PF429242 dihydrochloride
CAS No. 2248666-66-0
PF429242 dihydrochloride ( —— )
产品货号. M26372 CAS No. 2248666-66-0
PF429242 diHClide 可以可逆地抑制 S1P(IC50 为 175 nM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥377 | 有现货 |
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| 5MG | ¥677 | 有现货 |
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| 10MG | ¥1017 | 有现货 |
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| 25MG | ¥2120 | 有现货 |
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| 50MG | ¥3060 | 有现货 |
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| 100MG | ¥4401 | 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 | ¥744 | 有现货 |
|
生物学信息
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产品名称PF429242 dihydrochloride
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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PF429242 diHClide 可以可逆地抑制 S1P(IC50 为 175 nM)。
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产品描述PF429242 dihydrochloride can reversibly inhibit S1P (IC50 of 175 nM).(In Vitro):10 μM PF-429242 down-regulates the signal from an SRE-luciferase reporter gene in human embryonic kidney 293 cells and the expression of endogenous SREBP target genes in cultured HepG2 cells. In HepG2 cells, PF-429242 inhibits cholesterol synthesis, with an IC50 of 0.5 μM. PF-429242 treatment also shows suppressive effects on DENV2 yields in the cultured fluids of human-derived HEK-293, Hep G2, and non-human-primate derived LLC-MK2 cells. PF-429242 has potent antiviral against LCMV and LASV .(In Vivo):PF-429242 inhibits the expression of hepatic SREBP target genes, and the hepatic rates of cholesterol and fatty acid synthesis are reduced In mice.
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体外实验10 μM PF-429242 inhibits endogenous SREBP processing in Chinese hamster ovary cells. PF-429242 also down-regulates the signal from an SRE-luciferase reporter gene in human embryonic kidney 293 cells and the expression of endogenous SREBP target genes in cultured HepG2 cells. In HepG2 cells, PF-429242 inhibits cholesterol synthesis, with an IC50 of 0.5 μM. The addition of PF-429242 (30 μM) shows statistically significant suppression of infectious viral titers and viral RNA copies in the cell culture fluids. PF-429242 treatment also shows suppressive effects on DENV2 yields in the cultured fluids of human-derived HEK-293, Hep G2, and non-human-primate derived LLC-MK2 cells. PF-429242 efficiently prevents the processing of GPC from the prototypic arenavirus lymphocytic choriomeningitis virus (LCMV) and LASV, which correlates with the compound's potent antiviral activity against LCMV and LASV in cultured cells.
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体内实验In mice treated with PF-429242 for 24 h, the expression of hepatic SREBP target genes is suppressed, and the hepatic rates of cholesterol and fatty acid synthesis are reduced.
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同义词——
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通路GPCR/G Protein
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靶点S1P Receptor
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受体——
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研究领域——
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适应症——
化学信息
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CAS Number2248666-66-0
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分子量482.49
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分子式C25H37Cl2N3O2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : ≥ 83.3 mg/mL (172.65 m)
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SMILESO=C(N(CCC1=CC=CC=C1OC)[C@H]2CNCC2)C3=CC=C(CN(CC)CC)C=C3.[H]Cl.[H]Cl
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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.Ma?aszyńska-Olkiewicz E, Lipski L, Gwie?dziński Z, Szyszymar B. [New method of treatment of rosacea with metronidazole and Anavenol or Venacorn]. Przegl Dermatol. 1981 May-Jun;68(3):395-8. Polish.
产品手册
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