Literature DB >> 18038162

Effect of steric molecular field settings on CoMFA predictivity.

Ruchi R Mittal1, Ross A McKinnon, Michael J Sorich.   

Abstract

Steric molecular field can be represented in a number of ways in comparative molecular field analysis (CoMFA). This study aimed to investigate whether the choice of steric molecular field settings significantly influences the predictive performance of CoMFA and, if so, which is the best. The three-dimensional quantitative structure activity relationship (3D-QSAR) models based on Lennard-Jones, indicator, parabolic and Gaussian steric fields were compared using 28 datasets taken from the literature. The analysis of the predictive ability of these models (cross validated R(2)) indicates that steric fields in which the value drops off quickly with distance (i.e. Lennard-Jones and indicator fields) tend to perform better than the Gaussian version, which has a slower and smoother decrease. Furthermore, depending on the steric field type used, the field sampling density (i.e. grid spacing) has a variable influence on the predictive ability of the models generated.

Mesh:

Year:  2007        PMID: 18038162     DOI: 10.1007/s00894-007-0252-1

Source DB:  PubMed          Journal:  J Mol Model        ISSN: 0948-5023            Impact factor:   1.810


  28 in total

1.  3D-QSAR CoMFA on cyclin-dependent kinase inhibitors.

Authors:  P Ducrot; M Legraverend; D S Grierson
Journal:  J Med Chem       Date:  2000-11-02       Impact factor: 7.446

2.  Three-dimensional quantitative structure-activity relationship studies on selected MT1 and MT2 melatonin receptor ligands: requirements for subtype selectivity and intrinsic activity modulation.

Authors:  Silvia Rivara; Marco Mor; Claudia Silva; Valentina Zuliani; Federica Vacondio; Gilberto Spadoni; Annalida Bedini; Giorgio Tarzia; Valeria Lucini; Marilou Pannacci; Franco Fraschini; Pier Vincenzo Plazzi
Journal:  J Med Chem       Date:  2003-04-10       Impact factor: 7.446

3.  3D-QSAR study of ring-substituted quinoline class of anti-tuberculosis agents.

Authors:  Amit Nayyar; Alpeshkumar Malde; Rahul Jain; Evans Coutinho
Journal:  Bioorg Med Chem       Date:  2005-10-07       Impact factor: 3.641

4.  Variable selection and interpretation in structure-affinity correlation modeling of estrogen receptor binders.

Authors:  Federico Marini; Alessandra Roncaglioni; Marjana Novic
Journal:  J Chem Inf Model       Date:  2005 Nov-Dec       Impact factor: 4.956

5.  Exploring phase-transfer catalysis with molecular dynamics and 3D/4D quantitative structure-selectivity relationships.

Authors:  James L Melville; Kevin R J Lovelock; Claire Wilson; Bryan Allbutt; Edmund K Burke; Barry Lygo; Jonathan D Hirst
Journal:  J Chem Inf Model       Date:  2005 Jul-Aug       Impact factor: 4.956

6.  A 3D QSAR CoMFA study of non-peptide angiotensin II receptor antagonists.

Authors:  L Belvisi; G Bravi; G Catalano; M Mabilia; A Salimbeni; C Scolastico
Journal:  J Comput Aided Mol Des       Date:  1996-12       Impact factor: 3.686

7.  Molecular similarity indices in a comparative analysis (CoMSIA) of drug molecules to correlate and predict their biological activity.

Authors:  G Klebe; U Abraham; T Mietzner
Journal:  J Med Chem       Date:  1994-11-25       Impact factor: 7.446

8.  Structural determinants of high-affinity binding of ryanoids to the vertebrate skeletal muscle ryanodine receptor: a comparative molecular field analysis.

Authors:  W Welch; S Ahmad; J A Airey; K Gerzon; R A Humerickhouse; H R Besch; L Ruest; P Deslongchamps; J L Sutko
Journal:  Biochemistry       Date:  1994-05-24       Impact factor: 3.162

9.  A 3D QSAR study on a set of dopamine D4 receptor antagonists.

Authors:  Jonas Boström; Markus Böhm; Klaus Gundertofte; Gerhard Klebe
Journal:  J Chem Inf Comput Sci       Date:  2003 May-Jun

10.  Comparing the quality and predictiveness between 3D QSAR models obtained from manual and automated alignment.

Authors:  Anu J Tervo; Tommi H Nyrönen; Toni Rönkkö; Antti Poso
Journal:  J Chem Inf Comput Sci       Date:  2004 May-Jun
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  1 in total

1.  Molecular docking and 3D-quantitative structure activity relationship analyses of peptidyl vinyl sulfones: Plasmodium Falciparum cysteine proteases inhibitors.

Authors:  Cátia Teixeira; José R B Gomes; Thierry Couesnon; Paula Gomes
Journal:  J Comput Aided Mol Des       Date:  2011-07-24       Impact factor: 3.686

  1 in total

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