1. Metabolic Enzyme/Protease
  2. Phosphatase
  3. Z218484536

Z218484536 是一种选择性且可以透过血脑屏障的磷酸丝氨酸磷酸酶 (PSPH) 抑制剂。Z218484536 可以与 PSPH 结合,Kd 值约为 0.23 μM。Z218484536 降低星形胶质细胞中的 L-丝氨酸和 D-丝氨酸水平。Z218484536 能够抑制自发性癫痫发作,且不会引起严重副作用。Z218484536 在颞叶癫痫 (TLE) 模型中也显示了良好的抗癫痫效果。

MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

我们将采用定制合成服务的方式为您快速提供所需产品和技术服务

Z218484536 Chemical Structure

Z218484536 Chemical Structure

CAS No. : 1223877-07-3

1.  客户无需承担相应的运输费用。

2.  同一机构(单位)同一产品试用装仅限申领一次,同一机构(单位)一年内

     可免费申领三个不同产品的试用装。

3.  试用装只面向终端客户

规格 是否有货
50 mg   询价  
100 mg   询价  
250 mg   询价  

* Please select Quantity before adding items.

Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Z218484536 is a selective and brain-penetrant phosphoserine phosphatase (PSPH) inhibitor. Z218484536 binds to PSPH with a Kd value of approximately 0.23 μM. Z218484536 reduces L-serine and D-serine levels in astrocytes. Z218484536 is able to suppress spontaneous epileptic seizures without causing serious side effects. Z218484536 also shows good anti-epileptic effects in the temporal lobe epilepsy (TLE) model[1].

体外研究
(In Vitro)

Z218484536 (40-2,000 nM, 24 小时) 可抑制培养星形胶质细胞中 L-丝氨酸的释放,IC50为 0.4 μM,并降低细胞内 L-丝氨酸水平,IC50为 0.38 μM[1]

Z218484536 (0.078-40 μM, 48 小时) 对 HepG2 细胞增殖无毒性作用[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Z218484536 (0.5-20 mg/kg,腹腔注射,每日一次,3 天) 可延缓急性癫痫发作,降低癫痫发作严重程度,并在戊四唑 (PTZ) 诱发的急性癫痫模型中具有抗惊厥作用[1]

Z218484536 (2 mg/kg、4 mg/kg,腹腔注射,每日一次,3 天) 可降低 Kainic acid (HY-N2309) (KA) 诱发的 TLE 小鼠模型中海马 L-丝氨酸和 D-丝氨酸水平[1]

Z218484536 (2 mg/kg、4 mg/kg,腹腔注射,每日一次,7 周) 可抑制 TLE 小鼠的自发性癫痫发作[1]

Z218484536 (4 mg/kg,腹腔注射,7 天,每日一次) 不影响小鼠的情绪状态或运动能力[1]

Z218484536 (1 mg/kg,2 mg/kg,腹腔注射,2 周,每天一次,3.5 个月) 可降低食蟹猴 TLE 模型中的癫痫活动[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: KA mouse model of chronic TLE[1]
Dosage: 2 mg/kg, 4 mg/kg
Administration: i.p., 7  weeks, once a day
Result: Reduced SES frequency to 0.44  per day .
Not caused weight loss.
Animal Model: PTZ-induced acute model of seizures[1]
Dosage: 0.5 mg/kg, 1 mg/kg, 2 mg/kg, 4 mg/kg, 20 mg/kg
Administration: i.p., 3 days, once a day
Result: Delayed the onset of acute epilepsy .
The maximum anticonvulsant effect was observed at a concentration of 4 mg kg
分子量

247.23

Formula

C11H10FN5O

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

您最近查看的产品:

Your information is safe with us. * Required Fields.

   产品名称:

 

* 需求量:

* 客户姓名:

 

* Email:

* 电话:

 

* 公司或机构名称:

   留言给我们:

Bulk Inquiry

Inquiry Information

产品名称:
Z218484536
目录号:
HY-160955
需求量: