHI345 | WEHI 345 )
产品货号. M11450 CAS No. 1354825-58-3
一种有效的选择性 RIPK2 抑制剂,IC50/Kd 为 130/46 nM;对 RIPK1、RIPK4 和 RIPK5 表现出可忽略不计的活性 (>10 uM)。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥864 | 有现货 |
![]() ![]() |
5MG | ¥1058 | 有现货 |
![]() ![]() |
10MG | ¥1676 | 有现货 |
![]() ![]() |
25MG | ¥4092 | 有现货 |
![]() ![]() |
50MG | ¥5821 | 有现货 |
![]() ![]() |
100MG | 获取报价 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称WEHI-345
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述一种有效的选择性 RIPK2 抑制剂,IC50/Kd 为 130/46 nM;对 RIPK1、RIPK4 和 RIPK5 表现出可忽略不计的活性 (>10 uM)。
-
产品描述A potent and selective RIPK2 inhibitor with IC50/Kd of 130/46 nM; displays negligible activity (>10 uM) against RIPK1, RIPK4 and RIPK5; delays RIPK2 ubiquitylation and NF-κB activation downstream of NOD engagement; prevents cytokine production in vitro and in vivo and ameliorates experimental autoimmune encephalomyelitis in mice.
-
体外实验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. Western Blot Analysis Cell 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.
-
体内实验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. 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.
-
同义词WEHI-345 | WEHI345 | WEHI 345
-
通路Apoptosis
-
靶点RIP kinase
-
受体RIPK2
-
研究领域Cancer
-
适应症——
化学信息
-
CAS Number1354825-58-3
-
分子量401.4643
-
分子式C22H23N7O
-
纯度>98% (HPLC)
-
溶解度DMSO: ≥ 32 mg/mL
-
SMILESO=C(NCC(C)(N1N=C(C2=CC=C(C)C=C2)C3=C(N)N=CN=C31)C)C4=CC=NC=C4
-
化学全称4-Pyridinecarboxamide, N-[2-[4-amino-3-(4-methylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-2-methylpropyl]-
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Nachbur U, et al. Nat Commun. 2015 Mar 17;6:6442.
产品手册




关联产品
-
GSK547
GSK547 (RIP1i, GSK 547) 是一种高度选择性且有效的 RIP1 激酶抑制剂,可在体内强力靶向 RIP1。
-
RIPK2-IN-2
一种有效的选择性受体相互作用蛋白 2 (RIP2) 激酶抑制剂。
-
RIP2 Kinase Inhibito...
RIP2 Kinase Inhibitor 3 是一种高效、选择性的受体相互作用蛋白 -2 (RIP2) 激酶抑制剂,IC50 值为 1 nM。