Fenobam
CAS No. 57653-26-6
Fenobam ( —— )
产品货号. M26686 CAS No. 57653-26-6
Fenobam 显示反向激动剂活性,可阻断 mGlu5 受体基础活性 (IC50: 84 nM)。非诺班具有抗焦虑活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥567 | 有现货 |
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| 10MG | ¥960 | 有现货 |
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| 25MG | ¥1646 | 有现货 |
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| 50MG | ¥2381 | 有现货 |
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| 100MG | ¥3195 | 有现货 |
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| 200MG | ¥4383 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥661 | 有现货 |
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生物学信息
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产品名称Fenobam
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Fenobam 显示反向激动剂活性,可阻断 mGlu5 受体基础活性 (IC50: 84 nM)。非诺班具有抗焦虑活性。
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产品描述Fenobam shows inverse agonist activity which blocks the mGlu5 receptor basal activity(IC50: 84 nM). Fenobam has anxiolytic activity. Fenobam is a selective and non-competitive mGluR5 antagonist acting at an allosteric modulatory site (Kd values are 54 and 31 nM for rat and human recombinant mGlu5 receptors, respectively).(In Vivo):Fenobam sulfate (30-60 mg/kg; p.o.) inhibited cocaine self-administration significantly .
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体外实验——
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体内实验Animal Model:Male Long-Evans rats (250-300 g)Dosage:30-60 mg/kg Administration:P.o.Result:Inhibited self-administration
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同义词——
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通路Neuroscience
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靶点GluR
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受体MAGL
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研究领域——
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适应症——
化学信息
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CAS Number57653-26-6
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分子量266.69
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分子式C11H11ClN4O2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (374.98 mM)
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SMILESCN1CC(=O)N=C1NC(=O)Nc1cccc(Cl)c1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Shuhei Ikeda, et al. Design and Synthesis of Novel Spiro Derivatives as Potent and Reversible Monoacylglycerol Lipase (MAGL) Inhibitors: Bioisosteric Transformation from 3-Oxo-3,4-dihydro-2 H-benzo[ b][1,4]oxazin-6-yl Moiety. J Med Chem. 2021 Aug 12;64(15):11014-11044.
产品手册
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