1. Metabolic Enzyme/Protease
  2. Phosphodiesterase (PDE)
  3. PDE4/5-IN-1

PDE4/5-IN-1 是一种选择性磷酸二酯酶 4/5 (PDE4/5) 双重抑制剂。PDE4/5-IN-1 可在功能上抑制 PDE5PDE4B2PDE4D2 的活性。PDE4/5-IN-1 可舒张离体大鼠前列腺组织,增强一氧化氮诱导的离体大鼠前列腺组织舒张作用,并降低 α-1 肾上腺素受体介导的离体大鼠前列腺组织收缩反应。PDE4/5-IN-1 可抑制人增生前列腺细胞的增殖。PDE4/5-IN-1 可用于良性前列腺增生的相关研究。

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PDE4/5-IN-1

PDE4/5-IN-1 Chemical Structure

CAS No. : 1807631-43-1

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

PDE4/5-IN-1 is a selective phosphodiesterase 4/5 (PDE4/5) dual inhibitor. PDE4/5-IN-1 functionally inhibits PDE5, PDE4B2, and PDE4D2 activity. PDE4/5-IN-1 relaxes isolated rat prostate tissue, enhances nitric oxide-induced relaxation in isolated rat prostate tissue, and reduces alpha-1 adrenoceptor-mediated contractile responses in isolated rat prostate tissue. PDE4/5-IN-1 inhibits proliferation of human hyperplastic prostate cells. PDE4/5-IN-1 can be used for the research of benign prostatic hyperplasia[1].

IC50 & Target[1]

PDE4B2

 

PDE4D2

 

PDE5

 

PDE6

 

PDE11

 

体外研究
(In Vitro)

PDE4/5-IN-1 (Compound VIII) (1-10 μM) 在无细胞实验中,于 1 μM 浓度下对 PDE4 (具体为 PDE4B2 和 PDE4D2) 和 PDE5 酶表现出双重抑制活性,且在 10 μM 浓度下还可抑制 PDE6PDE11[1]
PDE4/5-IN-1 (0.003 μM-3 μM) 可显著抑制 RWPE-1、BPH-1 和 WPMY-1 人前列腺细胞系的增殖,其中对 WPMY-1 基质细胞的作用最强[1]
PDE4/5-IN-1 (3 μM) 可显著增强 SNP (HY-B0564) 诱导的大鼠前列腺组织舒张作用,并降低 α-1 肾上腺素受体介导的收缩反应 [1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

433.41

Formula

C23H19N3O6

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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产品名称:
PDE4/5-IN-1
目录号:
HY-181774
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