共 22 条
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
相关论文
共 22 条