Comparison of topological descriptors for similarity-based virtual screening using multiple bioactive reference structures

被引:204
作者
Hert, J
Willett, P
Wilton, DJ
Acklin, P
Azzaoui, K
Jacoby, E
Schuffenhauer, A
机构
[1] Univ Sheffield, Krebs Inst Biomolec Res, Sheffield S10 2TN, S Yorkshire, England
[2] Univ Sheffield, Dept Informat Studies, Sheffield S10 2TN, S Yorkshire, England
[3] Novartis Inst Biomed Res, Discovery Technol, CH-4002 Basel, Switzerland
关键词
D O I
10.1039/b409865j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This paper reports a detailed comparison of a range of different types of 2D fingerprints when used for similarity-based virtual screening with multiple reference structures. Experiments with the MDL Drug Data Report database demonstrate the effectiveness of fingerprints that encode circular substructure descriptors generated using the Morgan algorithm. These fingerprints are notably more effective than fingerprints based on a fragment dictionary, on hashing and on topological pharmacophores. The combination of these fingerprints with data fusion based on similarity scores provides both an effective and an efficient approach to virtual screening in lead-discovery programmes.
引用
收藏
页码:3256 / 3266
页数:11
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