1. Metabolic Enzyme/Protease
  2. Phosphodiesterase (PDE)
  3. Phosphodiesterase-IN-2

Phosphodiesterase-IN-2 (Compound C7) 是一种口服有效的磷酸二酯酶 10A (PDE10A) 选择性抑制剂,IC50 为 11.9 nM。Phosphodiesterase-IN-2 可以提高肝微粒体的稳定性,降低血脑屏障通透性。Phosphodiesterase-IN-2 在小鼠模型中表现出良好的药代动力学特征,可减轻 Isoprenaline (HY-108353) 诱导的心脏肥厚。

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Phosphodiesterase-IN-2 Chemical Structure

Phosphodiesterase-IN-2 Chemical Structure

CAS No. : 3047610-96-5

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  • 生物活性

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  • 参考文献

生物活性

Phosphodiesterase-IN-2 (Compound C7) is a selective, orally active inhibitor for phosphodiesterase 10A (PDE10A), with an IC50 of 11.9 nM. Phosphodiesterase-IN-2 improves the stability of liver microsomes, and lowers BBB permeability. Phosphodiesterase-IN-2 exhibits good pharmacokinetic characters, and attenuates isoprenaline (HY-108353)-induced cardiac hypertrophic in mouse models[1].

IC50 & Target

PDE10A

11.9 nM (IC50)

分子量

584.59

Formula

C32H27F3N6O2

CAS 号
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
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  • 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:
Phosphodiesterase-IN-2
目录号:
HY-161663
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