朱砂精酸
| 中文名称 | 朱砂精酸 |
|---|---|
| 中文同义词 | 朱砂精酸;化合物 T22669 |
| 英文名称 | cinnabarinic acid |
| 英文同义词 | cinnabarinic acid;2-Amino-3-oxo-3H-phenoxazine-1,9-dicarboxylic acid;Cinnabaric Acid;3H-Phenoxazine-1,9-dicarboxylic acid, 2-amino-3-oxo-;*Halothane Impurity 5 (Halothane EP Impurity E) |
| CAS号 | 606-59-7 |
| 分子式 | C14H8N2O6 |
| 分子量 | 300.22 |
| EINECS号 | |
| 相关类别 | 对照品;Amines;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals |
| Mol文件 | 606-59-7.mol |
| 结构式 |  |
朱砂精酸 性质
| 熔点 | >300°C |
|---|---|
| 密度 | 1.79 |
| 储存条件 | 2-8°C |
| 溶解度 | 二甲基亚砜：≥4mg/mL |
| 形态 | 粉末 |
| 颜色 | 红色至深红色 |
| 稳定性 | 从购买之日起 2 年内保持稳定。 DMSO 或 DMF 溶液可在 -20°C 下保存长达 1 个月。 |
|
mGluR4
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Cinnabarinic acid (0-100 μM) does not activate mGlu1, mGlu2, mGlu5, mGlu6, mGlu7, and mGlu8 receptors as shown by measurements of [ 3 H]InsP formation. In contrast, cinnabarinic acid acts as a partial agonist of mGlu4 receptors by increasing [ 3 H]InsP formation by approximately 35% at 100 μM, which is 5-fold less efficacious than ACPT-I in activating mGlu4 receptors in HEK293 cells transiently transfected with rat mGlu1, -2, -4, -5, -6, -7, or -8 receptors. Cinnabarinic acid (0-100 μM) reduces cAMP formation in a concentration-dependent manner with an excellent potency and efficacy. At 30 μM, cinnabarinic acid is effective at 30 μM, and substantially inhibits cAMP formation in cultured cerebellar granule cells.
安全信息
| WGK Germany | 3 |
|---|