Literature DB >> 25408326

Structure-odor relationships of semisynthetic β-santalol analogs.

Céline Delasalle1, Claire A de March, Uwe J Meierhenrich, Hugues Brevard, Jérôme Golebiowski, Nicolas Baldovini.   

Abstract

A series of eleven β-santalol analogs, including nine new derivatives, was prepared by semisynthesis from natural (-)-(Z)-β-santalol and studied by gas chromatography-olfactometry (GC-O) to characterize their olfactory properties and potencies. These compounds and 45 others selected in the literature were used to build three olfactophores by molecular modelling. Three models were obtained that gather structural and physicochemical constraints that will be useful for further design of new sandalwood odorants.
Copyright © 2014 Verlag Helvetica Chimica Acta AG, Zürich.

Entities:  

Keywords:  Olfactometry; Sandalwood; Structureodor relationship (SOR); β-Santalol

Mesh:

Substances:

Year:  2014        PMID: 25408326     DOI: 10.1002/cbdv.201400082

Source DB:  PubMed          Journal:  Chem Biodivers        ISSN: 1612-1872            Impact factor:   2.408


  2 in total

1.  Chemical features mining provides new descriptive structure-odor relationships.

Authors:  Carmen C Licon; Guillaume Bosc; Mohammed Sabri; Marylou Mantel; Arnaud Fournel; Caroline Bushdid; Jerome Golebiowski; Celine Robardet; Marc Plantevit; Mehdi Kaytoue; Moustafa Bensafi
Journal:  PLoS Comput Biol       Date:  2019-04-25       Impact factor: 4.475

2.  Rationally engineering santalene synthase to readjust the component ratio of sandalwood oil.

Authors:  Wenlong Zha; Fan Zhang; Jiaqi Shao; Xingmei Ma; Jianxun Zhu; Pinghua Sun; Ruibo Wu; Jiachen Zi
Journal:  Nat Commun       Date:  2022-05-06       Impact factor: 17.694

  2 in total

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