
PF-5274857 freebase
CAS No. 1373615-35-0
PF-5274857 freebase ( PF-5274857 | PF 5274857 | PF5274857 )
产品货号. M23528 CAS No. 1373615-35-0
PF-5274857 是一种有效的选择性刺猬信号通路抑制剂(IC50:5.8 nM,Ki:4.6 nM)。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥356 | 有现货 |
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5MG | ¥575 | 有现货 |
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10MG | ¥980 | 有现货 |
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25MG | ¥1798 | 有现货 |
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50MG | ¥2940 | 有现货 |
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100MG | ¥4366 | 有现货 |
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200MG | 获取报价 | 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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生物学信息
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产品名称PF-5274857 freebase
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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PF-5274857 是一种有效的选择性刺猬信号通路抑制剂(IC50:5.8 nM,Ki:4.6 nM)。
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产品描述PF-5274857 is an effective and selective hedgehog signaling pathway inhibitor (IC50: 5.8 nM and a Ki: 4.6 nM). PF-5274857 is a potentially attractive clinical candidate for the treatment of tumor types including brain tumors and brain metastasis driven by an activated Hh pathway.PF-5274857 was found to effectively penetrate the blood-brain barrier and inhibit Smo activity in the brain of primary medulloblastoma mice, resulting in improved animal survival rates. PF-5274857 was orally available and metabolically stable in vivo.
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体外实验PF-5274857 completely inhibits Shh-induced Hh pathway activity with an IC50 of 2.7±1.4 nM measured by the transcriptional activity of Smo downstream gene Gli1 in MEF cells.PF-5274857 shows less than 20% inhibition against a broad panel of protein kinases at 1 μM.
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体内实验PF-5274857 (1-30 mg/kg; p.o. once daily for 6 days) shows robust antitumor efficacy and correlation between PK and PD in medulloblastoma allograft mice models.PF-5274857 (10 mg/kg; i.h.) in the plasma is able to cross the blood-brain barrier in rats within 4 hours postdose.PF-5274857 (10-100 mg/kg; p.o. once daily for 4 days) is able to target Smo in the brain leading to the downregulation of Hh pathway activity in the brain tumor.PF-5274857 (30 mg/kg; p.o. once daily for 34 days) increases the survival rates of primary Ptch+/? p53?/? medulloblastoma mice.PF-5274857 (5-30 mg/kg; p.o.) exhibits the apparent volume of distribution of 5.6±0.5 L/kg and the half-life (T1/2) of 1.7±0.1 hours. Animal Model:Severe combined immunodeficient (SCID)-beige mice (6-8 weeks old) are genetically engineeredDosage:0, 1, 5, 10, 30 mg/kgAdministration:P.o. once daily for 6 days Result:Showed robust antitumor activity with an in vivo IC50 of 8.9±2.6 nM.Animal Model:Severe combined immunodeficient (SCID)-beige mice (6-8 weeks old)Dosage:0, 5, 10, 30 mg/kg (Pharmacokinetic Analysis)Administration:A single p.o.Result:The apparent volume of distribution of 5.6±0.5 L/kg; the half-life (T1/2) of 1.7±0.1 hours.
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同义词PF-5274857 | PF 5274857 | PF5274857
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通路Wnt/Notch/Hedgehog
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靶点Smoothened (Smo)
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受体smo
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研究领域——
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适应症——
化学信息
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CAS Number1373615-35-0
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分子量436.96
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分子式C20H25ClN4O3S
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纯度>98% (HPLC)
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溶解度DMSO:125 mg/mL?(286.07 mM;?Need ultrasonic)
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SMILESCC1=CC(=C(N=C1)C2=CC(=NC=C2Cl)N3CCN(CC3)C(=O)CCS(=O)(=O)C)C
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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.Zhou WJ, Chen J, Feng Y, Fan YP, Li Q, Fu J, Zhang P. [Inhibition of Cigarettes Smoke-induced Epithelial to Mesenchymal Transition by the SMO Inhibitor PF-5274857 in Beas-2b Epithelial Cells]. Sichuan Da Xue Xue Bao Yi Xue Ban. 2016 Jul;47(4):485-490. Chinese. PubMed PMID: 28591947.
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