Discovery of Novel Myc-Max Heterodimer Disruptors with a Three-Dimensional Pharmacophore Model

被引:66
作者
Mustata, Gabriela [1 ]
Follis, Ariele Viacava [3 ]
Hammoudeh, Dalia I. [3 ]
Metallo, Steven J. [3 ]
Wang, Huabo [4 ,5 ]
Prochownik, Edward V. [4 ,5 ]
Lazo, John S. [2 ]
Bahar, Ivet [1 ]
机构
[1] Univ Pittsburgh, Dept Computat Biol, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Pharmacol & Chem Biol, Pittsburgh, PA 15260 USA
[3] Georgetown Univ, Dept Chem, Washington, DC 20057 USA
[4] Univ Pittsburgh, Med Ctr, Childrens Hosp Pittsburgh, Hematol Oncol Sect, Pittsburgh, PA 15201 USA
[5] Univ Pittsburgh, Med Ctr, Dept Microbiol & Mol Genet, Pittsburgh, PA 15201 USA
关键词
C-MYC; MYC/MAX DIMERIZATION; INHIBITION; GALAHAD;
D O I
10.1021/jm801278g
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A three-dimensional pharmacophore model was generated utilizing a set of known inhibitors of c-Myc-Max heterodimer formation. The model successfully identified a set of structurally diverse compounds with potential inhibitory activity against c-Myc. Nine compounds were tested in vitro. and four displayed affinities in the micromolar range and growth inhibitory activity against c-Myc-overexpressing cells. These studies demonstrate the applicability of pharmacophore modeling to the identification of novel and potentially more puissant inhibitors of the c-Myc oncoprotein.
引用
收藏
页码:1247 / 1250
页数:4
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