1. GPCR/G Protein Neuronal Signaling
  2. mGluR
  3. VU6024578

VU6024578 (BI02982816) 是口服有效的代谢型谷氨酸受体 (mGluR1) 选择性正变构调节剂 (PAM),可激活人类 mGluR1 和大鼠 mGluR1EC50 分别为 54 nM 和 46 nM。VU6024578 在大鼠 amphetamine 诱发的多动症模型和 MK-801 (HY-15084B) 诱发的新物体识别 (NOR) 模型中表现出抗精神病活性。VU6024578 具有血脑屏障通透性。

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VU6024578 Chemical Structure

VU6024578 Chemical Structure

1.  客户无需承担相应的运输费用。

2.  同一机构(单位)同一产品试用装仅限申领一次,同一机构(单位)一年内

     可免费申领三个不同产品的试用装。

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

VU6024578 (BI02982816) is a selective, orally active positive allosteric modulator (PAM) for metabotropic glutamate receptor (mGluR1), that activates human mGluR1 and rat mGluR1 with EC50 of 54 nM and 46 nM. VU6024578 exhibits antipsychotic activity in rats amphetamine-induced hyperactivity models and MK-801 (HY-15084B)-induced novel object recognition (NOR) models. VU6024578 is blood brain barrier penetrable[1].

IC50 & Target

rat mGluR1

46 nM (EC50)

Human mGluR1

54 nM (EC50)

分子量

395.84

Formula

C20H18ClN5O2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
VU6024578
目录号:
HY-170499
需求量: