| CAS: | 87760-53-0 |
| 分子式: | C21H29N5O2 |
| 分子量: | 383.49 |
| 沸点: | 613.9±65.0 ℃ at 760 mmHg |
| 熔点: | 112-113.5℃ |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||||||||||||||||
| T875836 | MACKLIN | 坦度螺酮 | ≥98%（HPLC） | 583元/5mg; 1060元/10mg; 5940元/100mg; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
储存：2-8°C，避光 状态：白色到灰白色固体 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| T6704 | Sigma-Aldrich | Tandospirone | ≥98% (HPLC) | 1746.67元/5 MG; 6629.83元/25 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 包装 5, 25 mg in glass bottle 生化/生理作用 Tandospirone is a partial agonist at 5HT1A receptors. It significantly reduces haloperidol-induced bradykinesia in a dose-dependent manner. The potency of tandospirone is equal to that of buspirone and approximate half that of diazepam. The potency of tandospirone as a dopamine antagonistic is less than 1/4 that of buspirone. 特点和优势 This compound was developed by Dainippon Sumitomo. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here. 基本信息
产品性质
安全信息
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