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1. Full Text Enterolignan-producing phenotypes are associated with increased gut microbial diversity and altered composition in premenopausal women in the United States
by Hullar, Meredith A.J and Lancaster, Samuel M and Li, Fei and Tseng, Elizabeth and Beer, Karlyn and Atkinson, Charlotte and Wähälä, Kristiina and Copeland, Wade K and Randolph, Timothy W and Newton, Katherine M and Lampe, Johanna W
Cancer Epidemiology Biomarkers and Prevention, ISSN 1055-9965, 03/2015, Volume 24, Issue 3, pp. 546 - 554
Background: Lignans in plant foods are metabolized by gut bacteria to the enterolignans, enterodiol (END) and enterolactone (ENL). Enterolignans have biologic... 
KOREAN NATIVE CATTLE | MAMMALIAN LIGNANS | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | ONCOLOGY | BREAST-CANCER RISK | SECOISOLARICIRESINOL DIGLUCOSIDE | DIETARY LIGNANS | NATIONAL-HEALTH | SP-NOV | URINARY LIGNANS | HUMAN INTESTINAL BACTERIA | PLANT LIGNANS | United States | Humans | Middle Aged | Diet Records | Gastrointestinal Tract - microbiology | Lignans - biosynthesis | Lignans - metabolism | Gastrointestinal Tract - metabolism | 4-Butyrolactone - metabolism | Microbiota | Phenotype | Adult | Female | 4-Butyrolactone - analogs & derivatives | Premenopause - metabolism | lignan | diversity | gut microbiome | phytochemical
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2. Full Text Absorption of plant lignans from cereals in an experimental pig model
by Bolvig, Anne Katrine and Adlercreutz, Herman and Theil, Peter Kappel and Jorgensen, Henry and Knudsen, Knud Erik Bach
British Journal of Nutrition, ISSN 0007-1145, 05/2016, Volume 115, Issue 10, pp. 1711 - 1720
Plant lignans are diphenolic compounds ingested with whole grains and seeds and converted to enterolignans by the colonic microbiota. In the present study, we... 
Plasma | Absorption of lignans | Cereals | Catheterised pigs | Lignans | WHOLE-WHEAT GRAIN | QUANTITATIVE ASPECTS | SERUM ENTEROLACTONE | PLASMA ENTEROLACTONE | BINDING GLOBULIN SHBG | SECOISOLARICIRESINOL-DIGLYCOSIDE | MAMMALIAN LIGNANS | IN-VITRO | NUTRITION & DIETETICS | LIQUID-CHROMATOGRAPHY | RYE INGREDIENTS | Secale - chemistry | Lignans - blood | Lignans - urine | Bread | Lignans - administration & dosage | Flour - analysis | Lignans - pharmacokinetics | Animals | Swine | Female | Models, Animal | Intestine, Small - metabolism | Triticum - chemistry | Edible Grain - chemistry | Diet - veterinary | Lignin | Diet | Nutrition | Grain
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3. Full Text Lignans of sesame: Purification methods, biological activities and biosynthesis – A review
by Dar, Aejaz Ahmad and Arumugam, Neelakantan
Bioorganic Chemistry, ISSN 0045-2068, 10/2013, Volume 50, pp. 1 - 10
Lignans are a group of compounds consisting of dimers of phenyl propane units. They are found in diverse forms distributed in a variety of plants. Sesame... 
Sesamum indicum | Sesamin | Enterolignans | Biosynthesis | HPLC | Lignans | SECONDARY METABOLITES | OXIDATIVE STRESS | INDICUM L. SEEDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | BREAST-CANCER | MAMMALIAN LIGNANS | FUROFURAN LIGNAN | CHEMICAL-CONSTITUENTS | SERUM ENTEROLACTONE CONCENTRATION | MOLT 4B CELLS | BRAZILIAN MYRISTICACEAE | Diet | Lignans - chemistry | Humans | Lignans - biosynthesis | Molecular Structure | Sesamum - chemistry | Lignans - isolation & purification
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4. Full Text Recent advances in research on lignans and neolignans
by Teponno, Rémy Bertrand and Kusari, Souvik and Spiteller, Michael
Natural Product Reports, ISSN 0265-0568, 8/2016, Volume 33, Issue 9, pp. 144 - 192
Covering: 2009 to 2015 Lignans and neolignans are a large group of natural products derived from the oxidative coupling of two C6-C3 units. Owing to their... 
BIOACTIVE LIGNANS | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | INHIBITORY-ACTIVITY | CHEMISTRY, ORGANIC | DIBENZOCYCLOOCTADIENE LIGNANS | NITRIC-OXIDE PRODUCTION | SCHIZANDRA-CHINENSIS BAILL | AERIAL PARTS | SCHISANDRA-SPHENANTHERA | SAURURUS-CHINENSIS | ANTIINFLAMMATORY ACTIVITIES | PHENOLIC GLYCOSIDES | Antiviral Agents - pharmacology | Antioxidants - chemistry | Anti-Inflammatory Agents - pharmacology | Lignans - chemistry | Humans | Biological Products - pharmacology | Glycosides - pharmacology | Lignans - pharmacology | Biological Products - isolation & purification | HIV - drug effects | Biological Products - chemistry | Anti-Inflammatory Agents - chemistry | Antiviral Agents - chemistry | Molecular Structure | Glycosides - chemistry
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5. Full Text Modular synthesis and biological investigation of 5-hydroxymethyl dibenzyl butyrolactones and related lignans
by Davidson, Samuel J and Pilkington, Lisa I and Dempsey-Hibbert, Nina C and El-Mohtadi, Mohamed and Tang, Shiying and Wainwright, Thomas and Whitehead, Kathryn A and Barker, David
Molecules, ISSN 1420-3049, 11/2018, Volume 23, Issue 12, p. 3057
Dibenzyl butyrolactone lignans are well known for their excellent biological properties, particularly for their notable anti-proliferative activities. Herein... 
Acyl-Claisen | Anti-proliferative | Dibenzyl butyrolactones | Stereoselective synthesis | Lignans | DIBENZYLBUTYROLACTONE LIGNANS | ARCTIUM-LAPPA | dibenzyl butyrolactones | ASYMMETRIC-SYNTHESIS | ENANTIOSELECTIVE SYNTHESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL-CYCLE ARREST | CYTOTOXIC ACTIVITY | CHEMISTRY, MULTIDISCIPLINARY | lignans | anti-proliferative | GAMMA-BUTYROLACTONES | NATURAL LIGNANS | acyl-Claisen | stereoselective synthesis | ACYL-CLAISEN APPROACH | DERIVATIVES | Cell Survival - drug effects | Jurkat Cells | Lignans - chemistry | Stereoisomerism | Furans - pharmacology | Humans | Lignans - pharmacology | Lactones - pharmacology | Lactones - chemical synthesis | Furans - chemistry | Lignans - chemical synthesis | Molecular Structure | 4-Butyrolactone - analogs & derivatives | Furans - chemical synthesis | Lactones - chemistry
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6. Full Text Profiling and identification of the absorbed constituents and metabolites of schisandra lignans by ultra‐performance liquid chromatography coupled to mass spectrometry
by Sun, Hui and Wu, Fangfang and Zhang, Aihua and Wei, Wenfeng and Han, Ying and Wang, Xijun
Biomedical Chromatography, ISSN 0269-3879, 11/2013, Volume 27, Issue 11, pp. 1511 - 1519
Schisandra chinensis Baill grows wild in Russia, China, Korea and Japan, and its fruit has been found to be effective in amnesia and insomnia. It is enriched... 
Schisandra | biotransformation | mass spectrometry | metabolism | Metabolynx | lignans | ultra‐performance liquid chromatography | Schisandra lignans | Metabolism | Mass spectrometry | Biotransformation | Ultra-performance liquid chromatography | STEMONAE | FRUITS | CHEMISTRY, ANALYTICAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | MS/MS | SHENGMAI SAN | CHINENSIS TURCZ | DIBENZOCYCLOOCTADIENE LIGNANS | RHEIN | EXTRACTION | PHARMACOKINETICS | ultra-performance liquid chromatography | PHARMACOLOGY & PHARMACY | RAT PLASMA | Chromatography, High Pressure Liquid - methods | Hydroxylation | Rats, Wistar | Schisandra - metabolism | Administration, Oral | Lignans - blood | Schisandra - chemistry | Plant Extracts - blood | Rats | Male | Lignans - metabolism | Lignans - administration & dosage | Plant Extracts - administration & dosage | Plant Extracts - analysis | Plant Extracts - metabolism | Animals | Spectrometry, Mass, Electrospray Ionization - methods | Methylation | Lignans - analysis | Liquid chromatography | Metabolites | Analysis
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7. Dibenzylbutyrolactone lignans – a review of their structural diversity, biosynthesis, occurrence, identification and importance
by Sólyomváry, Anna and Béni, Szabolcs and Boldizsár, Imre
Mini-Reviews in Medicinal Chemistry, ISSN 1389-5575, 2016, Volume 16, Issue 12, pp. 1053 - 1074
Objective: Dibenzylbutyrolactone lignans represent a unique group of plant secondary metabolites with increasing significance in medicine. This review... 
Arctigenin | Analysis | Chemotaxonomy | Lignan | Biosynthesis | Dibenzylbutyrolactone | Biological activity | SECONDARY METABOLITES | CHEMISTRY, MEDICINAL | biological activity | PODOPHYLLOTOXIN RELATED LIGNANS | dibenzylbutyrolactone | STEM BARK | CYTOTOXIC LIGNANS | CELL-CYCLE ARREST | chemotaxonomy | SESQUITERPENE LACTONES | arctigenin | lignan | IN-VITRO | CHEMICAL-CONSTITUENTS | AERIAL PARTS | biosynthesis | THUJA-PLICATA | Cell Survival - drug effects | Antiviral Agents - pharmacology | Furans - metabolism | Lignans - chemistry | Humans | Anticonvulsants - metabolism | Lignans - biosynthesis | Antiviral Agents - metabolism | Antineoplastic Agents - chemistry | Anticonvulsants - pharmacology | Lignans - pharmacology | Antineoplastic Agents - toxicity | Antineoplastic Agents - metabolism | Lignans - pharmacokinetics | Plants - metabolism | Signal Transduction - drug effects | Antiviral Agents - chemistry | Coronavirus - drug effects | Furans - chemistry | Anticonvulsants - chemistry | Plants - chemistry
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8. Full Text Meta-analyses of lignans and enterolignans in relation to breast cancer risk
by Buck, Katharina and Zaineddin, Aida Karina and Vrieling, Alina and Linseisen, Jakob and Chang-Claude, Jenny
American Journal of Clinical Nutrition, ISSN 0002-9165, 07/2010, Volume 92, Issue 1, pp. 141 - 153
Background: Epidemiologic studies that examined whether lignans, the most important class of phytoestrogens in the Western diet, protect against breast cancer... 
MAMMALIAN LIGNANS | NUTRITION & DIETETICS | CLINICAL-TRIALS | DIETARY PHYTOESTROGEN INTAKE | FLAVONOID INTAKE | PHYTO-ESTROGENS | ESTROGEN-RECEPTOR STATUS | PLASMA ENTEROLACTONE | POSTMENOPAUSAL WOMEN | SERUM ENTEROLACTONE CONCENTRATION | CYP17 GENOTYPE | Premenopause | Lignans - blood | Humans | Risk Factors | Lignans - urine | Lignans - pharmacology | Case-Control Studies | Breast Neoplasms - prevention & control | Pregnancy | Lignans - pharmacokinetics | Postmenopause | Female | Parity | Breast Neoplasms - epidemiology | Cohort Studies | Prevention | Breast cancer | Research | Health aspects | Risk factors | Isoflavones
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9. Full Text A strategy for preparative separation of 10 lignans from justicia procumbens L. by high-speed counter-current chromatography
by Jiang, Jiaojiao and Dong, Hongjing and Wang, Tao and Zhao, Ruixuan and Mu, Yan and Geng, Yanling and Zheng, Zhenjia and Wang, Xiao
Molecules, ISSN 1420-3049, 12/2017, Volume 22, Issue 12, p. 2024
Ten compounds, including three lignan glycosides and seven lignans, were purified from Justicia procumbens L. in 8 h using an efficient strategy based on... 
Justicia procumbens L | Preparative separation | High-speed counter-current chromatography | Lignans and their glycosides | preparative separation | COMPLETE ASSIGNMENTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CYTOTOXIC LIGNANS | C-13 NMR DATA | H-1 | CHEMISTRY, MULTIDISCIPLINARY | PURIFICATION | high-speed counter-current chromatography | lignans and their glycosides | ARYLNAPHTHALIDE LIGNANS | ALKALOIDS | Solvents | Justicia - chemistry | Spectrometry, Mass, Electrospray Ionization | Magnetic Resonance Spectroscopy | Lignans - chemistry | Molecular Structure | Chromatography, High Pressure Liquid | Lignans - isolation & purification | Separation | Nuclear magnetic resonance--NMR | Methyl alcohol | Lignans | High speed | Glycosides | Strategy | Ethyl acetate | Acetic acid | Petroleum | Chromatography | Methanol
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10. Full Text Identification of metabolites of deoxyschizandrin in rats by UPLC–Q-TOF-MS/MS based on multiple mass defect filter data acquisition and multiple data processing techniques
by Liu, Minyan and Liu, Ting and Zhao, Shaohua and Wang, Cuicui and Wang, Hongtao and Wang, Zongquan and Wang, Yufeng and Li, Song and Tu, Pengfei
Journal of Chromatography B, ISSN 1570-0232, 02/2014, Volume 949-950, pp. 115 - 126
Deoxyschizandrin is an active lignin ingredient originating from or . In the present study, a novel and efficient strategy was developed for the screening and... 
Deoxyschizandrin | Multiple mass defect filter | Identification | Multiple data processing | Metabolites | UPLC–Q-TOF-MS/MS | UPLC-Q-TOF-MS/MS | CHEMISTRY, ANALYTICAL | PROFILES | CHINENSIS | BIOCHEMICAL RESEARCH METHODS | PLASMA | SCHISANDRA-SPHENANTHERA | LIGNANS | URINARY METABOLITES | SPECTROMETRY | EXTRACT | Polycyclic Compounds - chemistry | Chromatography, High Pressure Liquid - methods | Oxidation-Reduction | Lignans - chemistry | Bile - chemistry | Models, Molecular | Rats | Cyclooctanes - metabolism | Lignans - urine | Male | Lignans - metabolism | Polycyclic Compounds - analysis | Rats, Sprague-Dawley | Cyclooctanes - analysis | Animals | Cyclooctanes - urine | Metabolic Networks and Pathways | Cyclooctanes - chemistry | Tandem Mass Spectrometry - methods | Lignans - analysis | Polycyclic Compounds - metabolism | Polycyclic Compounds - urine | Filtration | Filtering | Biocompatibility | Data processing | Strategy | Defects
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11. Full Text Lignans
by Barker, David
2019, ISBN 9783038979081
Lignans are a class of natural products found mainly in plants. They have a wide variety of structures and exhibit a range of potent biological activities.... 
antibacterial activity | semisynthesis | dibenzyl butyrolactones | flavonoid glycoside | taste-active compound | lignan glycoside | heilaohu | chemical characterization | 9-norlignans | antioxidant activity | drug-like | human health | hydroxymatairesinol | podophyllotoxin | chemometrics | lignan | bitterness | Lespedeza cuneata | red-flowered Chinese magnolia vine | Bursera | antioxidant | ruminant | secoisolariciresinol diglucoside | quantification | oak ageing | intermolecular interactions | cattle | Schisandrae Chinensis Fructus | anti-inflammatory activity | acyl-Claisen | F-actin | cultivar | UHPLC-MS/MS | LOX | bioactivity | podophyllotoxin-type lignans | harmonized databases | seed | graph theory | antioxidants | food groups | health promotion | microtubules | anti-proliferative | simultaneous quantitation | acetylcholinesterase inhibitors | natural products | flax | arylnaphthalene lignan | epiboly | dietary intake | aryldihydronaphthalene lignan | multiple bioactive components | enterolignan | cell migration | chemical space | total synthesis | diet | Lauraceae | pharmacokinetic | cytotoxicity | tujia ethnomedicine | genetic | synthesis | cultivated | flavonolignans | cell cycle | chronic diseases | flavonol | national databases | oxidation | chemical components | adipocyte and osteoblast differentiation | Burseraceae | molecular dynamics | COX | lignans | hydroxycinnamic acid | chemical structures | environment | dietary lignans | phytochemical analysis | Schisandra chinensis | Chinese magnolia vine | animal health | neolignans | stereoselective synthesis | Schisandra rubriflora | sPLA2 | cancer | Bursera fagaroides | norlignans | in silico studies | wild
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12. Full Text Gardenifolins A-H, Scalemic Neolignans from Gardenia ternifolia: Chiral Resolution, Configurational Assignment, and Cytotoxic Activities against the HeLa Cancer Cell Line
by Tshitenge, Dieudonné Tshitenge and Feineis, Doris and Awale, Suresh and Bringmann, Gerhard
Journal of Natural Products, ISSN 0163-3864, 05/2017, Volume 80, Issue 5, pp. 1604 - 1614
From the tropical plant Gardenia ternifolia Schumach. and Thonn. (Rubiaceae), eight stereoisomeric 2,3-dihydrobenzo[b]furan neolignans, named gardenifolins A H... 
CHEMISTRY, MEDICINAL | ENANTIOMERIC LIGNANS | ANTHOCYANINS | ANTIOXIDANT LIGNANS | ACORUS-TATARINOWII | SANTALUM-ALBUM | PLANT SCIENCES | ABSOLUTE-CONFIGURATION | SELAGINELLA-MOELLENDORFFII | INSERTION REACTION | CRATAEGUS-PINNATIFIDA | PHARMACOLOGY & PHARMACY | XANTHIUM-SIBIRICUM | Magnetic Resonance Spectroscopy | Apoptosis - drug effects | Lignans - chemistry | Stereoisomerism | Humans | Crystallography, X-Ray | Chromatography, High Pressure Liquid | Lignans - pharmacology | Lignans - isolation & purification | Gardenia - chemistry | Molecular Structure | HeLa Cells | Circular Dichroism
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13. Full Text Dietary sesamin is converted to enterolactone in humans
by Peñalvo, José L and Heinonen, Satu-M and Aura, Anna-M and Adlercreutz, Herman
Journal of Nutrition, ISSN 0022-3166, 05/2005, Volume 135, Issue 5, pp. 1056 - 1062
Sesamin, a major sesame seed lignan, has many biological actions. The specific mechanisms for most of these actions as well as the full metabolic pathway of... 
Sesame seed | Sesamin | Enterolactone | Enterodiol | Lignans | enterolactone | sesame seed | RATS | enterodiol | lignans | MASS-SPECTROMETRY | BREAST-CANCER | CARDIOVASCULAR HYPERTROPHY | MAMMALIAN LIGNANS | IN-VITRO | NUTRITION & DIETETICS | SERUM CONCENTRATIONS | GAS-CHROMATOGRAPHY | HUMAN FECAL FLORA | sesamin | PLANT LIGNANS | Dioxoles - pharmacokinetics | Humans | Middle Aged | Male | Lignans - metabolism | Intestinal Absorption | 4-Butyrolactone - metabolism | Lignans - administration & dosage | Lignans - pharmacokinetics | Diet | Dioxoles - administration & dosage | Biotransformation | Adult | Female | 4-Butyrolactone - analogs & derivatives | Kinetics | Research | Man | Human beings | Health aspects
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14. Full Text Melanogenesis‐Inhibitory and Antioxidant Activities of Phenolics from Periploca forrestii
by Sun, Cai‐Ling and Chen, Lei and Xu, Jian and Qu, Wei and Guan, Li and Liu, Wen‐Yuan and Akihisa, Toshihiro and Feng, Feng and Zhang, Jie
Chemistry & Biodiversity, ISSN 1612-1872, 08/2017, Volume 14, Issue 8, pp. e1700083 - n/a
Two new tetrahydrofuran‐type lignans, (−)‐gentioluteol 9‐ O ‐ β ‐ d ‐glucopyranoside ( 1 ), (−)‐berchemol 9‐ O ‐ β ‐ d ‐apiofuranosyl‐(1→6)‐ O ‐ β ‐ d... 
Periploca forrestii | Antioxidant abilities | Melanogenesis inhibitory | Tetrahydrofuran‐type lignans | Tetrahydrofuran-type lignans | BARK | BIOCHEMISTRY & MOLECULAR BIOLOGY | LIGNAN | TANNINS | CHEMISTRY, MULTIDISCIPLINARY | PREGNANE GLYCOSIDES | DAMAGE | ACID-DERIVATIVES | STEMS | CHEMICAL-CONSTITUENTS | SKIN | Cell Survival - drug effects | Melanins - antagonists & inhibitors | Microphthalmia-Associated Transcription Factor - metabolism | alpha-MSH - pharmacology | Antioxidants - chemistry | Magnetic Resonance Spectroscopy | Lignans - chemistry | Molecular Conformation | Melanoma, Experimental - pathology | Periploca - chemistry | Melanoma, Experimental - metabolism | Antioxidants - pharmacology | Lignans - pharmacology | Melanins - metabolism | Periploca - metabolism | Animals | Spectrometry, Mass, Electrospray Ionization | Plant Stems - metabolism | Antioxidants - isolation & purification | Cell Line, Tumor | Mice | Plant Stems - chemistry | Circular Dichroism | Lignans - analysis | Antioxidants | Phenols | Medicine, Herbal | Intermedin | Analysis | Medicine, Botanic | Microphthalmia-associated transcription factor | Melanocyte-stimulating hormone | Nuclear magnetic resonance--NMR | Ethanol | Toxicity | Scavenging | Lignans | Stems | Sulfonic acid | Fluorescence recovery after photobleaching | Tetrahydrofuran | Tyrosinase
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15. Full Text Cytotoxic activity of dietary lignan and its derivatives: Structure-cytotoxic activity relationship of dihydroguaiaretic acid
by Wukirsari, Tuti and Nishiwaki, Hisashi and Nishi, Kosuke and Sugahara, Takuya and Akiyama, Koichi and Kishida, Taro and Yamauchi, Satoshi
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 06/2014, Volume 62, Issue 23, pp. 5305 - 5315
Cytotoxic activities of synthesized lignan derivatives were estimated by WST-8 reduction assay against HL-60 and HeLa cells to show the structure-activity... 
dihydroguaiaretic acid | lignan | cytotoxic activity | secoisolariciresinol | ANTIOXIDANT ACTIVITY | FOOD SCIENCE & TECHNOLOGY | AGRICULTURE, MULTIDISCIPLINARY | (-)-MATAIRESINOL | CHEMISTRY, APPLIED | BUTANE-TYPE LIGNANS | Cell Survival - drug effects | Guaiacol - metabolism | Cytotoxins - chemical synthesis | Lignans - chemistry | Humans | Cercopithecus aethiops | Lignans - metabolism | Structure-Activity Relationship | Cytotoxins - toxicity | Animals | Lignans - toxicity | Guaiacol - analogs & derivatives | Cytotoxins - chemistry | Guaiacol - chemical synthesis | Cytotoxins - metabolism | Guaiacol - chemistry | Guaiacol - toxicity | HL-60 Cells | Cell Proliferation - drug effects | Lignans - chemical synthesis | Molecular Structure | Vero Cells | Index Medicus
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16. Full Text Electrophilic Aromatic Deuteration of Lignans: Mostly Reliable but Occasionally Aberrant Selectivities
by Pohjoispää, Monika and Wähälä, Kristiina
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 09/2015, Volume 63, Issue 35, pp. 7595 - 7605
Lignans are a ubiquitous' group of natural products of plant or mammalian origin. In the human diet, especially in fiber-rich foods, there are measurable... 
selectivity | deuteration | stable isotope labeling | lignan | reactivity | STABLE-ISOTOPE-DILUTION | ENTEROLACTONE | MICROWAVE-OVENS | FOOD SCIENCE & TECHNOLOGY | URINARY LIGNANS | INTERNAL STANDARDS | MASS-SPECTROMETRY | DEUTERIUM | BREAST-CANCER | MAMMALIAN LIGNANS | AGRICULTURE, MULTIDISCIPLINARY | CHEMISTRY, APPLIED | PLANT LIGNANS | Animals | Deuterium - metabolism | Lignans - chemistry | Humans | Deuterium - chemistry | Isotope Labeling | Lignans - metabolism | Molecular Structure
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