全部分类
  • AG-221 (Enasidenib)
AG-221 (Enasidenib)的可视化放大

AG-221 (Enasidenib)

An inhibitor of mutant IDH2

此产品仅用于科学研究,我们不为任何个人用途提供产品和服务

AG-221 (Enasidenib)的二维码
  • 库存: 现货
可选规格
  • 包装
    价格
    促销价
    数量
  • 5mg
    ¥475.00
    380.00
    - +
  • 25mg
    ¥1737.00
    1390.00
    - +
  • 100mg
    ¥4525.00
    3620.00
    - +
已选 0 0
金额: ¥0.00
首页 收藏
  • 货号: ajci10536
  • CAS: 1446502-11-9
  • 别名: 恩西地平; AG-221
  • 分子式: C19H17F6N7O
  • 分子量: 473.37
  • 纯度: >98%
  • 溶解度: ≥ 47.3mg/mL in DMSO
  • 储存: Store at -20°C
  • 库存: 现货

Background

IC50: ~16 nM for IDH2 R140Q mutant


AG-221 (Enasidenib) is a mutant isocitrate dehydrogenase 2 (IDH2) inhibitor.


The somatic mutations of IDH1 and IDH2 are found in patients with acute myeloid leukemia. Leukemia-associated IDH1/2 mutations lead to aberrant accumulation of the oncometabolite 2-hydroxyglutarate (2-HG).


In vitro: AG-221 was found to be able to reduce 2-HG levels by >90%, reverse in-vitro histone and DNA hypermethylation, and induce differentiation in leukemia cell model as well. In addition, a dose dependent proliferative burst of the human specific CD45+ blast cells was observed by the treatment of AG-221, as measured by the expression of CD11b, CD14, CD15 and cell morphology [1].


In vivo: The efficacy of AG-221 in a primary human AML xenograft model with the IDH2 R140Q mutation was studied, and the results showed that AG-221 could reduce 2-HG in the plasma, bone marrow, and urine of engrafted mice potently. In addition, the treatment of AG-221 could also induce a significant and dose dependent survival benefit as demonstrated by that all mice in the high dose treatment of AG-221 survived to the end of study [1].


Clinical trial: A phase 1, multicenter, dose-escalation, safety, PK, PD, and clinical activity study of AG-221 in patients with advanced hematologic malignancies with an IDH2 mutation has been conducted [2].

参考文献:
[1] Kate Ellwood-Yen, Fang Wang, Jeremy Travins, Yue Chen, Hua Yang, Kim Straley, Sung Choe, Marion Dorsch, Sam Agresta, David Schenkein, Scott Biller, Michael Su.? AG-221 offers a survival advantage in a primary human IDH2 mutant AML xenograft model. [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 3116. doi:10.1158/1538-7445.AM2014-3116
[2] https://clinicaltrials.?gov/ct2/show/NCT02577406term=Enasidenib&rank=1

没有评价数据

温馨提示 ×
商品已成功加入购物车!
购物车共 0 件商品
去购物车结算