• 13585831301
  • 021-59541103 021-60443211
  • 3004967995

AG-221 (Enasidenib)

  • 產(chǎn)品貨號(hào):CS-01Y63761
  • 產(chǎn)品價(jià)格:電議
  • 產(chǎn)品產(chǎn)地:進(jìn)口、國(guó)產(chǎn)
  • 包裝類型:5mg 25mg 100mg
  • 采購(gòu)熱度:191
  • 庫(kù)存:100
  • CAS號(hào):1446502-11-9
  • 方法:
  • 含量:>98.00%
  • 品牌名稱:莼試
  • 分子式:C19H17F6N7O
  • 分子量:473.37

簡(jiǎn)介內(nèi)容:質(zhì)量保證、價(jià)格優(yōu)惠

在線訂購(gòu)  免費(fèi)訂購(gòu)熱線:021-59541103 021-60443211

標(biāo)簽:AG-221 (Enasidenib) 

產(chǎn)品目錄

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聯(lián)系人:高小姐

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商品詳情購(gòu)物流程代測(cè)服務(wù)付款方式常見(jiàn)問(wèn)題

化學(xué)性質(zhì):                                                                                                             

規(guī)格

5mg 25mg 100mg

CAS

1446502-11-9

別名

2-methyl-1-((4-(6-(trifluoromethyl)pyridin-2-yl)-6-((2-(trifluoromethyl)pyridin-4-yl)amino)-1,3,5-triazin-2-yl)amino)propan-2-ol

化學(xué)名

 

分子式

C19H17F6N7O

分子量

473.37

溶解度

47.3mg/mL in DMSO

儲(chǔ)存條件

Store at -20°C

General tips

For obtaining a higher solubility , please warm the tube at 37 and shake it in the ultrasonic bath for a while.

Shipping Condition

Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request

 

產(chǎn)品描述:                                                                                                             

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].
References:
[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

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原創(chuàng)作者:上海莼試生物技術(shù)有限公司

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