E1R,99.28%

产品编号:Bellancom-116463| CAS NO:1301211-78-8| 分子式:C13H16N2O2| 分子量:232.28

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货号 包装 价格 库存与货期 购买量 操作
Bellancom-116463
3500.00 杭州 北京(现货)
Bellancom-116463
5500.00 杭州 北京(现货)
Bellancom-116463
9900.00 杭州 北京(现货)
Bellancom-116463
16500.00 杭州 北京(现货)
Bellancom-116463
22500.00 杭州 北京(现货)

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E1R

产品介绍 E1R 是一种 sigma-1 受体的正变构调节剂 (Sig1R PAM),具有认知增强效果。
生物活性

E1R is a positive allosteric modulator of sigma-1 receptors (Sig1R PAM) with cognition-enhancing activity.

体外研究

The only target for E1R (inhibition or enhancement of radioligand binding exceeding 20%) is the sigma receptor. 10 μM E1R does not displace the radioligand, but instead increases the specific binding of a non-selective radioligand ([3H]1,3-di(2-tolyl)guanidine) for the sigma receptor by 38% in Jurkat cells.

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

体内研究

E1R demonstrates efficacy against scopolamine-induced cholinergic dysfunction in mice. Treatment with E1R (0.1-10 mg/kg; administered i.p. 60 min before the training session) significantly improves cognitive function in a dose-related manner in mice.

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

Animal Model: Male ICR and Balb/c mice weighed 23-25 g
Dosage: 0.1, 1 and 10 mg/kg
Administration: Administered i.p. 60 min before the training session
Result: Treatment at doses of 1 and 10 mg/kg increased retention latency by 194 and 211%, respectively, compared with the control group.
体内研究

E1R demonstrates efficacy against scopolamine-induced cholinergic dysfunction in mice. Treatment with E1R (0.1-10 mg/kg; administered i.p. 60 min before the training session) significantly improves cognitive function in a dose-related manner in mice.

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

Animal Model: Male ICR and Balb/c mice weighed 23-25 g
Dosage: 0.1, 1 and 10 mg/kg
Administration: Administered i.p. 60 min before the training session
Result: Treatment at doses of 1 and 10 mg/kg increased retention latency by 194 and 211%, respectively, compared with the control group.
性状Solid
溶解性数据
In Vitro: 

DMSO : 60 mg/mL (258.31 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 4.3051 mL 21.5257 mL 43.0515 mL
5 mM 0.8610 mL 4.3051 mL 8.6103 mL
10 mM 0.4305 mL 2.1526 mL 4.3051 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献

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