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Canertinib dihydrochloride

    
99.90%

Canertinib dihydrochloride

源叶(MedMol)
S80594 一键复制产品信息
289499-45-2
C24H27Cl3FN5O3
558.86
卡纽替尼二盐酸盐;N-[4-[(3-氯-4-氟苯基)氨基]-7-(3-吗啉-4-基丙氧基)喹唑啉-6-基]丙-2-烯酰胺二盐酸盐;卡那替尼盐酸盐;卡奈替尼,卡纽替尼;卡纽替尼二盐酸盐 卡那替尼;卡奈替尼盐酸盐;卡奈替尼二盐酸盐;CANERTINIB DIHYDROCHLORIDE;N-[4-[(3-Chloro-4-fluorophenyl)amino]-7-(3-morpholin-4-ylpr
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S80594-5mg买3赠1
99.90%

¥160.00

6 - - - -
S80594-10mg买3赠1
99.90%

¥240.00

6 - - - -
S80594-25mg促销
99.90%

¥340.00 ¥272.00

7 - - - -
S80594-50mg促销
99.90%

¥410.00 ¥328.00

5 - - - -
S80594-100mg促销
99.90%

¥590.00 ¥530.00

5 - - - -
S80594-200mg
≥98%

¥880.00

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: Canertinib dihydrochloride (CI-1033 dihydrochloride) is a potent and irreversible EGFR inhibitor; inhibits cellular EGFR and ErbB2 autophosphorylation with IC50s of 7.4 and 9 nM. Canertinib dihydrochloride is active against vaccinia virus respiratory infection in mice
靶点: EGFR:7.4 nM (IC50);ErbB2:9 nM (IC50);EGFR
体内研究: Canertinib dihydrochloride (CI-1033 dihydrochloride) shows superior in vivo antitumor activity, giving growth delays in A431 xenografts exceeding 50 days following oral administration. The growth of human malignant melanoma xenografts, RaH3 and RaH5, in nude mice is significantly inhibited by i.p. injections of 40 mg/kg/day canertinib (Fig. 4). The anti-proliferative effect on melanoma xenografts is visible already within 4 days of treatment and further increased throughout the treatment period as observed through the differences in tumor volumes, reaching statistical significance within 18 days of treatment
参考文献: 1. Smaill JB, et al. Tyrosine kinase inhibitors. 17. Irreversible inhibitors of the epidermal growth factor receptor: 4-(phenylamino)quinazoline- and 4-(phenylamino)pyrido[3,2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions. J Med Chem. 2. Djerf Severinsson EA, et al. The pan-ErbB receptor tyrosine kinase inhibitor canertinib promotes apoptosis of malignant melanoma in vitro and displays anti-tumor activity in vivo. Biochem Biophys Res Commun. 2011 Oct 28;414(3):563-8. 3. McAndrews KM, et, al. Mechanisms associated with biogenesis of exosomes in cancer. Mol Cancer. 2019 Mar 30;18(1):52. 4. Smee DF, et, al. Progress in the discovery of compounds inhibiting orthopoxviruses in animal models. Antivir Chem Chemother. 2008;19(3):115-24.
溶解性: DMSO  :  62.5  mg/mL  (111.83  mM;  Need  ultrasonic)    H2O  :  25  mg/mL  (44.73  mM;  Need  ultrasonic)
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.789 ml 8.947 ml 17.894 ml
5 mM 0.358 ml 1.789 ml 3.579 ml
10 mM 0.179 ml 0.895 ml 1.789 ml
50 mM 0.036 ml 0.179 ml 0.358 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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