Mavoglurant is a structurally non-competitive mGlu5 receptor antagonist, has an IC50 of 30 nM in a functional assay with human mGluR5.
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描述 | Mavoglurant (AFQ056), a selective metabotropic glutamate receptor 5 (mGluR5) inhibitor, was tested for levodopa-induced dyskinesia (LID) in patients with Parkinson's Disease[3]. Negative modulation of mGluR5 activity improves eye gaze behavior and alters sympathetically-driven reactivity to faces in patients with FXS (fragile X syndrome) [4]. Chronic administration of a specific mGluR5 antagonist, Mavoglurant, was able to restore sociability behaviour of Fmr1 knockout mice to levels of wild type littermates[5]. In dogs, mavoglurant reduced the number of TLESRs (Transient lower esophageal sphincter relaxations) after intravenous and oral administration[6]. |
NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
NCT00414752 | Smoking Abstinence | Phase 1 | Completed | - | Germany ... 展开 >> Novartis Investigative Site Nuernberg, Germany 收起 << |
NCT00718341 | Fragile X Syndrome | Phase 2 | Completed | - | France ... 展开 >> Novartis Investigator Site Bron cedex, France, 69677 Italy Novartis Investigator Site Rome, Italy, 00168 Switzerland Novartis Investigator Site Lausanne, Switzerland, 1011 收起 << |
NCT01442259 | Mild Moderate ... 展开 >> or Severe Renal Impairment 收起 << | Phase 1 | Completed | - | Germany ... 展开 >> Novartis Investigative Site Kiel, Germany 收起 << |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
3.19mL 0.64mL 0.32mL |
15.95mL 3.19mL 1.60mL |
31.91mL 6.38mL 3.19mL |
CAS号 | 543906-09-8 |
分子式 | C19H23NO3 |
分子量 | 313.39 |
SMILES Code | O=C(N1CC[C@@]2([H])[C@@](C#CC3=CC=CC(C)=C3)(O)CCC[C@@]12[H])OC |
MDL No. | MFCD18633263 |
别名 | AFQ056 |
运输 | 蓝冰 |
InChI Key | ZFPZEYHRWGMJCV-ZHALLVOQSA-N |
Pubchem ID | 9926832 |
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 |
请根据您的动物给药指南选择适当的溶解方案。 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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