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Steps in writing a SMILES code: Break cycles, then write as branches off a main backbone.

The simplified molecular input line entry specification or SMILES is a line notation for the chemical structure of molecules. It uses short series ASCII characters to represent structures. Most molecule editor computer programs can draw a two-dimensional diagram or a three-dimensional model of a molecule based on its SMILES code.

Arthur Weininger and David Weininger wrote the original SMILES specification in the late 1980s. It has since been modified and extended by others, including by Daylight Chemical Information Systems Inc. In 2007, the Blue Obelisk open-source chemistry community developed an open standard called "OpenSMILES".

In July 2006, the International Union of Pure and Applied Chemistry introduced the InChI as a standard line notation for representing chemical structures. People think that it is easier for humans to understand SMILES than InChI. Some chemists argue that SMILES is better than InChI because many different software programs support it. SMILES also has theoretical (for example, graph theory) backing.

Conversion

SMILES can be converted back to 2-dimensional representations using Structure Diagram Generation algorithms.[1] This conversion can sometimes be ambiguous. Because SMILES just says which atoms are connected without any information about the angles between chemical bonds, computer programs use energy minimization to convert SMILES to 3-dimensional representations. There are many downloadable and web-based conversion utilities.

Examples

Here are some examples of the SMILES for molecules:

Molecule Structure SMILES Formula
Dinitrogen N≡N N#N
Methyl isocyanate (MIC) CH3–N=C=O CN=C=O
Copper(II) sulfate Cu2+ SO42- [Cu+2].[O-]S(=O)(=O)[O-]
Œnanthotoxin (C17H22O2) Molecular structure of œnanthotoxin CCC[C@@H](O)CC\C=C\C=C\C#CC#C\C=C\CO
Pyrethrin II (C22H28O5) Molecular structure of pyrethrin II COC(=O)C(\C)=C\C1C(C)(C)[C@H]1C(=O)O[C@@H]2C(C)=C(C(=O)C2)CC=CC=C
Aflatoxin B1 (C17H12O6) Molecular structure of aflatoxin B1 O1C=C[C@H]([C@H]1O2)c3c2cc(OC)c4c3OC(=O)C5=C4CCC(=O)5
Glucose (glucopyranose) (C6H12O6) Molecular structure of glucopyranose OC[C@@H](O1)[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O)1
Bergenin (cuscutin) (a resin) (C14H16O9) Molecular structure of cuscutine (bergenin) OC[C@@H](O1)[C@@H](O)[C@H](O)[C@@H]2[C@@H]1c3c(O)c(OC)c(O)cc3C(=O)O2
A pheromone of the Californian scale insect (3Z,6R)-3-methyl-6-(prop-1-en-2-yl)deca-3,9-dien-1-yl acetate CC(=O)OCCC(/C)=C\C[C@H](C(C)=C)CCC=C
2S,5R-Chalcogran: a pheromone of the bark beetle Pityogenes chalcographus[2] (2S,5R)-2-ethyl-1,6-dioxaspiro[4.4]nonane CC[C@H](O1)CC[C@@]12CCCO2
Vanillin Molecular structure of vanillin O=Cc1ccc(O)c(OC)c1
Melatonin (C13H16N2O2) Molecular structure of melatonin CC(=O)NCCC1=CNc2c1cc(OC)cc2
Flavopereirin (C17H15N2) Molecular structure of flavopereirin CCc(c1)ccc2[n+]1ccc3c2Nc4c3cccc4
Nicotine (C10H14N2) Molecular structure of nicotine CN1CCC[C@H]1c2cccnc2
Alpha-thujone (C10H16O) Molecular structure of thujone CC(C)[C@@]12C[C@@H]1[C@@H](C)C(=O)C2
Thiamin (C12H17N4OS+)
(vitamine B1) 		SMolecular structure of thiamin OCCc1c(C)[n+](=cs1)Cc2cnc(C)nc(N)2

References

  1. ↑ Helson, H.E. (1999). "Structure Diagram Generation". In Lipkowitz, K. B. and Boyd, D. B. (ed.). Rev. Comput. Chem. Reviews in Computational Chemistry. Vol. 13. New York: Wiley-VCH. pp. 313–398. doi:10.1002/9780470125908.ch6. ISBN 9780470125908.((cite book)): CS1 maint: multiple names: editors list (link)
  2. ↑ Isolation of Pheromone Synergists of Bark Bettle, Pityogenes chalcographus, From Complex Insect-Plant Odors by Fractionation and Subtractive-Combination Bioassay

Other websites

Specifications

SMILES related software utilities

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