Hert Jérôme, Willett Peter, Wilton David J, Acklin Pierre, Azzaoui Kamal, Jacoby Edgar, Schuffenhauer Ansgar
Krebs Institute for Biomolecular Research and Department of Information Studies, University of Sheffield, Western Bank, Sheffield S10 2TN, UK.
Org Biomol Chem. 2004 Nov 21;2(22):3256-66. doi: 10.1039/B409865J. Epub 2004 Sep 29.
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.
本文报告了一系列不同类型的二维指纹在用于基于相似性的虚拟筛选并结合多个参考结构时的详细比较。使用MDL药物数据报告数据库进行的实验证明了编码使用摩根算法生成的圆形子结构描述符的指纹的有效性。这些指纹明显比基于片段字典、哈希和拓扑药效团的指纹更有效。将这些指纹与基于相似性分数的数据融合相结合,为先导化合物发现计划中的虚拟筛选提供了一种有效且高效的方法。