Literature DB >> 9385548

Database diversity assessment: new ideas, concepts, and tools.

R Nilakantan1, N Bauman, K S Haraki.   

Abstract

We present some new ideas for characterizing and comparing large chemical databases. The comparison of the contents of large databases is not trivial since it implies pairwise comparison of hundreds of thousands of compounds. We have developed methods for categorizing compounds into groups or series based on their ring-system content, using precalculated structure-based hashcodes. Two large databases can then be compared by simply comparing their hashcode tables. Furthermore, the number of distinct ring-system combinations can be used as an indicator of database diversity. We also present an independent technique for diversity assessment called the saturation diversity approach. This method is based on picking as many mutually dissimilar compounds as possible from a database or a subset thereof. We show that both methods yield similar results. Since the two methods measure very different properties, this probably says more about the properties of the databases studied than about the methods.

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Year:  1997        PMID: 9385548     DOI: 10.1023/a:1007937308615

Source DB:  PubMed          Journal:  J Comput Aided Mol Des        ISSN: 0920-654X            Impact factor:   3.686


  7 in total

1.  Molecular diversity in chemical databases: comparison of medicinal chemistry knowledge bases and databases of commercially available compounds.

Authors:  D J Cummins; C W Andrews; J A Bentley; M Cory
Journal:  J Chem Inf Comput Sci       Date:  1996 Jul-Aug

2.  Stigmata: an algorithm to determine structural commonalities in diverse datasets.

Authors:  N E Shemetulskis; D Weininger; C J Blankley; J J Yang; C Humblet
Journal:  J Chem Inf Comput Sci       Date:  1996 Jul-Aug

3.  The properties of known drugs. 1. Molecular frameworks.

Authors:  G W Bemis; M A Murcko
Journal:  J Med Chem       Date:  1996-07-19       Impact factor: 7.446

4.  Searching for pharmacophores in large coordinate data bases and its use in drug design.

Authors:  R P Sheridan; A Rusinko; R Nilakantan; R Venkataraghavan
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

5.  Measuring diversity: experimental design of combinatorial libraries for drug discovery.

Authors:  E J Martin; J M Blaney; M A Siani; D C Spellmeyer; A K Wong; W H Moos
Journal:  J Med Chem       Date:  1995-04-28       Impact factor: 7.446

6.  Enhancing the diversity of a corporate database using chemical database clustering and analysis.

Authors:  N E Shemetulskis; J B Dunbar; B W Dunbar; D W Moreland; C Humblet
Journal:  J Comput Aided Mol Des       Date:  1995-10       Impact factor: 3.686

7.  Characterising the geometric diversity of functional groups in chemical databases.

Authors:  S M Boyd; M Beverley; L Norskov; R E Hubbard
Journal:  J Comput Aided Mol Des       Date:  1995-10       Impact factor: 3.686

  7 in total
  6 in total

Review 1.  An overview of the diversity represented in commercially-available databases.

Authors:  Mary P Bradley
Journal:  J Comput Aided Mol Des       Date:  2002 May-Jun       Impact factor: 3.686

Review 2.  An overview of the diversity represented in commercially-available databases.

Authors:  Mary P Bradley
Journal:  Mol Divers       Date:  2002       Impact factor: 2.943

3.  An enriched structural kinase database to enable kinome-wide structure-based analyses and drug discovery.

Authors:  Natasja Brooijmans; Yu-Wei Chang; Dominick Mobilio; Rajiah A Denny; Christine Humblet
Journal:  Protein Sci       Date:  2010-04       Impact factor: 6.725

4.  GPU accelerated chemical similarity calculation for compound library comparison.

Authors:  Chao Ma; Lirong Wang; Xiang-Qun Xie
Journal:  J Chem Inf Model       Date:  2011-07-01       Impact factor: 4.956

5.  Lessons learnt from assembling screening libraries for drug discovery for neglected diseases.

Authors:  Ruth Brenk; Alessandro Schipani; Daniel James; Agata Krasowski; Ian Hugh Gilbert; Julie Frearson; Paul Graham Wyatt
Journal:  ChemMedChem       Date:  2008-03       Impact factor: 3.466

6.  Synthesis of natural-product-like molecules with over eighty distinct scaffolds.

Authors:  Daniel Morton; Stuart Leach; Christopher Cordier; Stuart Warriner; Adam Nelson
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

  6 in total

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