• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Gisadenafil

CAS No. 334826-98-1

Gisadenafil ( UK-369003 )

产品货号. M26695 CAS No. 334826-98-1

Gisadenafil 是磷酸二酯酶 5 (PDE5) 的选择性抑制剂,IC50 为 3.6 nM,可防止 cGMP 降解。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥2774 有现货
10MG ¥4104 有现货
25MG ¥6398 有现货
50MG ¥8677 有现货
100MG ¥11250 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥3344 有现货

生物学信息

  • 产品名称
    Gisadenafil
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Gisadenafil 是磷酸二酯酶 5 (PDE5) 的选择性抑制剂,IC50 为 3.6 nM,可防止 cGMP 降解。
  • 产品描述
    Gisadenafil is a selective inhibitor of phosphodiesterase 5 (PDE5) with an IC50 of 3.6 nM and prevents degradation of cGMP.(In Vitro):In COS-7 cells, the IC50 of Gisadenafil for PDE1A is 9.1 μM, an approximately 2500-fold difference in selectivity.(In Vivo):In male Tat-transgenic mice, Gisadenafil (2 mg/kg; i.p.) restores the dilation of small (<25 μm) arterioles following hypercapnia, although it fails to restore full dilation of larger (>25 μm) vessels. Gisadenafil largely restores the normal increase in cortical flow following hypercapnia in Tat-tg mice (17.5% above baseline).
  • 体外实验
    Since some PDE5 inhibitors can also interact with PDE1 isotypes found within the cerebral vasculature, the specificity of Gisadenafil for PDE5 is confirmed. This is directly tested with recombinant PDE5A and PDE1A overexpressed in COS-7 cells. The IC50 of Gisadenafil for PDE5A is 3.6 nM. In contrast, the IC50 of Gisadenafil for PDE1A is 9.1 μM, an approximately 2500-fold difference in specificity.
  • 体内实验
    Gisadenafil (2 mg/kg; intraperitoneal injection; for 2 hours; male Tat-transgenic mice) treatment largely restores the normal increase in cortical flow following hypercapnia in Tat-tg mice (17.5% above baseline). Gisadenafil also restores the dilation of small (<25 μm) arterioles following hypercapnia, although it fails to restore full dilation of larger (>25 μm) vessels. Animal Model:Male Tat-transgenic (Tat-tg) mice (8 weeks old) exposed to hypercapnia Dosage:2 mg/kg Administration:Intraperitoneal injection; for 2 hours Result:Largely restored the normal increase in cortical flow following hypercapnia in Tat-tg mice (17.5% above baseline). Also restored the dilation of small (<25 μm) arterioles following hypercapnia.
  • 同义词
    UK-369003
  • 通路
    Angiogenesis
  • 靶点
    PDE
  • 受体
    Estrogen Receptor/ERR| Human Endogenous Metabolite
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    334826-98-1
  • 分子量
    519.62
  • 分子式
    C23H33N7O5S
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    CCOc1ncc(cc1-c1nc2c(CC)n(CCOC)nc2c(=O)[nH]1)S(=O)(=O)N1CCN(CC)CC1
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Choi HJ, et al. 4-Hydroxyestrone, an Endogenous Estrogen Metabolite, Can Strongly Protect Neuronal Cells Against Oxidative Damage. Sci Rep. 2020 Apr 29;10(1):7283.
产品手册
关联产品
  • GSK 256066 Trifluoro...

    一种有效的选择性 PDE4 抑制剂,对 PDE4B、A、C 和 D 的 pIC50 分别为 11.5、11.3、11.4 和 11.9。

  • RS-25344

    RS-25344 是一种有效的选择性磷酸二酯酶 (PDE) 4 抑制剂。

  • PQ-10

    PQ-10 是一种 PDE-10 抑制剂。 PQ-10 诱导大脑葡萄糖代谢模式,这可能是一种潜在的转化生物标志物。