化合物ZL006
| 中文名称 | 化合物ZL006 |
|---|---|
| 中文同义词 | 化合物ZL006;4-((3,5-二氯-2-羟基苄基)氨基)-2-羟基苯甲酸 |
| 英文名称 | 4-((3,5-Dichloro-2-hydroxybenzyl)amino)-2-hydroxybenzoic acid |
| 英文同义词 | 4-((3,5-Dichloro-2-hydroxybenzyl)amino)-2-hydroxybenzoic acid;ZL006;ZL 006;ZL006;Benzoic acid, 4-[[(3,5-dichloro-2-hydroxyphenyl)methyl]amino]-2-hydroxy-;iGluR,Ionotropic glutamate receptors,ZL006,ZL-006,Inhibitor,inhibit,ZL 006 |
| CAS号 | 1181226-02-7 |
| 分子式 | C14H11Cl2NO4 |
| 分子量 | 328.15 |
| EINECS号 | |
| 相关类别 | |
| Mol文件 | 1181226-02-7.mol |
| 结构式 |  |
化合物ZL006 性质
| 沸点 | 530.4±50.0 °C(Predicted) |
|---|---|
| 密度 | 1.617±0.06 g/cm3(Predicted) |
| 储存条件 | 2-8°C |
| 溶解度 | 在DMSO中的溶解度≥5mg/mL（加热至60°C） |
| 酸度系数(pKa) | 3.40±0.10(Predicted) |
| 形态 | 粉末 |
| 颜色 | 白色至棕褐色 |
ZL006 presents little cytotoxicity, and a growth inhibition of BCECs is not found at low concentration of 0.001, 0.01, 0.1, 1 and 10 μg/mL. The cytotoxicity of T7-P-LPs/ZL006 is significantly enhanced at the concentration of 10 μg/mL. Cellular uptake of ZL006 loads P-LPs and T7-P-LPs after incubation for 0.5 h at the concentrations range from 100 μg/mL to 600 μg/mL in BCECs. ZL006 does not inhibit the nNOS-PDZ/PSD-95-PDZ interaction, or perturb the nNOS β-finger.
Compared with P-LPs/ZL006 and free ZL006, T7-P-LPs/ZL006 exhibits a significant increase of drug accumulation in the brain tissue due to its better brain targeting delivery. Compared with free ZL006, P-LPs/ZL006 and T7-P-LPs/ZL006 exhibit a significant decrease of drug accumulation in the liver and kidney.
| 更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
|---|---|---|---|---|---|
| 2024/01/25 | HY-100456 | 化合物ZL006 ZL006 | 1181226-02-7 | 5mg | 700元 |
| 2024/01/25 | HY-100456 | 化合物ZL006 ZL006 | 1181226-02-7 | 10mM * 1mLin DMSO | 770元 |