<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Grougnet, R.a</style></author><author><style face="normal" font="default" size="100%">Magiatis, P.b</style></author><author><style face="normal" font="default" size="100%">Laborie, H.b</style></author><author><style face="normal" font="default" size="100%">Lazarou, D.c</style></author><author><style face="normal" font="default" size="100%">Papadopoulos, A.c</style></author><author><style face="normal" font="default" size="100%">Skaltsounis, A.-L.b</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Sesamolinol glucoside, disaminyl ether, and other lignans from sesame seeds</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Agricultural and Food Chemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Adsorption</style></keyword><keyword><style  face="normal" font="default" size="100%">Antimutagenic activity</style></keyword><keyword><style  face="normal" font="default" size="100%">article</style></keyword><keyword><style  face="normal" font="default" size="100%">Benzo[a]pyrene</style></keyword><keyword><style  face="normal" font="default" size="100%">chemistry</style></keyword><keyword><style  face="normal" font="default" size="100%">Ethers</style></keyword><keyword><style  face="normal" font="default" size="100%">glucoside</style></keyword><keyword><style  face="normal" font="default" size="100%">Glucosides</style></keyword><keyword><style  face="normal" font="default" size="100%">Heteronuclear</style></keyword><keyword><style  face="normal" font="default" size="100%">Isolated compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">lignan</style></keyword><keyword><style  face="normal" font="default" size="100%">lignans</style></keyword><keyword><style  face="normal" font="default" size="100%">mass spectrometry</style></keyword><keyword><style  face="normal" font="default" size="100%">Mass spectroscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">Multiple-quantum coherences</style></keyword><keyword><style  face="normal" font="default" size="100%">Natural compounds</style></keyword><keyword><style  face="normal" font="default" size="100%">Nuclear magnetic resonance</style></keyword><keyword><style  face="normal" font="default" size="100%">Nuclear magnetic resonance spectroscopy</style></keyword><keyword><style  face="normal" font="default" size="100%">Nuclear magnetic resonance techniques</style></keyword><keyword><style  face="normal" font="default" size="100%">Nuclear overhauser effect spectrometries</style></keyword><keyword><style  face="normal" font="default" size="100%">plant extract</style></keyword><keyword><style  face="normal" font="default" size="100%">Plant Extracts</style></keyword><keyword><style  face="normal" font="default" size="100%">plant seed</style></keyword><keyword><style  face="normal" font="default" size="100%">Quantum theory</style></keyword><keyword><style  face="normal" font="default" size="100%">Resins</style></keyword><keyword><style  face="normal" font="default" size="100%">Seeds</style></keyword><keyword><style  face="normal" font="default" size="100%">sesamolinol diglucoside</style></keyword><keyword><style  face="normal" font="default" size="100%">Sesamum</style></keyword><keyword><style  face="normal" font="default" size="100%">Sesamum indicum</style></keyword><keyword><style  face="normal" font="default" size="100%">Spectroscopic analysis</style></keyword><keyword><style  face="normal" font="default" size="100%">Spectroscopic method</style></keyword><keyword><style  face="normal" font="default" size="100%">XAD-4 resin adsorption</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2012</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://www.scopus.com/inward/record.url?eid=2-s2.0-84855805423&amp;partnerID=40&amp;md5=877004b678b633c1071f7fbf6aa136e3</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">1</style></number><volume><style face="normal" font="default" size="100%">60</style></volume><pages><style face="normal" font="default" size="100%">108-111</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The application of a procedure based on XAD-4 adsorption resin permitted the obtainment of an enriched polyphenolic extract from Sesamum indicum seeds. Chemical analysis of the obtained extract led to the identification of 12 lignans. Among them, 2 lignans, (+)-sesamolinol-4'-O-β-d-glucoside and disaminyl ether, are reported for the first time as natural compounds. Their structure has been determined by spectroscopic methods, mainly by the application of one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance (NMR) techniques [heteronuclear multiple-quantum coherence (HMQC), heteronuclear multiple-bond correlation (HMBC), and nuclear Overhauser effect spectrometry (NOESY)] and mass spectroscopy. The isolated compounds were evaluated for their antimutagenic activity. Among the tested lignans, the most active lignan was found to be sesamolin, followed by sesamolinol and samin, against H2O2. Additionally, some of the tested lignans showed desmutagenic activity against benzo[a]pyrene (BaP). © 2011 American Chemical Society.</style></abstract><notes><style face="normal" font="default" size="100%">cited By (since 1996)2</style></notes></record></records></xml>