يعرض 1 - 10 نتائج من 11 نتيجة بحث عن '"Reseda luteola"', وقت الاستعلام: 0.64s تنقيح النتائج
  1. 1
    Glucosinolate profiles and phylogeny in Barbarea compared to other tribe Cardamineae (Brassicaceae) and Reseda (Resedaceae), based on a library of ion trap HPLC-MS/MS data of reference desulfoglucosinolates

    المؤلفون: David I. Pattison, Marcus A. Koch, Marian Ørgaard, Stina Christensen, Conny Bruun Asmussen Lange, Don Cipollini, Karen R. Jensen, Carl Erik Olsen, Christiane Kiefer, Thure P. Hauser, Niels Agerbirk, Cecilie Cetti Hansen

    المصدر: Phytochemistry. 185

    مصطلحات موضوعية: 0106 biological sciences, Barbarea, Barbarea australis, Reseda luteola, Resedaceae, Reseda odorata, Glucosinolates, Plant Science, Horticulture, Nasturtium, 01 natural sciences, Biochemistry, Tandem Mass Spectrometry, Botany, Molecular Biology, Barbarea vulgaris, Chromatography, High Pressure Liquid, Phylogeny, biology, 010405 organic chemistry, General Medicine, biology.organism_classification, 0104 chemical sciences, Europe, Rorippa, Brassicaceae, 010606 plant biology & botany

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47ec92cf60ee41c6505c420caa9d6ae9Test
    https://pubmed.ncbi.nlm.nih.gov/33744557Test


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  2. 2
    Two goitrogenic 1,3-oxazolidine-2-thione derivatives from Brassicales taxa: Challenging identification, occurrence and immunomodulatory effects

    المؤلفون: Milica Todorovska, Dragan B. Zlatković, Pavle J. Randjelović, Niko S. Radulović, Nikola Stojanovic

    المصدر: Food and Chemical Toxicology. 110:94-108

    مصطلحات موضوعية: 0301 basic medicine, Oxazolidine, Chromatography, Gas, Magnetic Resonance Spectroscopy, Reseda luteola, Stereochemistry, Resedaceae, Brassicales, 010402 general chemistry, Toxicology, 01 natural sciences, 03 medical and health sciences, chemistry.chemical_compound, Animals, Humans, Immunologic Factors, Rats, Wistar, Oxazoles, Inflammation, Molecular Structure, biology, Plant Extracts, Thiones, Stereoisomerism, Brassicaceae, General Medicine, biology.organism_classification, Rats, 0104 chemical sciences, 030104 developmental biology, chemistry, Biochemistry, Glucosinolate, Racemic mixture, Enantiomer, Food Science

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33ef80ca8b5a96939c55000895b4cd2fTest
    https://doi.org/10.1016/j.fct.2017.10.005Test


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  3. 3
    Glucosinolate turnover in Brassicales species to an oxazolidin-2-one, formed via the 2-thione and without formation of thioamide

    المؤلفون: Annemarie Matthes, Patrick Rollin, Eleni Lazaridi, Jean-Marc Nuzillard, Pernille Østerbye Erthmann, Caroline Müller, Luisa Ugolini, Susanna Cinti, Søren Bak, Niels Agerbirk, Luca Lazzeri

    المساهمون: Copenhagen Plant Science Center (CPSC), Department of Plant and Environmental Sciences [Copenhagen], Faculty of Science [Copenhagen], University of Copenhagen = Københavns Universitet (UCPH)-University of Copenhagen = Københavns Universitet (UCPH)-Faculty of Science [Copenhagen], University of Copenhagen = Københavns Universitet (UCPH)-University of Copenhagen = Københavns Universitet (UCPH), Consiglio per la Ricerca in Agricoltura e l’analisi dell’economia agraria = Council for Agricultural Research and Economics (CREA), Institut de Chimie Moléculaire de Reims - UMR 7312 (ICMR), Université de Reims Champagne-Ardenne (URCA)-Institut de Chimie du CNRS (INC)-SFR CAP Santé (Champagne-Ardenne Picardie Santé), Université de Reims Champagne-Ardenne (URCA)-Université de Reims Champagne-Ardenne (URCA)-Centre National de la Recherche Scientifique (CNRS)-SFR Condorcet, Université de Reims Champagne-Ardenne (URCA)-Centre National de la Recherche Scientifique (CNRS)-Université de Reims Champagne-Ardenne (URCA)-Centre National de la Recherche Scientifique (CNRS), Universität Bielefeld = Bielefeld University, Institut de Chimie Organique et Analytique (ICOA), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université d'Orléans (UO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), University of Copenhagen = Københavns Universitet (KU)-University of Copenhagen = Københavns Universitet (KU)-Faculty of Science [Copenhagen], University of Copenhagen = Københavns Universitet (KU)-University of Copenhagen = Københavns Universitet (KU), Consiglio per la Ricerca in Agricoltura e l’analisi dell’economia agraria (CREA), SFR Condorcet, Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-SFR CAP Santé (Champagne-Ardenne Picardie Santé), Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Université d'Orléans (UO)-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut de Chimie du CNRS (INC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Nuzillard, Jean-Marc, Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-SFR Condorcet, Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Phytochemistry
    Phytochemistry, 2018, 153, pp.79-93. ⟨10.1016/j.phytochem.2018.05.006⟩
    Phytochemistry, Elsevier, 2018, 153, pp.79-93. ⟨10.1016/j.phytochem.2018.05.006⟩

    مصطلحات موضوعية: 0106 biological sciences, 0301 basic medicine, Reseda luteola, Glucosinolate hydrolysis, Resedaceae, Glucosinolates, Brassicales, Plant Science, Horticulture, 01 natural sciences, Biochemistry, [SDV.BV.BOT] Life Sciences [q-bio]/Vegetal Biology/Botanics, 03 medical and health sciences, chemistry.chemical_compound, Species Specificity, Barbarea vulgaris R.Br. (Brassicaceae), [SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biochemistry [q-bio.BM], [SDV.BBM.BC] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biochemistry [q-bio.BM], Molecular Biology, Oxazolidinones, Barbarea vulgaris, Thioamide, chemistry.chemical_classification, Molecular Structure, biology, 1 3-Oxazolidin-2-one, Thiones, Brassicaceae, General Medicine, [SDV.BV.BOT]Life Sciences [q-bio]/Vegetal Biology/Botanics, biology.organism_classification, Turnover, Barbarea vulgaris R.Br. (Brassicaceae) Glucosinolate hydrolysis Turnover 1,3-Oxazolidine-2-thione 1,3-Oxazolidin-2-one Nitrile Thioamide Reseda luteola Nasturtium officinale, Thioamides, 030104 developmental biology, Enzyme, chemistry, Glucosinolate, 1 3-Oxazolidine-2-thione, Silique, Nitrile, Nasturtium officinale, 010606 plant biology & botany

    وصف الملف: application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30426ef014db9065cf10f1e14ffaf773Test
    https://hal.univ-reims.fr/hal-01904913/documentTest


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  4. 4
    Fast chromatographic separation for the quantitation of the main flavone dyes in Reseda luteola (weld)

    المؤلفون: Goverdina C. H. Derksen, Teris A. van Beek, Eric Simon Gabriel Maria Mattheussens, Alexandre Villela, Han Zuilhof, Elbert J.C. van der Klift

    المصدر: Journal of Chromatography. A, Including electrophoresis and other separation methods, 1218(47), 8544-8550
    Journal of Chromatography. A, Including electrophoresis and other separation methods 1218 (2011) 47

    مصطلحات موضوعية: Reseda luteola, Sensitivity and Specificity, Biochemistry, Flavones, High-performance liquid chromatography, Statistics, Nonparametric, l, Analytical Chemistry, chemistry.chemical_compound, bilobalide, Glucosides, Maceration (wine), Resedaceae, diode-array detection, Coloring Agents, Chromatography, High Pressure Liquid, VLAG, chemistry.chemical_classification, Detection limit, performance liquid-chromatography, Chromatography, biology, Plant Extracts, Chemistry, Methanol, Extraction (chemistry), Organic Chemistry, Reproducibility of Results, General Medicine, biology.organism_classification, portugal, Organische Chemie, quantification, Textile Industry, Linear Models, identification, Luteolin, Natural dye

    وصف الملف: application/octet-stream; application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc543cc17e0924de8660fda0dc421de1Test
    https://doi.org/10.1016/j.chroma.2011.09.069Test


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  5. 5
    Characterization of weld (Reseda luteola L.) and spurge flax (Daphne gnidium L.) by high-performance liquid chromatography–diode array detection–mass spectrometry in Arraiolos historical textiles

    المؤلفون: Maria João Melo, Micaela M. Sousa, Rita Marques, Maria Cristina Oliveira

    المصدر: Journal of Chromatography A. 1216:1395-1402

    مصطلحات موضوعية: Reseda luteola, Biochemistry, High-performance liquid chromatography, Mass Spectrometry, Indigo, Analytical Chemistry, History, 17th Century, Liquid chromatography–mass spectrometry, Floors and Floorcoverings, Resedaceae, Glycosides, Coloring Agents, Chromatography, High Pressure Liquid, Flavonoids, Chromatography, biology, Plant Extracts, Chemistry, Textiles, Organic Chemistry, Extraction (chemistry), General Medicine, biology.organism_classification, Daphne gnidium, Daphne, Dyeing, Natural dye, Chromatography, Liquid

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc40f012abc48a20e540ec3161995bcfTest
    https://doi.org/10.1016/j.chroma.2008.12.083Test


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  6. 6
    In vitro antibacterial and antitumor activities of some medicinal plant extracts, growing in Turkey

    المؤلفون: Fatma Pehlivan Karakas, Arzu Ucar Turker, Arzu Birinci Yildirim

    المساهمون: BAİBÜ, Fen Edebiyat Fakültesi, Biyoloji Bölümü, Yıldırım, Arzu Birinci, Karakaş, Fatma Pehlivan, Türker, Arzu Uçar

    المصدر: Asian Pacific journal of tropical medicine. 6(8)

    مصطلحات موضوعية: Reseda luteola, Turkey, Antineoplastic Agents, Biology, Ajuga, Bioassays, food, Plant Tumors, Stellaria media, Botany, Medicinal Plants, Humans, Nymphaea alba, Medicine(all), Plants, Medicinal, Traditional medicine, Bacteria, Plant Extracts, General Medicine, Antitumor, biology.organism_classification, Vinca minor, food.food, Anti-Bacterial Agents, Antibacterial, Phlomis, Antibacterial activity, Marrubium

    وصف الملف: application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7b8c12706dbe05eebde1ccc56f795f6Test
    https://pubmed.ncbi.nlm.nih.gov/23790332Test


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  7. 7
    Acidic amino acids in Reseda luteola

    المؤلفون: Hilmer Sørensen, Ole Olsen, Lene Kaa Meier

    المصدر: Phytochemistry. 18:1505-1509

    مصطلحات موضوعية: Alanine, chemistry.chemical_classification, Reseda luteola, biology, Chemistry, Stereochemistry, Diastereomer, Plant Science, General Medicine, Glutathione, Horticulture, biology.organism_classification, Biochemistry, Amino acid, chemistry.chemical_compound, Acidic amino acids, Glycine, Organic chemistry, Molecular Biology

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b89ef1aac3661e57c3297ea1601e4ab0Test
    https://doi.org/10.1016/s0031-9422Test(00)98484-x


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  8. 8
    Dosage densitométrique direct par réflexion des flavonoïdes de la gaude Reseda luteola L.) séparés par chromatographie sur couche mince

    المؤلفون: A. Jacquin-Dubreuil

    المصدر: Journal of Chromatography A. 72:487-498

    مصطلحات موضوعية: Reseda luteola, Chromatography, medicine.diagnostic_test, biology, Organic Chemistry, Thin layer, General Medicine, biology.organism_classification, Biochemistry, Analytical Chemistry, Standard curve, chemistry.chemical_compound, chemistry, Spectrophotometry, medicine, Luteolin

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0c8a905b4162a12ddcf752dae13621b8Test
    https://doi.org/10.1016/s0021-9673Test(01)91903-x


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  9. 9
    l-2-amino-4-phenylbutyric acid and 2-phenylethylglucosinolate, precursors of 2-hydroxy-2-phenylethylglucosinolate

    المؤلفون: D.F. Kirkland, E. W. Underhill

    المصدر: Phytochemistry. 11:1973-1979

    مصطلحات موضوعية: Reseda luteola, biology, Stereochemistry, chemistry.chemical_element, Phenylalanine, Plant Science, General Medicine, Horticulture, biology.organism_classification, Biochemistry, Nitrogen, PHENYLBUTYRIC ACID, chemistry.chemical_compound, Aglycone, chemistry, Biosynthesis, Glucosinolate, Organic chemistry, Molecular Biology

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::87b794637d074d93f96b01f5c72ffb2fTest
    https://doi.org/10.1016/s0031-9422Test(00)90161-4


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  10. 10
    ChemInform Abstract: Total Synthesis of (.+-.)-Resedine and (.+-.)-Resedinine Alkaloids from Reseda luteola

    المؤلفون: J. B. Mieczkowski

    المصدر: ChemInform. 18

    مصطلحات موضوعية: Reseda luteola, biology, Chemistry, Botany, Total synthesis, General Medicine, biology.organism_classification

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::f367facb21f62d6bfe098e7aa1fc73a2Test
    https://doi.org/10.1002/chin.198702328Test


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