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产品名称 | GABA receptor ↓ ↑ | GABAA receptor ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Niflumic Acid | ✔ | 98% | |||||||||||||||||
Ginkgolide A |
++
GABA receptor, Ki: 14.5 μM |
98% | |||||||||||||||||
Valproic acid sodium | ✔ | Autophagy,HDAC | 97% | ||||||||||||||||
Flumazenil | ✔ | 95% | |||||||||||||||||
Bemegride | ✔ | 98% | |||||||||||||||||
Bicuculline |
+++
GABAA receptor, IC50: 2 μM |
99% | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | Gamma aminobutyric acid (GABA), a naturally occurring amino acid, is the major inhibitory neurotransmitter in the cerebellum. AZD6280 is an α2/α3 subunit-selective GABAA receptor modulator with Ki values of 21 ± 5nM and 31 ± 17nM for α2 and α3, respectively. It also shows binding affinity to the α1 and α5 subunit with Ki values of 0.5 ± 0.2nM and 1680 ± 650nM, respectively. The in vitro efficacy of AZD6280 at α2 and α3 (32% and 34%, respectively) is 4- to 5-fold higher than that at α1 and α5 (8% and 7%, respectively)[1]. In primary mouse cortical neurons depleted with Disrupted-in-Schizophrenia-1 (DISC1), treatment with 0.1µM AZD6280 for 7 days rescued DISC1 knockdown-induced dendritic abnormalities[2]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.73mL 0.55mL 0.27mL |
13.65mL 2.73mL 1.36mL |
27.29mL 5.46mL 2.73mL |
CAS号 | 942436-93-3 |
分子式 | C20H22N4O3 |
分子量 | 366.41 |
SMILES Code | NC1=C(C(NCCC)=O)N=NC2=C1C=CC=C2C3=C(OC)C=CC(OC)=C3 |
MDL No. | MFCD21337368 |
别名 | |
运输 | 蓝冰 |
InChI Key | NVWCZRPXYVDQEE-UHFFFAOYSA-N |
Pubchem ID | 23630026 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Keep in dark place, sealed in dry, 2-8°C |
溶解方案 |
请根据您的动物给药指南选择适当的溶解方案。 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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