Molecular descriptors in chemoinformatics, computational combinatorial chemistry, and virtual screening

被引:188
作者
Xue, L
Bajorath, J
机构
[1] New Chem Entities, Comp Aided Drug Discovery, Bothell, WA 98011 USA
[2] Univ Washington, Dept Biol Struct, Seattle, WA 98195 USA
[3] Univ Washington, New Chem Entities, Seattle, WA 98195 USA
关键词
D O I
10.2174/1386207003331454
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Many contemporary applications in computer-aided drug discovery and chemoinformatics depend on representations of molecules by descriptors that capture their structural characteristics and properties. Such applications include, among others, diversity analysis, library design, and virtual screening. Hundreds of molecular descriptors have been reported in the literature, ranging from simple bulk properties to elaborate three-dimensional formulations and complex molecular fingerprints, which sometimes consist of thousands of bit positions. Knowledge-based selection of descriptors that are suitable for specific applications is an important task in chemoinformatics research. If descriptors are to be selected on rational grounds, rather than guesses or chemical intuition, detailed evaluation of their performance is required. A number of studies have been reported that investigate the performance of molecular descriptors in specific applications and/or introduce novel types of descriptors. Progress made in this area is reviewed here in the context of other computational developments in combinatorial chemistry and compound screening.
引用
收藏
页码:363 / 372
页数:10
相关论文
共 71 条
[1]   Designing libraries with CNS activity [J].
Ajay ;
Bemis, GW ;
Murcko, MA .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (24) :4942-4951
[2]  
Antel J, 1999, Curr Opin Drug Discov Devel, V2, P224
[3]  
Apostolakis J, 1999, COMB CHEM HIGH T SCR, V2, P91
[4]   HIGHLY DISCRIMINATING DISTANCE-BASED TOPOLOGICAL INDEX [J].
BALABAN, AT .
CHEMICAL PHYSICS LETTERS, 1982, 89 (05) :399-404
[5]   Binning schemes for partition-based compound selection [J].
Bayley, MJ ;
Willett, P .
JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 1999, 17 (01) :10-18
[6]  
Brown F.K., 1998, Annual Reports in Medicinal Chemistry, V33, P375, DOI 10.1016/s0065-7743(08)61100-8
[7]   Use of structure Activity data to compare structure-based clustering methods and descriptors for use in compound selection [J].
Brown, RD ;
Martin, YC .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1996, 36 (03) :572-584
[8]  
BROWN RD, 1998, J CHEM INF COMP SCI, V38, P983
[9]   Computational methods in molecular diversity and combinatorial chemistry [J].
Bures, MG ;
Martin, YC .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1998, 2 (03) :376-380
[10]   Recursive partitioning analysis of a large structure-activity data set using three-dimensional descriptors [J].
Chen, X ;
Rusinko, A ;
Young, SS .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1998, 38 (06) :1054-1062