Literature DB >> 18622946

Isolation and structural elucidation of different geometrical isomers of lycopene.

Kati Fröhlich1, Jürgen Conrad, Antje Schmid, Dietmar E Breithaupt, Volker Böhm.   

Abstract

Five geometrical isomers of lycopene were isolated from a photoisomerized mixture on a semi-preparative C30 column and characterized by UV-vis spectroscopy, mass spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy. 1H NMR and 2D NMR measurements were used to unambiguously assign the double bond configuration of five isomers: (5Z,9'Z)-, (9Z)-, (5Z,9Z)-, (all-E)-, and (5Z)-lycopene. This will allow other laboratories to use the results for their C30 HPLC. In addition, it is possible to investigate structure-activity relationships for these lycopene isomers which will improve the understanding of their physiological role in biological tissues.

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Year:  2007        PMID: 18622946     DOI: 10.1024/0300-9831.77.6.369

Source DB:  PubMed          Journal:  Int J Vitam Nutr Res        ISSN: 0300-9831            Impact factor:   1.784


  7 in total

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6.  Enhanced Z-isomerization of tomato lycopene through the optimal combination of food ingredients.

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Journal:  Sci Rep       Date:  2019-05-28       Impact factor: 4.379

7.  Post-Harvest Use of Ultraviolet Light (UV) and Light Emitting Diode (LED) to Enhance Bioactive Compounds in Refrigerated Tomatoes.

Authors:  Nieves Baenas; Celia Iniesta; Rocío González-Barrio; Vanesa Nuñez-Gómez; María Jesús Periago; Francisco Javier García-Alonso
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  7 in total

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