Literature DB >> 9154968

Smart region definition: a new way to improve the predictive ability and interpretability of three-dimensional quantitative structure-activity relationships.

M Pastor1, G Cruciani, S Clementi.   

Abstract

This report describes a new methodology aimed at grouping 3D-QSAR interaction energy descriptors into regions of neighbor variables bearing the same chemical and statistical information. These regions represent the structural variability of the series better than individual descriptor variables and can advantageously replace them in the chemometric analysis. The algorithm used to generate such regions is described, together with their application for improving the quality of GOLPE variable selection. The method is illustrated on a series of 47 glucose analogues, inhibitors of glycogen phosphorylase b, and is shown to improve both the predictive ability and the interpretability of the 3D-QSAR models obtained, comparing favorably with other methods previously described.

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Mesh:

Year:  1997        PMID: 9154968     DOI: 10.1021/jm9608016

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


  14 in total

1.  A comparative molecular field analysis of cytochrome P450 2A5 and 2A6 inhibitors.

Authors:  A Poso; J Gynther; R Juvonen
Journal:  J Comput Aided Mol Des       Date:  2001-03       Impact factor: 3.686

2.  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

3.  An extensive ecdysteroid CoMFA.

Authors:  L Dinan; R E Hormann; T Fujimoto
Journal:  J Comput Aided Mol Des       Date:  1999-03       Impact factor: 3.686

4.  Receptor-based 3D QSAR analysis of estrogen receptor ligands--merging the accuracy of receptor-based alignments with the computational efficiency of ligand-based methods.

Authors:  W Sippl
Journal:  J Comput Aided Mol Des       Date:  2000-08       Impact factor: 3.686

5.  Molecular modelling studies on the ORL1-receptor and ORL1-agonists.

Authors:  Britta M Bröer; Marion Gurrath; Hans-Dieter Höltje
Journal:  J Comput Aided Mol Des       Date:  2003-11       Impact factor: 3.686

6.  Open3DQSAR: a new open-source software aimed at high-throughput chemometric analysis of molecular interaction fields.

Authors:  Paolo Tosco; Thomas Balle
Journal:  J Mol Model       Date:  2010-04-11       Impact factor: 1.810

7.  Autogrid-based clustering of kinases: selection of representative conformations for docking purposes.

Authors:  Giovanni Marzaro; Alessandro Ferrarese; Adriana Chilin
Journal:  Mol Divers       Date:  2014-05-29       Impact factor: 2.943

8.  Development of a unique 3D interaction model of endogenous and synthetic peripheral benzodiazepine receptor ligands.

Authors:  N Cinone; H D Hötje; A Carotti
Journal:  J Comput Aided Mol Des       Date:  2000-11       Impact factor: 3.686

9.  Structure-based 3D QSAR and design of novel acetylcholinesterase inhibitors.

Authors:  W Sippl; J M Contreras; I Parrot; Y M Rival; C G Wermuth
Journal:  J Comput Aided Mol Des       Date:  2001-05       Impact factor: 3.686

10.  3D-QSAR methods on the basis of ligand-receptor complexes. Application of COMBINE and GRID/GOLPE methodologies to a series of CYP1A2 ligands.

Authors:  J J Lozano; M Pastor; G Cruciani; K Gaedt; N B Centeno; F Gago; F Sanz
Journal:  J Comput Aided Mol Des       Date:  2000-05       Impact factor: 3.686

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