DQP-997-74

目录号: GC73591纯度: >99.00%
DQP-997-74(化合物2i)是N-甲基-d-天冬氨酸受体(NMDAR)的选择性抑制剂,特异性靶向GluN2C/d(IC50:0.069μM和0.035μM),具有血脑屏障穿透性。

DQP-997-74
Cas No.: 2377187-09-0
规格价格库存数量操作
1 mg¥2,556.00现货
1

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产品描述 Description

DQP-997-74 (compound 2i) is a selective inhibitor of N-metl-d-aspartate receptor (NMDAR), specifically targeting GluN2C/D (IC50: 0.069 μM and 0.035 μM), with blood-brain barrier penetrability. Where DQP refers to didroquinoline-pyrazoline. DQP-997-74 acts synergistically with the agonist glutamate to exhibit time-dependent enhanced potency in inhibiting persynchronous activity driven by high-frequency excitatory synaptic transmission. DQP-997-74 reduces the number of epileptogenesis in a murine model of tuberous sclerosis complex (TSC)-induced epilepsy. DQP-997-74 can be used for research on NMDAR-related neurological diseases.

References:
[1]. D'Erasmo MP, et al. Development of a Didroquinoline-Pyrazoline GluN2C/2D-Selective Negative Allosteric Modulator of the N-Metl-d-aspartate Receptor. ACS Chem Neurosci. 2023 Sep 6;14(17):3059-3076..

产品文档 Product Documents

Purity:>99.00%

化学性质Chemical Properties

CAS 号
2377187-09-0
分子式
C28H19Cl2F2N3O4
分子量
570.37 g/mol
溶解性
DMSO : 100 mg/mL (175.32 mM; Need ultrasonic)
保存条件
-20°C
General tips
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 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol