企业信息
17
  • 入驻时间: 2008-08-20
  • 联系人:客户经理
  • 电话:400-968-7988
  • 联系时,请说明易展网看到的
  • Email:fuwu@bioleaf.com
产品详情
  • 产品名称:RG108---DNAMethyltransferaseInhibitor

  • 产品型号:M60176-2s
  • 产品厂商:其它品牌
  • 产品价格:65
  • 折扣价格:0
  • 产品文档:
你添加了1件商品 查看购物车
简单介绍:
RG108---DNAMethyltransferaseInhibitor
详情介绍:
Product Information
Molecular Weight: 334.33
Formula: C19H14N2O4
Purity: ≥98%
CAS#: 48208-26-0
Solubility: DMSO up to 100 mM
Chemical Name: (S)-2-(1,3-dioxoisoindolin-2-yl)-3-(1H-indol-3-yl)propanoic acid
Storage: Powder: 4oC 1 year. DMSO: 4oC 3 month; -20oC 1 year.

Biological Activity:

RG108 is a potent, selective and cell permeable inhibitor of DNA methyltransferase. Unlike 5-azaC, RG108 is not a nucleoside and therefore does not modify DNA. It binds to the enzyme active site and inhibits DNMT enzymatic activity with an IC50 ~ 115 nM. It inhibits DNA methylation in human cancer cell lines in vitro without detectable toxicity. Treatment with RG108 results in the demethylation of genomic DNA and can reactivate epigenetically silenced tumor suppressor genes. It has been shown to improve the reprogramming efficiency of mouse embryonic fibroblasts (MEFs) into induced pluripotent stem (iPS) cells. RG108 can potentially be used to maintain embryonic stem (ES) cells in an undifferentiated state as well as replace transcription factors in both mouse and human cell reprogramming.


How to Use:

  • In vitro: RG108 was used at 10-100 µM final concentration in various in vitro assays.
  • In vivo: n/a

Reference:

  1. 1. Brueckner B, et al. Epigenetic reactivation of tumor suppressor genes by a novel small-molecule inhibitor of human DNA methyltransferases. (2005) Cancer Res. 65(14):6305-11.
  2. 2. Stresemann C, et al. Functional diversity of DNA methyltransferase inhibitors in human cancer cell lines. (2006) Cancer Res. 66(5):2794-800.
  3. 3. Schirrmacher E, et al. Synthesis and in vitro evaluation of biotinylated RG108: a high affinity compound for studying binding interactions with human DNA methyltransferases. (2006) Bioconjug Chem. 17(2):261-6.
  4. 4. Shi Y, et al. Induction of pluripotent stem cells from mouse embryonic fibroblasts by Oct4 and Klf4 with small-molecule compounds. (2008) Cell Stem Cell. 3(5):568-74.
  5. 5. Pasha Z, et al. Efficient non-viral reprogramming of myoblasts to stemness with a single small molecule to generate cardiac progenitor cells. (2011) PLoS One. 6(8):e23667.


Products are for research use only. Not for human use. 

标题:
内容:
联系人:
联系电话:
Email:
公司名称:
联系地址:
 
 
注:1.可以使用快捷键Alt+S或Ctrl+Enter发送信息!
2.如有必要,请您留下您的详细联系方式!
相关文章

沪公网安备 31011202007337号