WAY-213613 hydrochloride
目录号: PL01622 纯度: ≥99%
商品编号 规格 价格 会员价 是否有货 数量
PL01622-5mg 5mg ¥1978.18 请登录
PL01622-10mg 10mg ¥2596.36 请登录
PL01622-25mg 25mg ¥5934.55 请登录
PL01622-50mg 50mg ¥9890.91 请登录
PL01622-100mg 100mg ¥17309.09 请登录
PL01622-200mg 200mg 询价 询价
PL01622-500mg 500mg 询价 询价
PL01622-10mM*1mLinDMSO 10mM*1mLinDMSO ¥2176.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
WAY-213613 hydrochloride
英文名称
WAY-213613 hydrochloride
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
WAY-213613 (hydrochloride) 是一种有效的选择性人 EAAT2 抑制剂。WAY-213613 具有有效的 EAAT2 抑制活性,IC50 值为 85 nM。WAY-213613 可用于中枢神经系统的研究。
生物活性
WAY-213613 (hydrochloride) is a potent and selective human EAAT2 inhibitor. WAY-213613 has potent EAAT2 inhibitory activity with an IC 50 value of 85 nM. WAY-213613 can be used for the research of central nervous system.
性状
Solid
IC50 & Target[1][2]
IC50: 5004 nM (EAAT1); 85 nM (EAAT2); 3787 nM (EAAT3)
体外研究(In Vitro)
WAY-213613 (hydrochloride) (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-[H] 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- orEAAT3-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. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
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.
[2]. Simmons DA, et al. A small molecule p75NTR ligand, LM11A-31, reverses cholinergic neurite dystrophy in Alzheimers disease mouse models with mid- to late-stage disease progression. PLoS One. 2014 Aug 25;9(8):e102136.
溶解度数据
In Vitro: DMSO : 50 mg/mL (110.71 mM; warming and heat to 80°C)H2O : < 0.1 mg/mL (insoluble)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2