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IP7e
CAS No. 500164-74-9
IP7e ( IP 7e | IP-7e | isoxazolo-pyridinone 7e )
产品货号. M27887 CAS No. 500164-74-9
IP7e 是一种 Nurr1 激活剂,EC50 值为 3.9 nM。
纯度: >98% (HPLC)
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规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥3208 | 有现货 |
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10MG | ¥4771 | 有现货 |
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25MG | ¥7655 | 有现货 |
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50MG | ¥10368 | 有现货 |
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100MG | ¥14013 | 有现货 |
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500MG | ¥28026 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称IP7e
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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IP7e 是一种 Nurr1 激活剂,EC50 值为 3.9 nM。
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产品描述IP7e is a Nurr1 activator with an EC50 value of 3.9 nM.(In Vivo):IP7e(10 mg/kg) attenuates inflammation and neurodegeneration in spinal cords of EAE mice by an NF-kB pathway-dependent process. IP7e preventive treatment reduces the incidence and the severity of an MS murine model, i.e. experimental autoimmune encephalomyelitis (EAE).
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体外实验——
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体内实验IP7e (Isoxazolo-pyridinone 7e; 10 mg/kg; oral gavage; twice a day) preventive treatment reduces the incidence and the severity of a MS murine model, i.e. experimental autoimmune encephalomyelitis (EAE). IP7e attenuates inflammation and neurodegeneration in spinal cords of EAE mice by an NF-kB pathway-dependent process. Animal Model:Female C57BL/6J mice (6-8 week-old) with experimental autoimmune encephalomyelitis (EAE).Dosage:10 mg/kgAdministration:Oral gavage; twice a day; preventive administration (before the disease onset) from 7 to 23 d.p.i. and therapeutic (after the disease onset) from 21 to 36 d.p.i. Result:Preventive administration delayed the onset and reduces the incidence and severity of EAE, and decreased neuroinflammatory and histopathological alterations in the spinal cord of treated EAE mice. On the contrary, the course of EAE was not influenced by the therapeutic administration.
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同义词IP 7e | IP-7e | isoxazolo-pyridinone 7e
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通路Others
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靶点Other Targets
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受体ACMSD
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研究领域——
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适应症——
化学信息
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CAS Number500164-74-9
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分子量390.439
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分子式C23H22N2O4
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (256.13 mM)
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SMILESCOCCOCc1ccc(cc1)-c1cc2onc(-c3ccccc3)c2c(=O)n1C
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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.Pellicciari R, et al. α-Amino-β-carboxymuconate-ε-semialdehyde Decarboxylase (ACMSD) Inhibitors as Novel Modulators of De Novo Nicotinamide Adenine Dinucleotide (NAD+) Biosynthesis. J Med Chem. 2018 Feb 8;61(3):745-759.