Literature DB >> 7783140

Receptor surface models. 2. Application to quantitative structure-activity relationships studies.

M Hahn1, D Rogers.   

Abstract

A new technique for using receptor surface models in quantitative structure-activity relationship (QSAR) analysis is described. Receptor surface models provide compact, quantitative descriptors which capture three-dimensional information about putative receptor/ligand interactions. Receptor surface models can be constructed quickly, which allows the construction of multiple plausible models; a variable selection technique such as genetic function approximation (GFA) can then be used to suggest which receptor surface models provide the most valuable descriptors for QSAR. Advantages of this approach are shown by applying it against two previously-published and well-studied QSAR data sets. Our results indicate that the approach can model data as effectively as established 3D-QSAR techniques.

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Year:  1995        PMID: 7783140     DOI: 10.1021/jm00012a008

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  12 in total

1.  FILO (field interaction ligand optimization): a simplex strategy for searching the optimal ligand interaction field in drug design.

Authors:  F Melani; P Gratteri; M Adamo; C Bonaccini
Journal:  J Comput Aided Mol Des       Date:  2001-01       Impact factor: 3.686

2.  Evaluation of a novel molecular vibration-based descriptor (EVA) for QSAR studies: 2. Model validation using a benchmark steroid dataset.

Authors:  D B Turner; P Willett; A M Ferguson; T W Heritage
Journal:  J Comput Aided Mol Des       Date:  1999-05       Impact factor: 3.686

3.  A comparative study of ligand-receptor complex binding affinity prediction methods based on glycogen phosphorylase inhibitors.

Authors:  S S So; M Karplus
Journal:  J Comput Aided Mol Des       Date:  1999-05       Impact factor: 3.686

4.  Evaluation of designed ligands by a multiple screening method: application to glycogen phosphorylase inhibitors constructed with a variety of approaches.

Authors:  S S So; M Karplus
Journal:  J Comput Aided Mol Des       Date:  2001-07       Impact factor: 3.686

5.  A comparative docking study and the design of potentially selective MMP inhibitors.

Authors:  S Hanessian; N Moitessier; E Therrien
Journal:  J Comput Aided Mol Des       Date:  2001-10       Impact factor: 3.686

6.  Internally defined distances in 3D-quantitative structure-activity relationships.

Authors:  Christian Th Klein; Norbert Kaiblinger; Peter Wolschann
Journal:  J Comput Aided Mol Des       Date:  2002-02       Impact factor: 3.686

Review 7.  Comparative molecular surface analysis: a novel tool for drug design and molecular diversity studies.

Authors:  Jaroslaw Polanski; Rafal Gieleciak
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

8.  Evaluation of a novel infrared range vibration-based descriptor (EVA) for QSAR studies. 1. General application.

Authors:  D B Turner; P Willett; A M Ferguson; T Heritage
Journal:  J Comput Aided Mol Des       Date:  1997-07       Impact factor: 3.686

Review 9.  Evolutionary algorithms in computer-aided molecular design.

Authors:  D E Clark; D R Westhead
Journal:  J Comput Aided Mol Des       Date:  1996-08       Impact factor: 3.686

10.  Objective models for steroid binding sites of human globulins.

Authors:  J Schnitker; R Gopalaswamy; G M Crippen
Journal:  J Comput Aided Mol Des       Date:  1997-01       Impact factor: 3.686

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