LF3
目录号: PL13239 纯度: ≥99%
CAS No. :664969-54-4
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PL13239-5mg 5mg ¥964.00 请登录
PL13239-10mg 10mg ¥1253.00 请登录
PL13239-25mg 25mg ¥2812.00 请登录
PL13239-50mg 50mg ¥4500.00 请登录
PL13239-100mg 100mg ¥8357.00 请登录
PL13239-200mg 200mg 询价 询价
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PL13239-10mM*1mLinDMSO 10mM*1mLinDMSO ¥1060.00 请登录
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中文名称
LF3
中文别名
LF3
英文名称
LF3
英文别名
LF3;LF-3;N-[4-(Aminosulfonyl)phenyl]-4-(3-phenyl-2-propen-1-yl)-1-piperazinecarbothioamide;N-[4-(Aminosulfonyl)phenyl]-4-(3-phenyl-2-propenyl)-1-piperazinecarbothioamide;4-[(2E)-3-phenylprop-2-en-1-yl]-N-(4-sulfamoylphenyl)piperazine-1-carbothioamide;1-Piperazinecarbothioamide, N-[4-(aminosulfonyl)phenyl]-4-(3-phenyl-2-propen-1-yl)-;s8474;STK143540;4-[(E)-3-phenylprop-2-enyl]-N-(4-sulfamoylphenyl)piperazine-1-carbothioamide;LF3, >=98% (HPLC);ST50763308;A16851;4-({[4-((2E)-3-phenyl
Cas No.
664969-54-4
分子式
C20H24N4O2S2
分子量
416.56
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
LF3是β-Catenin/TCF4相互作用的拮抗剂,具有抗肿瘤活性。IC50值为1.65 μM。
生物活性
LF3 is an antagonist of the β-Catenin/TCF4 interaction with antitumor activity; has an IC 50 of 1.65 μM.
性状
Solid
IC50 & Target[1][2]
IC50: 1.65 μM (β-Catenin/TCF4, AlphaScreen), 1.82 μM (β-Catenin/TCF4, ELISA)
体外研究(In Vitro)
LF3 inhibits Wnt/β-catenin signals in cells with exogenous reporters and in colon cancer cells with endogenously high Wnt activity. LF3 also suppresses features of cancer cells related to Wnt signaling, including high cell motility, cell-cycle progression, and the overexpression of Wnt target genes. However, LF3 does not cause cell death or interfere with cadherin-mediated cell-cell adhesion. Remarkably, the self-renewal capacity of cancer stem cells is blocked by LF3 in concentration-dependent manners. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
LF3 reduces tumor growth and induces differentiation in a mouse xenograft model of colon cancer. Tumor growth is significantly reduced when mice with GFP cells are treated with LF3 at 50 mg/kg. LF3 treatment does not disturb the normal histology of the gut of mice. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Fang L, et al. A Small-Molecule Antagonist of the β-Catenin/TCF4 Interaction Blocks the Self-Renewal of Cancer Stem Cells and Suppresses Tumorigenesis. Cancer Res. 2016 Feb 15;76(4):891-901.
溶解度数据
In Vitro: DMSO : 250 mg/mL (600.15 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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