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S81341

Naquotinib

源叶(MedMol) ≥96%
  • 英文名:
  • Naquotinib
  • 别名:
  • CAS号:
  • 1448232-80-1
  • 分子式:
  • C30H42N8O3
  • 分子量:
  • 562.7063
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S81341-5mg ≥96% ¥677.00元 10 - - - EA 加入购物车
源叶(MedMol) S81341-10mg ≥96% ¥1185.00元 10 - - - EA 加入购物车
源叶(MedMol) S81341-25mg ≥96% ¥1625.00元 7 - - - EA 加入购物车
源叶(MedMol) S81341-50mg ≥96% ¥2817.00元 6 - - - EA 加入购物车
源叶(MedMol) S81341-100mg ≥96% ¥4789.00元 5 - - - EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: Naquotinib (ASP8273) is an orally available, mutant-selective and irreversible EGFR inhibitor; with IC50s of 8-33 nM toward EGFR mutants and 230 nM for EGFR.
  • 靶点: EGFR:230 nM (IC50);EGFRT790M;EGFRL858R/T790M;EGFRL858R;EGFRExon 19 deletion/T790M;EGFR
  • 体外研究:
    In assays using endogenously EGFR-dependent cells, Naquotinib inhibits the growth of PC-9(del ex19), HCC827(del ex19), NCI-H1975(del ex19/T790M) and PC-9ER(del ex19/T790M) with IC50s of 8-33 nM. Naquotinib selectively inhibits phosphorylation of EGFR and its down-stream signal pathway, ERK and Akt from 10nM in HCC827 and NCI-H1975 while inhibitory effects are only detected at 1000nM in A431.In NCI-H1650 (del ex19), Naquotinib inhibits cell growth with an IC50 value of 70nM while other EGFR-TKIs are only partially effective
  • 体内研究:
    Oral Naquotinib treatment dose dependently induces tumor regression in NCI-H1975 (L858R/T790M), HCC827 (del ex19) and PC-9 (del ex19) xenograft models. Dosing schedules does not affect the efficacy of Naquotinib. In an NCI-H1975 xenograft model, complete regression of tumor is achieved after 14-days of Naquotinib treatment. Complete regression is maintained in 50% of mice more than 85 days after cessation of Naquotinib treatment
  • 参考文献:
    1. Sakagami H, et al. ASP8273, a novel mutant-selective irreversible EGFR inhibitor, inhibits growth of non-small cell lung cancer (NSCLC) cells with EGFR activating and T790M resistance mutations. [abstract]. In: Proceedings of the 105th Annual Meeting of the American Association for Cancer Research; 2014 Apr 5-9; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2014;74(19 Suppl):Abstract nr 1728. doi:10.1158/1538-7445.AM2014-1728 2. Konagai S, et al. ASP8273 selectively inhibits mutant EGFR signal pathway and induces tumor shrinkage in EGFR mutated tumor models. [abstract]. In: Proceedings of the 106th Annual Meeting of the American Association for Cancer Research; 2015 Apr 18-22; Ph
  • 溶解性: Soluble  in  DMSO、Ethanol
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 1.777 ml 8.886 ml 17.771 ml
    5 mM 0.355 ml 1.777 ml 3.554 ml
    10 mM 0.178 ml 0.889 ml 1.777 ml
    50 mM 0.036 ml 0.178 ml 0.355 ml
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