Literature DB >> 17204261

Re-characterization of three conjugated linolenic acid isomers by GC-MS and NMR.

Ying Cao1, Lin Yang, Hong-Li Gao, Jing-Nan Chen, Zhen-Yu Chen, Qiu-Shi Ren.   

Abstract

Conjugated linolenic acids (CLN) refer to a group of octadecatrienoic acids with three conjugated double bonds. Minor positional and geometrical differences among CLN isomers make their separation and identification difficult. We have used GC-MS and NMR to study three common CLN isomers namely alpha-eleostearic acid, beta-eleostearic acid and punicic acid, finding that some signals of olefinic carbon atoms in NMR spectra were mistakenly assigned in the literature. The present study was therefore undertaken to re-characterize the location of CC double bonds and assign the chemical signals of proton and carbon atoms using (1)H NMR, (13)C NMR, (1)H-(1)H two-dimensional correlation spectra ((1)H-(1)H COSY) and (13)C-(1)H two-dimensional correlation spectra ((13)C-(1)H COSY). The geometrical structure of double bonds in these three CLN isomers was identified using homonuclear decoupling technique.

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Year:  2006        PMID: 17204261     DOI: 10.1016/j.chemphyslip.2006.11.005

Source DB:  PubMed          Journal:  Chem Phys Lipids        ISSN: 0009-3084            Impact factor:   3.329


  2 in total

1.  An ultraviolet spectrophotometric assay for the screening of sn-2-specific lipases using 1,3-O-dioleoyl-2-O-α-eleostearoyl-sn-glycerol as substrate.

Authors:  Lilia D Mendoza; Jorge A Rodriguez; Julien Leclaire; Gerard Buono; Frédéric Fotiadu; Frédéric Carrière; Abdelkarim Abousalham
Journal:  J Lipid Res       Date:  2011-11-23       Impact factor: 5.922

2.  Robust inhibitory effects of conjugated linolenic acids on a cyclooxygenase-related linoleate 10S-dioxygenase: Comparison with COX-1 and COX-2.

Authors:  Zahra Mashhadi; William E Boeglin; Alan R Brash
Journal:  Biochim Biophys Acta       Date:  2015-07-21
  2 in total

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