EMT inhibitor-1
CAS No. 1638526-21-2
EMT inhibitor-1 ( —— )
产品货号. M26197 CAS No. 1638526-21-2
EMT抑制剂-1是Hippo、Wnt信号传导和TGF-巨噬细胞(TGF-)的抑制剂,具有抗肿瘤活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥2679 | 有现货 |
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| 10MG | ¥4256 | 有现货 |
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| 25MG | ¥6445 | 有现货 |
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| 50MG | ¥8677 | 有现货 |
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| 100MG | ¥11340 | 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 |
|
| 1 mL x 10 mM in DMSO | ¥2822 | 有现货 |
|
生物学信息
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产品名称EMT inhibitor-1
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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EMT抑制剂-1是Hippo、Wnt信号传导和TGF-巨噬细胞(TGF-)的抑制剂,具有抗肿瘤活性。
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产品描述EMT inhibitor -1 is an inhibitor of Hippo, Wnt signaling and TGF- macrophages (TGF-) with antitumor activity.(In Vitro):EMT inhibitor-1 (C19) inhibiting cancer cell migration, proliferation, and resistance to doxorubicin in vitro.EMT inhibitor-1 (C19) (0-10μM; 24 hours) is an inhibitor of of Hippo, TGF-β, and Wnt signaling pathways with antitumor activities.(In Vivo):EMT inhibitor-1 (C19) (intraperitoneal injection;?5-20 mg/kg) exerts strong antitumor activity in a mouse tumor model.?Mechanistically, EMT inhibitor-1 induces GSK3-β–mediated degradation of the Hippo transducer TAZ, through activation of the Hippo kinases Mst/Lats and the tumor suppressor kinase AMPK upstream of the degradation complex.C19 is dissolved in the vehicle solution (100 μL of DMEM containing 5% dimethyl sulfoxide).
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体外实验——
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体内实验——
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同义词——
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通路Wnt/Notch/Hedgehog
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靶点Wnt/beta/catenin
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受体PDE4| PDE5
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研究领域——
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适应症——
化学信息
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CAS Number1638526-21-2
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分子量319.2
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分子式C12H12Cl2N2O2S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (313.27 mM)
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SMILESOCCCCOc1nsnc1-c1ccc(Cl)c(Cl)c1
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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.Nagendran J, et al. Phosphodiesterase type 5 is highly expressed in the hypertrophied human right ventricle, and acute inhibition of phosphodiesterase type 5 improves contractility. Circulation. 2007 Jul 17;116(3):238-48.
产品手册
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