Specific stabilization of DNA triple helices by indolo[2,1-b]quinazolin-6,12-dione derivatives

Grace Shiahuy Chen, Bhalchandra V. Bhagwat, Pei Yin Liao, Hui Ting Chen, Shwu Bin Lin, Ji Wang Chern*

*此作品的通信作者

研究成果: Article同行評審

13 引文 斯高帕斯(Scopus)

摘要

Derivatives of indolo[2,1-b]quinazolinone containing aminoalkylamino side chains were synthesized as specific DNA triplex stabilizing agents. The aminoalkylamino side chains are essential for triplex stabilization. The position-8 fluorine atom or a methyl group to the nitrogen adjacent to the planar core can enhance triplex stability by 6 °C and the effect is additive. Conformational analysis reveals that the orientation of the side chain underlies the ability of this compound to stabilize a DNA triplex.

原文English
頁(從 - 到)1769-1772
頁數4
期刊Bioorganic and Medicinal Chemistry Letters
17
發行號6
DOIs
出版狀態Published - 15 3月 2007

指紋

深入研究「Specific stabilization of DNA triple helices by indolo[2,1-b]quinazolin-6,12-dione derivatives」主題。共同形成了獨特的指紋。

引用此