Literature DB >> 1448432

A quantitative structure-activity relationship (QSAR) study of alkylpyrazine odor modalities.

A Tsantili-Kakoulidou1, L B Kier.   

Abstract

The odor strength of a series of alkylpyrazines has been quantitatively investigated applying molecular connectivity, molecular shape, and the recently developed electrotopological state indices. The successful use of the latter parameters indicates that both electronic and topological features contribute to the odor strength of the compounds under study, while the specific role of the two nitrogen atoms is revealed.

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Year:  1992        PMID: 1448432     DOI: 10.1023/a:1015865603263

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  3 in total

1.  An electrotopological-state index for atoms in molecules.

Authors:  L B Kier; L H Hall
Journal:  Pharm Res       Date:  1990-08       Impact factor: 4.200

2.  Odor quality and chemical structure in fruit and vegetable flavors.

Authors:  R Teranishi; R G Buttery; D G Guadagni
Journal:  Ann N Y Acad Sci       Date:  1974-09-27       Impact factor: 5.691

3.  Specific anosmia: a clue to the olfactory code.

Authors:  J E Amoore
Journal:  Nature       Date:  1967-06-10       Impact factor: 49.962

  3 in total
  3 in total

1.  E-state fields: applications to 3D QSAR.

Authors:  G E Kellogg; L B Kier; P Gaillard; L H Hall
Journal:  J Comput Aided Mol Des       Date:  1996-12       Impact factor: 3.686

2.  Predicting olfactory receptor neuron responses from odorant structure.

Authors:  Michael Schmuker; Marien de Bruyne; Melanie Hähnel; Gisbert Schneider
Journal:  Chem Cent J       Date:  2007-05-04       Impact factor: 4.215

Review 3.  The scent of wolves: pyrazine analogs induce avoidance and vigilance behaviors in prey.

Authors:  Kazumi Osada; Sadaharu Miyazono; Makoto Kashiwayanagi
Journal:  Front Neurosci       Date:  2015-10-07       Impact factor: 4.677

  3 in total

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