SAR index: Quantifying the nature of structure - Activity relationships

被引:141
作者
Peltason, Lisa [1 ]
Bajorath, Juergen [1 ]
机构
[1] Univ Bonn, Dept Life Sci Informat, B IT, D-53113 Bonn, Germany
关键词
D O I
10.1021/jm0705713
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Structure-activity relationships (SARs) can display very different features. Small chemical modifications of active molecules often dramatically alter biological responses. By contrast, structurally diverse molecules can have similar activity. SARs can also be heterogeneous in nature. For example, for structurally diverse molecules with similar activity, closely related analogs might have significant differences in potency. Given the inherent complexity of SARs, it has been very difficult to estimate SAR characteristics from molecular structure. On the basis of systematic correlation of 2D structural similarity and compound potency, we have developed a function termed "SAR Index" that quantitatively describes the nature of SARs and establishes different SAR categories: continuous, discontinuous, heterogeneous-relaxed, and heterogeneous-constrained. These heterogeneous SAR categories are described for the first time. Given a set of active compounds and their potency values, SAR Index calculations can estimate how likely it is to identify structurally distinct molecules having similar activity.
引用
收藏
页码:5571 / 5578
页数:8
相关论文
共 13 条
[1]  
[Anonymous], MACCS STRUCTURAL KEY
[2]  
[Anonymous], MOL OP ENV MOE VERS
[3]   Integration of virtual and high-throughput screening [J].
Bajorath, F .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (11) :882-894
[4]   Molecular similarity analysis in virtual screening: foundations, limitations and novel approaches [J].
Eckert, Hanna ;
Bojorath, Juergen .
DRUG DISCOVERY TODAY, 2007, 12 (5-6) :225-233
[5]  
Johnson M., 1990, CONCEPTS APPL MOL SI
[6]   Similarity and dissimilarity: A medicinal chemist's view [J].
Kubinyi, H .
PERSPECTIVES IN DRUG DISCOVERY AND DESIGN, 1998, 9-11 :225-252
[7]   On outliers and activity cliffs - Why QSAR often disappoints [J].
Maggiora, Gerald M. .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2006, 46 (04) :1535-1535
[8]   Molecular similarity analysis uncovers heterogeneous structure-activity relationships and variable activity landscapes [J].
Peltason, Lisa ;
Bajorath, Juergen .
CHEMISTRY & BIOLOGY, 2007, 14 (05) :489-497
[9]  
Shanmugasundaram V., 2001, 222 AM CHEM SOC NATL
[10]   The PDBbind database: Methodologies and updates [J].
Wang, RX ;
Fang, XL ;
Lu, YP ;
Yang, CY ;
Wang, SM .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (12) :4111-4119