VU0483605
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 5mg | ¥1590.00 | 10-15工作日发货 | |
| 10mg | ¥2703.00 | 10-15工作日发货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
VU0483605 is a selective positive allosteric modulator (PAM) of mGluR1 [1].
The metabotropic glutamate receptors (mGluRs), members of G-protein-coupled receptors, have been involved in a variety of functions in the central and peripheral nervous systems, such as learning, memory, anxiety, and the perception of pain. The mGluRs exist in pre- and postsynaptic neurons in synapses of the hippocampus, cerebellum, the cerebral cortex, as well as other parts of the brain and in peripheral tissues. Mice deficient in mGluR1 showed severe motor coordination and spatial learning deficient [2].
VU0483605 is a selective positive allosteric modulator (PAM) of mGluR1. VU0483605 displayed EC50 values of 0.39 and 0.36 μM at human and rat mGluR1 receptors, respectively. VU0483605 showed no activity against mGlu4 PAM with the EC50 of >10 μM. VU0483605 potentiated the response to glutamate in cells stably expressing mGlu1 and partially restored the reduction in glutamate-mediated calcium signaling in a mutant cell model of schizophrenia [1].
References:
[1] Cho H P, Garcia-Barrantes P M, Brogan J T, et al. Chemical modulation of mutant mGlu1 receptors derived from deleterious GRM1 mutations found in schizophrenics[J]. ACS chemical biology, 2014, 9(10): 2334-2346.
[2] Conquet F, Bashir Z I, Davies C H, et al. Motor deficit and impairment of synaptic plasticity in mice lacking mGluR1[J]. Nature, 1994, 372(6503): 237.
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 1623101-11-0 |
| 分子式 | C20H10Cl3N3O3 |
| 分子量 | 446.7 |
| 化学名称 | 3-chloro-N-[3-chloro-4-(4-chloro-1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]-2-pyridinecarboxamide |
| 溶解度 | ≤20mg/ml in DMSO;20mg/ml in dimethyl formamide |
| SMILES | O=C(c1ncccc1Cl)Nc(cc1)cc(Cl)c1N(C(c1cccc(Cl)c11)=O)C1=O |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | VU0483605 是一种强效的脑穿透 mGlu1 受体正异位调节剂(PAM)。VU0483605 在人和大鼠体内均显示出卓越的 mGlu1 PAM 活性,其 EC50 值分别为 390 和 356 nM。 |



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