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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 | BPDBA is a selective and non-competitive inhibitor of the betaine/GABA transporter (BGT-1), with IC50s of 20 μM and 35 μM for human BGT-1 and mouse GAT2, respectively. BPDBA is predicted to have excellent oral absorption and blood-brain-barrier permeability properties [1]. |
| 计算器 | ||||
| 存储液制备 | ![]() | 1mg | 5mg | 10mg |
1 mM 5 mM 10 mM | 2.75mL 0.55mL 0.28mL | 13.76mL 2.75mL 1.38mL | 27.53mL 5.51mL 2.75mL | |
| CAS号 | 312281-74-6 |
| 分子式 | C19H20Cl2N2O |
| 分子量 | 363.28 |
| SMILES Code | O=C(NC1CCN(CC2=CC=CC=C2)CC1)C3=CC=C(Cl)C=C3Cl |
| MDL No. | N/A |
| 别名 | |
| 运输 | 蓝冰 |
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 | DMSO: 105 mg/mL(289.03 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
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