Assay Related Target Similarity (ARTS) - Chemogenomics Approach for Quantitative Comparison of Biological Targets

被引:12
作者
Bieler, Michael [1 ]
Heilker, Ralf [1 ]
Koeppen, Herbert [1 ]
Schneider, Gisbert [2 ]
机构
[1] Boehringer Ingelheim Pharma GmbH & Co KG, Lead Identificat & Optimizat Support, D-88397 Biberach, Germany
[2] Swiss Fed Inst Technol, Inst Pharmaceut Sci, CH-8093 Zurich, Switzerland
关键词
PROTEIN-COUPLED-RECEPTORS; LIGAND-BASED APPROACH; SMALL-MOLECULE; ACTIVITY SPECTRA; DRUG DISCOVERY; BINDING-SITES; ANTAGONISTS; PREDICTION; FINGERPRINTS; PHARMACOLOGY;
D O I
10.1021/ci200105t
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Computer-based chemogenomics approaches compare macromolecular drug targets based on their amino acid sequences or derived properties, by similarity of their ligands, or according to ligand-target interaction models. Here we present ARTS (Assay Related Target Similarity) as a quantitative index that estimates target similarity directly from measured affinities of a set of probe compounds. This approach reduces the risk of deducing artificial target relationships from mutually inactive compounds. ARTS implements a scoring scheme that matches intertarget similarity based on dose response measurements. While all experimentally derived target similarities have a tendency to be data set-dependent, we demonstrate that ARTS depends less on the used data set than the commonly used Pearson correlation or Tanimoto index.
引用
收藏
页码:1897 / 1905
页数:9
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