| CAS: | 1135243-19-4 | |||||
| 分子式: | C18H20N6O3S2 | |||||
| 分子量: | 432.52 | |||||
| 沸点: | 689.3±65.0°C at 760 mmHg | |||||
| 英文名称: |
|
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||||||||||||||||||||||
| V890452 | MACKLIN | N-(3-氧代-3-(4-(吡啶-4-基)哌嗪-1-基)丙基)苯并[c][1,2,5]噻二唑-4-磺酰胺 | 95% | 119元/25mg; 340元/100mg; 580元/250mg; 1569元/1g; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
储存：-20°C，干燥密封 状态：黄色粉末 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| V3765 | Sigma-Aldrich | VU0255035 hydrate | ≥98% (HPLC) | 1843.44元/5 MG; 5933.09元/25 MG; | 展开 | ||||||||||||||||||||||||||||||||||||||||||||||||
产品说明 包装 5, 25 mg in glass bottle 生化/生理作用 VU0255035 is the first highly selective antagonist at the orthosteric site of the M1 receptor (75-fold selective for M1 relative to other muscarininc subtypes and devoid of activity at other GPCRs, ion channels, transporters and kinases). There are no highly selective M1 muscarinic receptor antagonists. The existing non-selective drugs do not permit direct evaluation of the role of M1 receptors in CNS fucntions and do not premit therapeutic targeting of M1 receptors in various disease states in which M1 receptors are implicated (epilepsy, Parkinson′s disease, attention and cognitive disorders, dystonia, etc). 特点和优势 This compound is a featured product for Neuroscience research. Click here to discover more featured Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm. 基本信息
产品性质
安全信息
| |||||||||||||||||||||||||||||||||||||||||||||||||||||
m.cnreagent.com
