The holistic integration of virtual screening in drug discovery

被引:121
|
作者
Tanrikulu, Yusuf [1 ]
Krueger, Bjoern [1 ]
Proschak, Ewgenij [2 ]
机构
[1] Merz Pharmaceut GmbH, Chem R&D Drug Design, D-60318 Frankfurt, Germany
[2] Goethe Univ Frankfurt, Inst Pharmaceut Chem, D-60438 Frankfurt, Germany
关键词
HIGH-THROUGHPUT; GENETIC ALGORITHM; HIT LISTS; INHIBITORS; DOCKING; RECEPTOR; SHAPE; 5-LIPOXYGENASE; IDENTIFICATION; PERMEABILITY;
D O I
10.1016/j.drudis.2013.01.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
During the past decade, virtual screening (VS) has come of age. In this review, we document the evolution and maturation of VS from a rather exotic, stand-alone method toward a versatile hit and lead identification technology. VS campaigns have become fully integrated into drug discovery campaigns, evenly matched and complementary to high-throughput screening (HTS) methods. Here, we propose a novel classification of VS applications to help to monitor the advances in VS and to support future improvement of computational hit and lead identification methods. Several relevant VS studies from recent publications, in both academic and industrial settings, were selected to demonstrate the progress in this area. Furthermore, we identify challenges that lie ahead for the development of integrated VS campaigns.
引用
收藏
页码:358 / 364
页数:7
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