VU 0469650 hydrochloride

Pricing Availability   Qty
说明: Potent and selective negative allosteric modulator of mGlu1 receptors
化学名: 3-[(3R)-3-Methyl-4-(tricyclo[3.3.1.13,7]dec-1-ylcarbonyl)-1-piperazinyl]-2-pyridinecarbonitrile hydrochloride
纯度: ≥98% (HPLC)
说明书
引用文献
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文献 (5)

生物活性 for VU 0469650 hydrochloride

VU 0469650 hydrochloride is a potent and selective negative allosteric modulator of mGlu1 (IC50 = 99 nM). Exhibits >100-fold selectivity for mGlu1 over mGlu2-8 and 68 other GPCRs, ion channels, kinases and transporters. Brain penetrant.

技术数据 for VU 0469650 hydrochloride

分子量 400.94
公式 C22H28N4O.HCl
储存 Store at +4°C
纯度 ≥98% (HPLC)
CAS Number 1443748-47-7
PubChem ID 71680759
InChI Key YENVAZRENOYZGQ-GUIQYPADSA-N
Smiles O=C(N4CCN(C5=C(C#N)N=CC=C5)C[C@H]4C)C12CC(C3)CC(CC3C2)C1.Cl

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for VU 0469650 hydrochloride

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 40.09 100
ethanol 20.05 50

制备储备液 for VU 0469650 hydrochloride

以下数据基于产品分子量 400.94。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
1 mM 2.49 mL 12.47 mL 24.94 mL
5 mM 0.5 mL 2.49 mL 4.99 mL
10 mM 0.25 mL 1.25 mL 2.49 mL
50 mM 0.05 mL 0.25 mL 0.5 mL

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产品说明书 for VU 0469650 hydrochloride

参考文献 for VU 0469650 hydrochloride

参考文献是支持产品生物活性的出版物。

Lovell et al (2013) N-Acyl-N'-arylpiperazines as negative allosteric modulators of mGlu1: Identification of VU0469650, a potent and selective tool compound with CNS exposure in rats. Bioorg.Med.Chem.Lett. 23 3713 PMID: 23727046


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关键词: VU 0469650 hydrochloride, VU 0469650 hydrochloride supplier, VU0469650, hydrochloride, modulators, metabotropic, glutamate, receptor, mGlu1, mGluR1, allosteric, negative, potent, selective, NAMs, Glutamate, (Metabotropic), Group, I, Receptors, 5379, Tocris Bioscience

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