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Icotinib

    
99.80%

Icotinib

源叶(MedMol)
S81502 一键复制产品信息
610798-31-7
  C22H21N3O4
391.42
BPI-2009H;[1,4,7,10]Tetraoxacyclododecino[2,3-g]quinazolin-4-amine, N-(3-ethynylphenyl)-7,8,10,11,13,14-hexahydro-
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S81502-1mg买3赠1
99.80%

¥590.00

1 - - - -
S81502-2mg买3赠1
99.80%

¥830.00

3 - - - -
S81502-5mg买3赠1
99.80%

¥1050.00

1 - - - -
S81502-10mg
≥98%

¥1570.00

货期:2-3天 - - - -
S81502-25mg
≥98%

¥3100.00

货期:2-3天 - - - -
产品介绍 参考文献(1篇) 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Icotinib (BPI-2009) is a potent and specific EGFR inhibitor with an IC50 of 5 nM; also inhibits mutant EGFRL858R, EGFRL858R/T790M, EGFRT790M and EGFRL861Q.
靶点: EGFR:5 nM (IC50);EGFRL858R;EGFRL858R/T790M;EGFRT790M;EGFRL861Q;EGFR
体内研究: Icotinib exhibits potent dose-dependent antitumor effects in nude mice carrying a variety of human tumor-derived xenografts. The drug is well tolerated at doses up to 120 mg/kg/day in mice without mortality or significant body weight loss during the treatment. Icotinib inhibits tumor growth at a rate of 25.2%, 45.6% and 51.5% in the A431 cell line groups; 3.4%, 25.9% and 31.0% in the A549 cell line groups; 49.4%, 52.6% and 67.4% in the H460 cell line groups, and 30.3%, 36.4% and 46.5% in the HCT8 cell line groups, at 30, 60 and 120 mg/kg/dose, respectively
参考文献: 1. Tan F, et al. Icotinib (BPI-2009H), a novel EGFR tyrosine kinase inhibitor, displays potent efficacy in preclinical studies. Lung Cancer. 2012 May;76(2):177-82.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.555 ml 12.774 ml 25.548 ml
5 mM 0.511 ml 2.555 ml 5.11 ml
10 mM 0.255 ml 1.277 ml 2.555 ml
50 mM 0.051 ml 0.255 ml 0.511 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。

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摩尔浓度计算器

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