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产品名称 | GSK-3 ↓ ↑ | GSK-3α ↓ ↑ | GSK-3β ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AZD2858 |
+
GSK-3, IC50: 68 nM |
99% | |||||||||||||||||
Bikinin | ✔ | 99%+ | |||||||||||||||||
GSK 3 Inhibitor IX |
++++
GSK-3, IC50: 5 nM |
99%+ | |||||||||||||||||
AZD1080 |
+++
GSK-3α, IC50: 6.9 nM |
++
GSK-3β, IC50: 31 nM |
99%+ | ||||||||||||||||
BIO-acetoxime |
+++
GSK-3α, IC50: 10 nM |
+++
GSK-3β, IC50: 10 nM |
95% | ||||||||||||||||
SB-216763 |
++
GSK-3α, IC50: 34.3 nM |
++
GSK-3β, IC50: ~34.3 nM |
98% | ||||||||||||||||
SB 415286 |
+
GSK-3α, IC50: 78 nM |
+
GSK-3β, IC50: ~78 nM |
99%+ | ||||||||||||||||
CHIR-98014 |
++++
GSK-3α, IC50: 0.65 nM |
++++
GSK-3β, IC50: 0.58 nM |
98% | ||||||||||||||||
LY2090314 |
++++
GSK-3α, IC50: 1.5 nM |
++++
GSK-3β, IC50: 0.9 nM |
99%+ | ||||||||||||||||
CHIR 99021 |
+++
GSK-3α, IC50: 10 nM |
++++
GSK-3β, IC50: 6.7 nM |
99%+ | ||||||||||||||||
TDZD-8 |
+
GSK-3β, IC50: 2 μM |
99%+ | |||||||||||||||||
Indirubin |
+
GSK-3β, IC50: 0.6 μM |
98% | |||||||||||||||||
IM-12 |
++
GSK-3β, IC50: 53 nM |
98% | |||||||||||||||||
TWS119 |
++
GSK-3β, IC50: 30 nM |
99% | |||||||||||||||||
1-Azakenpaullone |
+++
GSK-3β, IC50: 18 nM |
99%+ | |||||||||||||||||
AR-A014418 |
++
GSK-3β, Ki: 38 nM |
99%+ | |||||||||||||||||
Tideglusib |
+
GSK-3β, IC50: 60 nM |
98% | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
靶点 |
|
描述 | Glycogen synthase kinase 3β (GSK-3β), a component of the adenomatous polyposis coli/axin/GSK-3β complex, is involved in the ubiquitination and proteasomal degradation of β-catenin, which is the key molecule of the Wnt/β-catenin pathway [3]. Wnt/β-catenin pathway plays a critical role in carcinogenesis, embryonic development, i and insulin sensitivity[4]. TWS119 is a specific inhibitor of GSK-3β, its tight binding to GSK-3 was quantified by SPR and further demonstrated by its potent GSK-3 kinase inhibitory activity (IC50=30 nM) [5]. In vitro study revealed that treatment with TWS119 at dose 10 μM for 24 h of incubation not only significantly attenuated mRNA level of CD16 and increased the mRNA expression of CD206, but also reduced the percentage of CD16/32 positive cells and increased the percentage of CD206 positive cells in microglia cells stimulated by LPS plus IFN-γ, indicating a direct modulating effect of TWS119 on switch of microglial polarization from pro-inflammatory phenotype to antiinflammatory phenotype[6]. Another in vitro finding showed that TWS119 at dose of 7μM enhanced IL-2 production in Tcm cells from TILs, increased IL-2-secreting CD4+ Tem cells in TILs, and promoted the proliferation of CD8+ Teff cells in TILs from human lung cancer[7]. Furthermore, TWS119 had the ability to inhibit the activities of PC-3 cells and SW620 cells, suggesting its anticancer effect on prostate and colon cancer cells [8]. In an HCT116 xenograft tumor model, the tumor growth in BALB/c nude mice which received intratumoural injection with γδT cells pretreated with 2.0 μM of TWS119 was slower than the other groups, indicating its potent antitumor efficacy in vivo[9]. TWS119 ameliorated microglia-mediated neuroinflammatory status following ischemic stroke and promoted angiogenesis by modulating microglia to anti-inflammatory phenotype[6]. |
作用机制 | TWS119 binds to GSK-3β then activates the canonical Wnt-β catenin signaling pathway to result in β catenin accumulation, which leads to the expression of genes downstream of canonical Wnt signaling[10]. |
细胞系 | 浓度 | 检测类型 | 检测时间 | 活动说明 | 数据源 |
RAW 264.7 | 0-10000ng/ml | Cytotoxicity Assay | 24 h | induces cell death in a dose dependent manner | 24330853 |
Dose | Rat: 30 mg/kg[3] (i.p.) Mice: 20 mg/kg, 40 mg/kg[3](i.p.) |
Administration | i.p. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.14mL 0.63mL 0.31mL |
15.71mL 3.14mL 1.57mL |
31.41mL 6.28mL 3.14mL |
CAS号 | 601514-19-6 |
分子式 | C18H14N4O2 |
分子量 | 318.329 |
别名 | |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Keep in dark place,Sealed in dry,2-8°C |
溶解度 |
DMSO: 50 mg/mL(157.07 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |
IP 2% DMSO+2% Tween80+30% PEG300+water 2.4 mg/mL clear PO 0.5% CMC-Na 32 mg/mL suspension |