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 |
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| 10MG | ¥4104 | 有现货 |
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| 25MG | ¥6398 | 有现货 |
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| 50MG | ¥8677 | 有现货 |
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| 100MG | ¥11250 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥3344 | 有现货 |
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生物学信息
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产品名称Gisadenafil
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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
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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。
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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).
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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.
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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.
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同义词UK-369003
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通路Angiogenesis
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靶点PDE
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受体Estrogen Receptor/ERR| Human Endogenous Metabolite
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研究领域——
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适应症——
化学信息
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CAS Number334826-98-1
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分子量519.62
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分子式C23H33N7O5S
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纯度>98% (HPLC)
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溶解度——
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SMILESCCOc1ncc(cc1-c1nc2c(CC)n(CCOC)nc2c(=O)[nH]1)S(=O)(=O)N1CCN(CC)CC1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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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.
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