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RG 108
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
RG 108图片
包装与价格:
包装价格(元)
10mM (in 1mL DMSO)询价
10mg询价
25mg询价

RG 108 (N-Phthalyl-L-tryptophan) 是一种非核苷 DNA 甲基转移酶 (DNMTs) 抑制剂 (IC50\u003d115 nM),可阻断 DNMTs 活性位点。 RG 108 (N-Phthalyl-L-tryptophan) 导致肿瘤抑制基因的去甲基化和重新激活,但它不影响着丝粒卫星序列的甲基化。

Cell lines

The human promyelocytic leukemia HL-60 cells.

Preparation method

The solubility of this compound in DMSO is >10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37 ℃ for 10 minutes and/or shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.

Reaction Conditions

48 h; 50 μM

Applications

Cells were pretreated with 50 μM RG108 for 48 h and then after removal of the inhibitor cultivated with 1 μM RA for the next 4 days. Viable cell number was determined daily by counting in a hemocytometer after staining with 0.2% trypan blue. Cell cycle analysis of PI stained cells by flow cytometry demonstrated a slight decrease in the proportion of cells in S-phase (by 20% from control) after treatment with minor changes in G2/M.

产品描述

RG108 is a DNA methyltransferase (DMNT) inhibitor that enhanced reprogramming of OK-transduced MEFs in the presence of BIX. It is a small molecule that effectively blocked DNA methyltransferases in vitro and did not cause covalent enzyme trapping in human cell lines. DNA methylation regulates gene expression in normal and malignant cells. DNA methyltransferase inhibitors are able to reactivate epigenetically silenced genes. RG108 caused demethylation and reactivation of tumor suppressor genes, but it did not affect the methylation of centromeric satellite sequences. These results establish RG108 as a DNA methyltransferase inhibitor with fundamentally novel characteristics that will be particularly useful for the experimental modulation of epigenetic gene regulation.

References

Yan Shi, Caroline Desponts, Jeong Tae Do, Heung Sik Hahm, Hans R. Scholer, Sheng Ding. Induction of Pluripotent Stem Cells from Mouse Embryonic Fibroblasts by Oct4 and Klf4 with Small-Molecule Compounds. Cell Stem Cell. 2008; 3(5): 568 – 574.

Bodo Brueckner, Regine Garcia Boy, Pawel Siedlecki. Epigenetic Reactivation of Tumor Suppressor Genes by a Novel Small-Molecule Inhibitor of Human DNA Methyltransferases. Cancer Research. 2005; 65(14): 6305 – 11.

 
 
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