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JK184

    
99.90%

N-(4-ethoxyphenyl)-4-(2-methylimidazo[1,2-a]pyridin-3-yl)-1,3-thiazol-2-amine

源叶(MedMol)
S84887 一键复制产品信息
315703-52-7
C19H18N4OS
350.45
MFCD01044465
N-(4-ethoxyphenyl)-4-(2-methylimidazo[1,2-a]pyridin-3-yl)-2-thiazolamine; N-(4-Ethoxyphenyl)-4-(2-methylimidazo[1,2-a]pyridin-3-yl)thiazol-2-amine; HH SIGNALING ANTAGONIST VII;
货号 规格 价格 上海 北京 武汉 南京 购买数量
S84887-2mg一口价
99.90% ¥140.00 5 - - -
S84887-5mg一口价
99.90% ¥224.00 6 - - -
S84887-10mg一口价
99.90% ¥336.00 6 - - -
S84887-25mg一口价
99.90% ¥536.00 5 - - -
S84887-50mg
99.90% ¥1000.00 5 - - -
S84887-100mg
≥99% ¥1500.00 货期:2-3天 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: JK184 is a potent Hedgehog (Hh) pathway inhibitor with IC50 of 30 nM in mammalian cells.
靶点: IC50: 30 nM (Hedgehog);Hedgehog/Smoothened
体内研究: JK184 (5 mg/kg, injected intravenously) exhibits good anti-proliferative activity in subcutaneous Panc-1 and BxPC-3 tumor models, and is a good candidate as antitumor drug targeted Hh signaling. However, JK184 has a poor pharmacokinetic profile and bioavailability
参考文献: 1. Zhang N, et al. Biodegradable polymeric micelles encapsulated JK184 suppress tumor growth through inhibiting Hedgehog signaling pathway. Nanoscale. 2015 Feb 14;7(6):2609-24. 2. Colavito SA, et al. Significance of glioma-associated oncogene homolog 1 (GLI1) expression in claudin-low breast cancer and crosstalk with the nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) pathway. Breast Cancer Res. 2014 Sep 25;16
溶解性: Soluble  in  DMSO
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.853 ml 14.267 ml 28.535 ml
5 mM 0.571 ml 2.853 ml 5.707 ml
10 mM 0.285 ml 1.427 ml 2.853 ml
50 mM 0.057 ml 0.285 ml 0.571 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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