Literature DB >> 16562983

Mining a chemical database for fragment co-occurrence: discovery of "chemical clichés".

Eric-Wubbo Lameijer1, Joost N Kok, Thomas Bäck, Ad P Ijzerman.   

Abstract

Nowadays millions of different compounds are known, their structures stored in electronic databases. Analysis of these data could yield valuable insights into the laws of chemistry and the habits of chemists. We have therefore explored the public database of the National Cancer Institute (>250,000 compounds) by pattern searching. We split the molecules of this database into fragments to find out which fragments exist, how frequent they are, and whether the occurrence of one fragment in a molecule is related to the occurrence of another, nonoverlapping fragment. It turns out that some fragments and combinations of fragments are so frequent that they can be called "chemical clichés". We believe that the fragment data can give insight into the chemical space explored so far by synthesis. The lists of fragments and their (co-)occurrences can help create novel chemical compounds by (i) systematically listing the most popular and therefore most easily used substituents and ring systems for synthesizing new compounds, (ii) being an easily accessible repository for rarer fragments suitable for lead compound optimization, and (iii) pointing out some of the yet unexplored parts of chemical space.

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Year:  2006        PMID: 16562983     DOI: 10.1021/ci050370c

Source DB:  PubMed          Journal:  J Chem Inf Model        ISSN: 1549-9596            Impact factor:   4.956


  7 in total

1.  Residue preference mapping of ligand fragments in the Protein Data Bank.

Authors:  Lirong Wang; Zhaojun Xie; Peter Wipf; Xiang-Qun Xie
Journal:  J Chem Inf Model       Date:  2011-03-18       Impact factor: 4.956

2.  Diversification of Nucleophile-Intercepted Beckmann Fragmentation Products and Related Density Functional Theory Studies.

Authors:  Leah L Lowder; Fengyue Zhao; Mathes M Vaughan; K N Houk; Fang Liu; Jimmy Wu
Journal:  J Org Chem       Date:  2020-08-26       Impact factor: 4.354

3.  Scaffold diversity of exemplified medicinal chemistry space.

Authors:  Sarah R Langdon; Nathan Brown; Julian Blagg
Journal:  J Chem Inf Model       Date:  2011-08-31       Impact factor: 4.956

4.  A chemo-centric view of human health and disease.

Authors:  Miquel Duran-Frigola; David Rossell; Patrick Aloy
Journal:  Nat Commun       Date:  2014-12-01       Impact factor: 14.919

5.  Lost in chemical space? Maps to support organometallic catalysis.

Authors:  Natalie Fey
Journal:  Chem Cent J       Date:  2015-06-18       Impact factor: 4.215

6.  Stereoselective construction of sterically hindered oxaspirocycles via chiral bidentate directing group-mediated C(sp3)-O bond formation.

Authors:  Yechan Kim; Seoung-Tae Kim; Dahye Kang; Te-Ik Sohn; Eunyoung Jang; Mu-Hyun Baik; Sungwoo Hong
Journal:  Chem Sci       Date:  2017-11-27       Impact factor: 9.825

7.  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

  7 in total

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