![](../../files/images/goods/868359-05-1.png)
WAY-213613
CAS No. 868359-05-1
WAY-213613 ( —— )
产品货号. M24877 CAS No. 868359-05-1
WAY-213613 是一种有效的选择性 GLT-1/EAAT2 非底物再摄取抑制剂 (IC50: 85 nM EAAT2)。
纯度: >98% (HPLC)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
![](/themes/theme/en/images/pdf.png)
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1702 | 有现货 |
![]() ![]() |
10MG | ¥2567 | 有现货 |
![]() ![]() |
25MG | ¥4542 | 有现货 |
![]() ![]() |
50MG | ¥6827 | 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WAY-213613
-
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WAY-213613 是一种有效的选择性 GLT-1/EAAT2 非底物再摄取抑制剂 (IC50: 85 nM EAAT2)。
-
产品描述WAY-213613 is a potent and selective nonsubstrate reuptake inhibitor of GLT-1/EAAT2 (IC50: 85 nM EAAT2). It displays 59- and 44-fold selectivity over EAAT1 and EAAT3 (IC50s: 5 and 3.8 μM, respectively). WAY-213613 shows no activity at ionotropic and metabotropic glutamate receptors.
-
体外实验WAY-213613 (0-100 μM) has inhibitory activity for human EAAT1, EAAT2 and EAAT3 subtype with IC50 values of 5004 nM, 85 nM and 3787 nM, respectively.WAY-213613 (3, 30, 300 nM) has the inhibitory effect on synaptosomal L-[3H] glutamate uptake with Ki values of 15 nM, 41 nM and 55 nM in the presence of 3, 30 and 300 nM, respectively.WAY-213613 (0-100 μM) produces a concentration-dependent block of glutamate-induced currents in EAAT1-, EAAT2- or EAAT3-injected oocytes, with IC50 values of 48, 0.13 and 4.0 μM, respectively.WAY-213613 (0.5–50 μM) exhibits good selectivity over ionotropic receptors and EAAT2 and potent activity toward blocking NMDA-stimulated responses.
-
体内实验——
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体EAAT2|EAAT3|EAAT1
-
研究领域——
-
适应症——
化学信息
-
CAS Number868359-05-1
-
分子量415.19
-
分子式C16H13BrF2N2O4
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESN[C@@H](CC(Nc(cc1)ccc1Oc(cc(c(F)c1)F)c1Br)=O)C(O)=O
-
化学全称——
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.Dunlop J, et al. Characterization of novel aryl-ether, biaryl, and fluorene aspartic acid and diaminopropionic acid analogs as potent inhibitors of the high-affinity glutamate transporter EAAT2. Mol Pharmacol. 2005 Oct;68(4):974-82. Epub 2005 Jul 13.
产品手册
![](/themes/theme/en/images/ct.png)
![](/themes/theme/en/images/new12.jpg)
![](/themes/theme/en/images/gift.jpg)
![](/themes/theme/en/images/ct2.png)
关联产品
-
E3 Ligase Ligand-Lin...
E3 Ligase Ligand-Linker Conjugates 2 是一种合成的 E3 连接酶配体-连接子缀合物,结合了基于 Pomalidomide 的 cereblon 配体和 4 单元 PEG 连接子。
-
NRX-252262
NRX-252262 是 β-连环蛋白及其同源 E3 连接酶 SCFβ-TrCP 之间相互作用的有效增强剂,可诱导突变型 β-连环蛋白降解 (EC50:3.8 nM)
-
1-Methyl-6,8-dimetho...
The root barks of Dictamnus dasycarpus.