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UK-92480-西地那非 Sildenafil_代谢酶/蛋白酶-MedChemExpress LLC

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放大字体  缩小字体    发布日期:2019-09-02  来源:仪器信息网  作者:Mr liao  浏览次数:166
核心提示:更新时间:2019-07-01 09:36:1725 联系我们时请说明是91化工仪器网上看到的信息,谢谢! 产品简介 品牌 MedChemExpress (MCE) 货号 HY-15025 规格 10 mM * 1 mL;50 mg;100 mg 供货周期 现货 应用领域 生物产业 Sildenafil is a potent phosphodiesterase type 5 (PDE5) inhibitor with IC50 of 5.22 nM. 详细介绍 Sildenafil产品活性:Si

联系我们时请说明是91化工仪器网上看到的信息,谢谢!


产品简介 品牌 MedChemExpress (MCE) 货号 HY-15025 规格 10 mM * 1 mL;50 mg;100 mg 供货周期 现货 应用领域 生物产业     Sildenafil is a potent phosphodiesterase type 5 (PDE5) inhibitor with IC50 of 5.22 nM.
详细介绍 Sildenafil

产品活性:Sildenafil is a potent phosphodiesterase type 5 (PDE5) inhibitor with IC50 of 5.22 nM.

研究领域:metabolic Enzyme/Protease | Autophagy

作用靶点:Phosphodiesterase (PDE) | Autophagy

In Vitro: Pretreatment with 1 M Sildenafil potentiates the phosphorylation of ERK1/ERK2, an increase in the percentage of cells in S phase and cell proliferation, compared with serotonin stimulation alone (P 0.05). Pretreatment with 1 M Sildenafil citrate followed by serotonin stimulation leads to dramatic increase in OD value to 0.33, significantly different compared with serotonin stimulation alone (P 0.05). 1 M Sildenafil obviously enhances the upregulation of ERK1/ERK2 phosphorylation induced by serotonin.

In Vivo: In the dog model of erection, Sildenafil citrate significantly increases ICP and ICP/BP but shows no significant effect on BP compared with vehicle. Sildenafil treatment significantly decreases the number of TL+-cells at 10 but not 0.5 mg/kg. At this time point, cells positive for the M1-like marker COX-2+ are found in the ischemic core in PBS-treated animals, whereas they are mostly observed in the penumbra in 10 mg/kg (but not 0.5 mg/kg) Sildenafil-treated animals. In contrast, 8 days after pMCAo the number of microglia/macrophages stained by Iba-1 are significantly reduced by Sildenafil treatment (0.5 and/or 10 mg/kg dose). Sildenafil citrate has been reported to decrease flap necrosis in preclinical animal models by increasing the secretion of growth factors (FGF and VEGF), and histologically is shown to be effective in rat cavernous nerve architecture.

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