Literature DB >> 17636943

Algorithm for advanced canonical coding of planar chemical structures that considers stereochemical and symmetric information.

Shungo Koichi1, Satoru Iwata, Takeaki Uno, Hiroyuki Koshino, Hiroko Satoh.   

Abstract

We describe a rigorous and fast algorithm for advanced canonical coding of planar chemical structures based on the algorithm of Faulon et al. (J. Chem. Inf. Comput. Sci. 2004, 44, 427-436). Our algorithm works well even for highly symmetric structures; moreover, an advantage of our algorithm includes providing a rigorous canonical numbering of atoms with a consideration of stereochemistry and recognizing symmetric moieties. The planar structural line notation with the canonical numbering is also fit for use with stereochemical line notation. These capabilities are usable for general purposes in chemical structural coding and are particularly essential for detecting equivalent atoms in NMR studies. This algorithm was implemented on a 13C NMR chemical shift prediction system CAST/CNMR. Applications of the algorithm to several organic compounds demonstrate the practical efficiency of the rigorous coding.

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Year:  2007        PMID: 17636943     DOI: 10.1021/ci600238j

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


  3 in total

1.  Towards a Universal SMILES representation - A standard method to generate canonical SMILES based on the InChI.

Authors:  Noel M O'Boyle
Journal:  J Cheminform       Date:  2012-09-18       Impact factor: 5.514

2.  Atomic ring invariant and Modified CANON extended connectivity algorithm for symmetry perception in molecular graphs and rigorous canonicalization of SMILES.

Authors:  Dmytro G Krotko
Journal:  J Cheminform       Date:  2020-08-20       Impact factor: 5.514

Review 3.  Artificial Intelligence for Autonomous Molecular Design: A Perspective.

Authors:  Rajendra P Joshi; Neeraj Kumar
Journal:  Molecules       Date:  2021-11-09       Impact factor: 4.411

  3 in total

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