Food Chemistry, ISSN 0308-8146, 06/2017, Volume 224, pp. 390 - 397
In this research, honey samples were adulterated with date syrup (DS) and invert sugar syrup (IS) at three concentrations (7%, 15% and 30%). 102 adulterated...
Multivariate analysis | Honey adulteration | Physicochemical properties | FOOD SCIENCE & TECHNOLOGY | BLOSSOM | SUGAR SYRUPS | PHYSICOCHEMICAL PARAMETERS | FLORAL ORIGIN | NUTRITION & DIETETICS | CHEMICAL MEASURANDS | DISCRIMINATION | DSC | SAMPLES | CHEMISTRY, APPLIED | FOOD | Multivariate Analysis | Food Contamination - analysis | Rheology | Fructose - analysis | Chemical Phenomena | Honey - analysis | Sucrose - analysis | Glucose - analysis | Phoeniceae - chemistry | Principal Component Analysis | Discriminant Analysis | Index Medicus
Multivariate analysis | Honey adulteration | Physicochemical properties | FOOD SCIENCE & TECHNOLOGY | BLOSSOM | SUGAR SYRUPS | PHYSICOCHEMICAL PARAMETERS | FLORAL ORIGIN | NUTRITION & DIETETICS | CHEMICAL MEASURANDS | DISCRIMINATION | DSC | SAMPLES | CHEMISTRY, APPLIED | FOOD | Multivariate Analysis | Food Contamination - analysis | Rheology | Fructose - analysis | Chemical Phenomena | Honey - analysis | Sucrose - analysis | Glucose - analysis | Phoeniceae - chemistry | Principal Component Analysis | Discriminant Analysis | Index Medicus
Journal Article
Journal of the American Heart Association, ISSN 2047-9980, 07/2016, Volume 5, Issue 7, p. n/a
Background Our dual aims were as follows: (1) to classify new or recurrent myocardial infarctions (MI) in patients with stable atherosclerosis using the...
atherosclerosis | cardiovascular disease | myocardial infarction | platelet inhibitor | DEFINITION | CARDIAC & CARDIOVASCULAR SYSTEMS | TRITON-TIMI 38 | CARDIOVASCULAR DEATH | VORAPAXAR | PRASUGREL | Recurrence | Myocardial Infarction - epidemiology | Atherosclerosis - drug therapy | Myocardial Infarction - classification | Humans | Middle Aged | Peripheral Arterial Disease - drug therapy | Proportional Hazards Models | Male | Secondary Prevention | Coronary Artery Disease - drug therapy | Lactones - therapeutic use | Randomized Controlled Trials as Topic | Female | Aged | Myocardial Infarction - prevention & control | Platelet Aggregation Inhibitors - therapeutic use | Pyridines - therapeutic use
atherosclerosis | cardiovascular disease | myocardial infarction | platelet inhibitor | DEFINITION | CARDIAC & CARDIOVASCULAR SYSTEMS | TRITON-TIMI 38 | CARDIOVASCULAR DEATH | VORAPAXAR | PRASUGREL | Recurrence | Myocardial Infarction - epidemiology | Atherosclerosis - drug therapy | Myocardial Infarction - classification | Humans | Middle Aged | Peripheral Arterial Disease - drug therapy | Proportional Hazards Models | Male | Secondary Prevention | Coronary Artery Disease - drug therapy | Lactones - therapeutic use | Randomized Controlled Trials as Topic | Female | Aged | Myocardial Infarction - prevention & control | Platelet Aggregation Inhibitors - therapeutic use | Pyridines - therapeutic use
Journal Article
Journal of Pharmaceutical and Biomedical Analysis, ISSN 0731-7085, 09/2018, Volume 158, pp. 151 - 159
The growing interest in assuring phytomedicines efficacy and moreover the increase in requirements for its safety drive the development of analytical methods...
Phytomedicines | Fingerprinting | Phytoequivalency | Artichoke | PCA | CHEMISTRY, ANALYTICAL | UPLC-MS | NMR TECHNIQUES | PHENOLIC COMPOSITION | HERBAL PRODUCTS | IDENTIFICATION | CYNARA-SCOLYMUS L | CHEMOMETRICS | PHARMACOLOGY & PHARMACY | EXTRACTS | TRIGONELLINE | MULTIPLEX APPROACH | Flavones | Bioflavonoids | Liver | Drugstores | Fatty acids | Lactones | Flavonoids | Metabolites | Sesquiterpenes | Medicine, Botanic | Pharmacy | Polyphenols | Medicine, Herbal
Phytomedicines | Fingerprinting | Phytoequivalency | Artichoke | PCA | CHEMISTRY, ANALYTICAL | UPLC-MS | NMR TECHNIQUES | PHENOLIC COMPOSITION | HERBAL PRODUCTS | IDENTIFICATION | CYNARA-SCOLYMUS L | CHEMOMETRICS | PHARMACOLOGY & PHARMACY | EXTRACTS | TRIGONELLINE | MULTIPLEX APPROACH | Flavones | Bioflavonoids | Liver | Drugstores | Fatty acids | Lactones | Flavonoids | Metabolites | Sesquiterpenes | Medicine, Botanic | Pharmacy | Polyphenols | Medicine, Herbal
Journal Article
Journal of Separation Science, ISSN 1615-9306, 04/2016, Volume 39, Issue 7, pp. 1286 - 1294
Analytical methods using high‐performance liquid chromatography with diode array and tandem mass spectrometry detection were developed for the discrimination...
Atractylodes plants | Liquid chromatography | Multivariate statistical analysis | Quality control | Quantitative analysis | CHEMISTRY, ANALYTICAL | ANTIINFLAMMATORY ACTIVITY | ATRACTYLENOLIDE-III | ESSENTIAL OIL | SOLID-PHASE MICROEXTRACTION | VOLATILE COMPOUNDS | IDENTIFICATION | LANCEA | GC-MS | EXTRACTION | MACROCEPHALA | Plants, Medicinal - classification | Multivariate Analysis | Tandem Mass Spectrometry | Plants, Medicinal - chemistry | Rhizome - chemistry | Sesquiterpenes - analysis | Chromatography, High Pressure Liquid | Lactones - analysis | Atractylodes - chemistry | Furans - analysis | Circuit components | Medicinal plants | Analysis | Medicine, Botanic | Medicine, Herbal | Mass spectrometry | High performance liquid chromatography | Herbal medicine | Scientific imaging | Statistical analysis | Chromatography | Samples | Plants (organisms) | Statistical methods | Arrays | Diodes
Atractylodes plants | Liquid chromatography | Multivariate statistical analysis | Quality control | Quantitative analysis | CHEMISTRY, ANALYTICAL | ANTIINFLAMMATORY ACTIVITY | ATRACTYLENOLIDE-III | ESSENTIAL OIL | SOLID-PHASE MICROEXTRACTION | VOLATILE COMPOUNDS | IDENTIFICATION | LANCEA | GC-MS | EXTRACTION | MACROCEPHALA | Plants, Medicinal - classification | Multivariate Analysis | Tandem Mass Spectrometry | Plants, Medicinal - chemistry | Rhizome - chemistry | Sesquiterpenes - analysis | Chromatography, High Pressure Liquid | Lactones - analysis | Atractylodes - chemistry | Furans - analysis | Circuit components | Medicinal plants | Analysis | Medicine, Botanic | Medicine, Herbal | Mass spectrometry | High performance liquid chromatography | Herbal medicine | Scientific imaging | Statistical analysis | Chromatography | Samples | Plants (organisms) | Statistical methods | Arrays | Diodes
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2018, Volume 13, Issue 5, p. e0198010
For about 70 years, L-glucose had been considered non-metabolizable by either mammalian or bacterial cells. Recently, however, an L-glucose catabolic pathway...
FRUCTOSE OXIDOREDUCTASE | SYSTEM | ZYMOMONAS-MOBILIS | MYOINOSITOL DEHYDROGENASE | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | Physiological aspects | Glucose metabolism | Oxidoreductases | Research | Properties | Structure | Residues | Dehydrogenases | Genomics | Genes | Biochemistry | Catalytic activity | Phylogeny | Glucose | Dehydrogenase | Proteins | Glucose dehydrogenase | E coli | Polyethylene glycol | Oxidation | Catalysis | Sugar | Crystal structure | Enzymes | Inositol | Cloning | Substrates | NAD | Inositols | Environmental science | Mutagenesis | Site-directed mutagenesis | Recognition
FRUCTOSE OXIDOREDUCTASE | SYSTEM | ZYMOMONAS-MOBILIS | MYOINOSITOL DEHYDROGENASE | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | Physiological aspects | Glucose metabolism | Oxidoreductases | Research | Properties | Structure | Residues | Dehydrogenases | Genomics | Genes | Biochemistry | Catalytic activity | Phylogeny | Glucose | Dehydrogenase | Proteins | Glucose dehydrogenase | E coli | Polyethylene glycol | Oxidation | Catalysis | Sugar | Crystal structure | Enzymes | Inositol | Cloning | Substrates | NAD | Inositols | Environmental science | Mutagenesis | Site-directed mutagenesis | Recognition
Journal Article
Molecular Phylogenetics and Evolution, ISSN 1055-7903, 2009, Volume 52, Issue 1, pp. 142 - 156
With an estimated 300–375 species, is the largest genus of Porellales and forms a major clade of leafy liverworts. The cosmopolitan genus includes mostly...
Jungermanniopsida | Molecular phylogeny | Frullaniaceae | Amphijubula | Schusterella | Frullania | Porellales | Neohattoria | MORPHOLOGICAL INCONGRUENCE | NRITS SEQUENCES | ANNOTATED CHECKLIST | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHLOROPLAST DNA-SEQUENCES | SESQUITERPENE LACTONES | EVOLUTIONARY BIOLOGY | LEJEUNEACEAE JUNGERMANNIOPSIDA | NATURAL CLASSIFICATION | CRYPTIC SPECIATION | GENETICS & HEREDITY | GENUS FRULLANIA | LIVERWORTS MARCHANTIOPHYTA | Sequence Alignment | Cell Nucleus - genetics | Genes, Plant | Genetic Speciation | Hepatophyta - classification | DNA, Chloroplast - genetics | Hepatophyta - genetics | Models, Genetic | Phylogeny | Sequence Analysis, DNA | DNA, Plant - genetics | Evolution, Molecular | Museums | Natural history
Jungermanniopsida | Molecular phylogeny | Frullaniaceae | Amphijubula | Schusterella | Frullania | Porellales | Neohattoria | MORPHOLOGICAL INCONGRUENCE | NRITS SEQUENCES | ANNOTATED CHECKLIST | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHLOROPLAST DNA-SEQUENCES | SESQUITERPENE LACTONES | EVOLUTIONARY BIOLOGY | LEJEUNEACEAE JUNGERMANNIOPSIDA | NATURAL CLASSIFICATION | CRYPTIC SPECIATION | GENETICS & HEREDITY | GENUS FRULLANIA | LIVERWORTS MARCHANTIOPHYTA | Sequence Alignment | Cell Nucleus - genetics | Genes, Plant | Genetic Speciation | Hepatophyta - classification | DNA, Chloroplast - genetics | Hepatophyta - genetics | Models, Genetic | Phylogeny | Sequence Analysis, DNA | DNA, Plant - genetics | Evolution, Molecular | Museums | Natural history
Journal Article
7.
Full Text
Structure-function analysis identifies highly sensitive strigolactone receptors in Striga
Science, ISSN 0036-8075, 10/2015, Volume 350, Issue 6257, pp. 203 - 207
Strigolactones are naturally occurring signaling molecules that affect plant development, fungi-plant interactions, and parasitic plant infestations. We...
PERCEPTION | MULTIDISCIPLINARY SCIENCES | HERMONTHICA | ARABIDOPSIS | GERMINATION | PARASITIC PLANTS | RICE | Heterocyclic Compounds, 3-Ring - metabolism | Heterocyclic Compounds, 3-Ring - pharmacology | Molecular Sequence Data | Structure-Activity Relationship | Phylogeny | Striga - genetics | Lactones - pharmacology | Plant Proteins - classification | Seeds - growth & development | Plant Proteins - chemistry | Striga - growth & development | Receptors, Cell Surface - chemistry | Germination - drug effects | Amino Acid Sequence | Catalytic Domain | Seeds - metabolism | Protein Structure, Secondary | Seeds - genetics | Lactones - metabolism | Striga - metabolism | Arabidopsis - metabolism | Receptors, Cell Surface - classification | Arabidopsis - genetics | Plant Proteins - genetics | Plant Growth Regulators - metabolism | Plant Growth Regulators - pharmacology | Receptors, Cell Surface - genetics | Arabidopsis thaliana | Analysis | Physiological aspects | Lamiales | Hormone receptors | Plant hormones | Identification and classification | Fungi | Molecules | Flowers & plants | Hormones | Parasites | Weeds | Binding | Receptors | Pocket | Plants (organisms) | Biology | Crystal structure
PERCEPTION | MULTIDISCIPLINARY SCIENCES | HERMONTHICA | ARABIDOPSIS | GERMINATION | PARASITIC PLANTS | RICE | Heterocyclic Compounds, 3-Ring - metabolism | Heterocyclic Compounds, 3-Ring - pharmacology | Molecular Sequence Data | Structure-Activity Relationship | Phylogeny | Striga - genetics | Lactones - pharmacology | Plant Proteins - classification | Seeds - growth & development | Plant Proteins - chemistry | Striga - growth & development | Receptors, Cell Surface - chemistry | Germination - drug effects | Amino Acid Sequence | Catalytic Domain | Seeds - metabolism | Protein Structure, Secondary | Seeds - genetics | Lactones - metabolism | Striga - metabolism | Arabidopsis - metabolism | Receptors, Cell Surface - classification | Arabidopsis - genetics | Plant Proteins - genetics | Plant Growth Regulators - metabolism | Plant Growth Regulators - pharmacology | Receptors, Cell Surface - genetics | Arabidopsis thaliana | Analysis | Physiological aspects | Lamiales | Hormone receptors | Plant hormones | Identification and classification | Fungi | Molecules | Flowers & plants | Hormones | Parasites | Weeds | Binding | Receptors | Pocket | Plants (organisms) | Biology | Crystal structure
Journal Article
Molecules (Basel, Switzerland), ISSN 1420-3049, 07/2018, Volume 23, Issue 8, p. 1907
Piper methysticum (kava) root is known to possess promising weed suppressing activity. The present study was conducted to search for potent plant growth...
Piper methysticum L | flavanone | growth inhibitor | natural herbicide | Raphanus sativus | kavalactone | ALLELOCHEMICALS | ANTIOXIDANT ACTIVITIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | LEAVES | PERS. BL BURTT | KAVA HEPATOTOXICITY | ALPINIA-ZERUMBET | IDENTIFICATION | PYRONES | CHEMISTRY, MULTIDISCIPLINARY | LACTONES | RM SM | Flavanones - isolation & purification | Plant Extracts - chemistry | Plant Weeds - growth & development | Gas Chromatography-Mass Spectrometry | Solvents - chemistry | Acetates - chemistry | Plant Growth Regulators - classification | Lactones - pharmacology | Lactones - classification | Molecular Structure | Weed Control - methods | Kava - metabolism | Plant Growth Regulators - isolation & purification | Plant Weeds - drug effects | Plant Roots - metabolism | Lactones - isolation & purification | Flavanones - pharmacology | Herbicides - classification | Kava - chemistry | Herbicides - pharmacology | Flavanones - classification | Herbicides - isolation & purification | Raphanus - growth & development | Raphanus - drug effects | Plant Roots - chemistry | Plant Growth Regulators - pharmacology | Plants, Medicinal | Medicinal plants | Spectroscopy | Nuclear magnetic resonance--NMR | Purification | Ethyl acetate | Mass spectroscopy | Chromatography | Weight | Plant extracts | Gas chromatography | Inhibitors | Plant growth | Ionization | Scientific imaging | Acetic acid | Mass spectrometry | Column chromatography | Elongation
Piper methysticum L | flavanone | growth inhibitor | natural herbicide | Raphanus sativus | kavalactone | ALLELOCHEMICALS | ANTIOXIDANT ACTIVITIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | LEAVES | PERS. BL BURTT | KAVA HEPATOTOXICITY | ALPINIA-ZERUMBET | IDENTIFICATION | PYRONES | CHEMISTRY, MULTIDISCIPLINARY | LACTONES | RM SM | Flavanones - isolation & purification | Plant Extracts - chemistry | Plant Weeds - growth & development | Gas Chromatography-Mass Spectrometry | Solvents - chemistry | Acetates - chemistry | Plant Growth Regulators - classification | Lactones - pharmacology | Lactones - classification | Molecular Structure | Weed Control - methods | Kava - metabolism | Plant Growth Regulators - isolation & purification | Plant Weeds - drug effects | Plant Roots - metabolism | Lactones - isolation & purification | Flavanones - pharmacology | Herbicides - classification | Kava - chemistry | Herbicides - pharmacology | Flavanones - classification | Herbicides - isolation & purification | Raphanus - growth & development | Raphanus - drug effects | Plant Roots - chemistry | Plant Growth Regulators - pharmacology | Plants, Medicinal | Medicinal plants | Spectroscopy | Nuclear magnetic resonance--NMR | Purification | Ethyl acetate | Mass spectroscopy | Chromatography | Weight | Plant extracts | Gas chromatography | Inhibitors | Plant growth | Ionization | Scientific imaging | Acetic acid | Mass spectrometry | Column chromatography | Elongation
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 10/2016, Volume 479, Issue 4, pp. 622 - 627
The Andes-endemic Barnadesioideae lineage is the oldest surviving and phylogenetically basal subfamily of the Asteraceae (Compositae), a prolific group of...
Terpene synthase | Sesquiterpene lactone | Barnadesia spinosa | Germacrene A synthase | Asteraceae | ANTIMALARIAL-DRUG PRECURSOR | EVOLUTIONARY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CLASSIFICATION | NEURAL-NETWORKS | BIOPHYSICS | CLONING | GENES | EXPRESSION | Alkyl and Aryl Transferases - classification | Alkyl and Aryl Transferases - chemistry | Asteraceae - enzymology | Alkyl and Aryl Transferases - metabolism | Sesquiterpenes, Germacrane - biosynthesis | Phylogeny | Biodiversity | Lactones - metabolism | Asteraceae - classification | Plant Proteins - genetics | Plant Proteins - classification | Alkyl and Aryl Transferases - genetics | Plant Proteins - chemistry | Asteraceae - genetics | Cloning, Molecular | Sesquiterpenes, Germacrane - chemistry | Plant Proteins - metabolism | Kinetics | Oxidases | Physiological aspects | Cladistic analysis | Metabolites | Analysis | Enzymes | LACTONES | SOUTH AMERICA | 60 APPLIED LIFE SCIENCES | BIOSYNTHESIS
Terpene synthase | Sesquiterpene lactone | Barnadesia spinosa | Germacrene A synthase | Asteraceae | ANTIMALARIAL-DRUG PRECURSOR | EVOLUTIONARY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CLASSIFICATION | NEURAL-NETWORKS | BIOPHYSICS | CLONING | GENES | EXPRESSION | Alkyl and Aryl Transferases - classification | Alkyl and Aryl Transferases - chemistry | Asteraceae - enzymology | Alkyl and Aryl Transferases - metabolism | Sesquiterpenes, Germacrane - biosynthesis | Phylogeny | Biodiversity | Lactones - metabolism | Asteraceae - classification | Plant Proteins - genetics | Plant Proteins - classification | Alkyl and Aryl Transferases - genetics | Plant Proteins - chemistry | Asteraceae - genetics | Cloning, Molecular | Sesquiterpenes, Germacrane - chemistry | Plant Proteins - metabolism | Kinetics | Oxidases | Physiological aspects | Cladistic analysis | Metabolites | Analysis | Enzymes | LACTONES | SOUTH AMERICA | 60 APPLIED LIFE SCIENCES | BIOSYNTHESIS
Journal Article
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Book
Reproductive Toxicology, ISSN 0890-6238, 2009, Volume 28, Issue 3, pp. 285 - 296
Single oral doses of artesunate, dihydroartemisinin, arteether and artemether administered to rats during a sensitive period of organogenesis caused embryo...
Dihydroartemisinin | Embryotoxicity | Artesunate | Artemisinin antimalarial | Artemether | Reticulocytes | Teratogen | Arteether | UNCOMPLICATED FALCIPARUM-MALARIA | COMBINATION THERAPY | DEVELOPMENTAL TOXICITY | REPRODUCTIVE BIOLOGY | INTRAVENOUS ARTESUNATE | ORAL ARTESUNATE | PLASMODIUM-FALCIPARUM | TISSUE DISTRIBUTION | EMBRYONIC ERYTHROBLASTS | TOXICOLOGY | HEALTHY-VOLUNTEERS | BLOOD-CELLS | Embryo, Mammalian - drug effects | Teratogens - toxicity | Heart Septal Defects, Ventricular - chemically induced | Species Specificity | Artemisinins - toxicity | Humans | Macaca fascicularis | Pregnancy Trimester, First | Bone and Bones - drug effects | Lactones - classification | Maternal Exposure - adverse effects | Adult | Female | Teratogens - classification | Erythroblasts - drug effects | Rabbits | Heart Septal Defects, Ventricular - embryology | Embryo Loss - chemically induced | Risk Assessment | Rats | Lactones - toxicity | Pregnancy | Animals | Abnormalities, Drug-Induced - etiology | Artemisinins - classification | Antimalarials - classification | Antimalarials - toxicity | Bone and Bones - abnormalities | Erythroblasts - pathology | Monkeys | Pregnant women | Developmental biology | Index Medicus
Dihydroartemisinin | Embryotoxicity | Artesunate | Artemisinin antimalarial | Artemether | Reticulocytes | Teratogen | Arteether | UNCOMPLICATED FALCIPARUM-MALARIA | COMBINATION THERAPY | DEVELOPMENTAL TOXICITY | REPRODUCTIVE BIOLOGY | INTRAVENOUS ARTESUNATE | ORAL ARTESUNATE | PLASMODIUM-FALCIPARUM | TISSUE DISTRIBUTION | EMBRYONIC ERYTHROBLASTS | TOXICOLOGY | HEALTHY-VOLUNTEERS | BLOOD-CELLS | Embryo, Mammalian - drug effects | Teratogens - toxicity | Heart Septal Defects, Ventricular - chemically induced | Species Specificity | Artemisinins - toxicity | Humans | Macaca fascicularis | Pregnancy Trimester, First | Bone and Bones - drug effects | Lactones - classification | Maternal Exposure - adverse effects | Adult | Female | Teratogens - classification | Erythroblasts - drug effects | Rabbits | Heart Septal Defects, Ventricular - embryology | Embryo Loss - chemically induced | Risk Assessment | Rats | Lactones - toxicity | Pregnancy | Animals | Abnormalities, Drug-Induced - etiology | Artemisinins - classification | Antimalarials - classification | Antimalarials - toxicity | Bone and Bones - abnormalities | Erythroblasts - pathology | Monkeys | Pregnant women | Developmental biology | Index Medicus
Journal Article
Phytochemistry, ISSN 0031-9422, 2005, Volume 66, Issue 3, pp. 345 - 353
Encoded 3D structures of sesquiterpene lactones of three tribes of the family Asteraceae were projected into self-organizing maps allowing the prediction of...
Taxonomic markers | Sesquiterpene lactones | 3D structures | Asteraceae | Kohonen networks | Chemosystematics | Chemotaxonomy | Chemoinformatics | Asteraceae - chemistry | Sesquiterpenes - chemistry | Sesquiterpenes - analysis | Classification - methods | Molecular Structure | Lactones - analysis | Asteraceae - classification | Lactones - chemistry | Neural Networks (Computer)
Taxonomic markers | Sesquiterpene lactones | 3D structures | Asteraceae | Kohonen networks | Chemosystematics | Chemotaxonomy | Chemoinformatics | Asteraceae - chemistry | Sesquiterpenes - chemistry | Sesquiterpenes - analysis | Classification - methods | Molecular Structure | Lactones - analysis | Asteraceae - classification | Lactones - chemistry | Neural Networks (Computer)
Journal Article
Journal of Chemical Information and Modeling, ISSN 1549-9596, 01/2008, Volume 48, Issue 1, pp. 56 - 67
Recently, we have built a classification model that is capable of assigning a given sesquiterpene lactone (STL) into exactly one tribe of the plant family...
Terpenes - chemistry | Plants - metabolism | Sesquiterpenes - chemistry | Terpenes - isolation & purification | Terpenes - metabolism | Artificial Intelligence | Computer Simulation | Plants - chemistry | Plants - classification | Lactones - chemistry
Terpenes - chemistry | Plants - metabolism | Sesquiterpenes - chemistry | Terpenes - isolation & purification | Terpenes - metabolism | Artificial Intelligence | Computer Simulation | Plants - chemistry | Plants - classification | Lactones - chemistry
Journal Article
Chemical Reviews, ISSN 0009-2665, 06/2014, Volume 114, Issue 12, pp. 6213 - 6284
CHIRAL 3-SUBSTITUTED PHTHALIDES | HALOGEN-LITHIUM EXCHANGE | ONE-POT SYNTHESIS | PALLADIUM-CATALYZED SYNTHESIS | DIRECTED ORTHO-METALATION | DIELS-ALDER REACTION | 1ST TOTAL-SYNTHESIS | ARYL ADDITION/INTRAMOLECULAR LACTONIZATION | SECONDARY MOLD METABOLITES | CNIDIUM-OFFICINALE MAKINO | CHEMISTRY, MULTIDISCIPLINARY | Oxidation-Reduction | Benzoates - chemistry | Bacteria - drug effects | Phthalimides - classification | Benzofurans - chemical synthesis | Benzofurans - pharmacology | Biological Products - pharmacology | Benzofurans - classification | Anti-Bacterial Agents - chemical synthesis | Biological Products - chemical synthesis | Phthalimides - pharmacology | Biological Products - chemistry | Phthalimides - chemical synthesis | Cyclization | Anti-Bacterial Agents - chemistry | Anti-Bacterial Agents - pharmacology | Lactones - chemistry | Chemical properties | Research | Chemical synthesis | Phthalates | Methods
Journal Article
Journal of Chemical Information and Modeling, ISSN 1549-9596, 01/2007, Volume 47, Issue 1, pp. 9 - 19
In a recent publication we described the application of an unsupervised learning method using self-organizing maps to the separation of three tribes and seven...
SECONDARY METABOLITES | COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS | EVOLUTION | NOVELTY DETECTION | NATURAL SESQUITERPENOIDS | COMPUTER SCIENCE, INFORMATION SYSTEMS | SPECTRA | CHEMISTRY, MULTIDISCIPLINARY | Asteraceae - chemistry | Expert Systems | Models, Biological | Sesquiterpenes | Classification | Probability | Models, Statistical | Plants - chemistry | Plants - classification | Asteraceae - classification | Lactones | Neural Networks (Computer)
SECONDARY METABOLITES | COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS | EVOLUTION | NOVELTY DETECTION | NATURAL SESQUITERPENOIDS | COMPUTER SCIENCE, INFORMATION SYSTEMS | SPECTRA | CHEMISTRY, MULTIDISCIPLINARY | Asteraceae - chemistry | Expert Systems | Models, Biological | Sesquiterpenes | Classification | Probability | Models, Statistical | Plants - chemistry | Plants - classification | Asteraceae - classification | Lactones | Neural Networks (Computer)
Journal Article
Journal of the Serbian Chemical Society, ISSN 0352-5139, 2010, Volume 75, Issue 7, pp. 875 - 891
The chemical composition of polyphenols in tobacco waste was identified by HPLC-PDA-ESI/MS/MS and the contents of chlorogenic acids and rutin in 10 varieties...
Multivariate statistical analysis | HPLC-PDA-ESI/MS/MS | Rutin | Tobacco (Nicotiana tabacum L.) waste | Chlorogenic acids | PHENOLIC-COMPOUNDS | MSN | FLAVONOIDS | rutin | chlorogenic acids | CHEMISTRY, MULTIDISCIPLINARY | FLIGHT MASS-SPECTROMETRY | LIQUID-CHROMATOGRAPHY | GAS-CHROMATOGRAPHY | FINGERPRINT | LACTONES | DERIVATIVES | tobacco (Nicotiana tabacum L.) waste | multivariate statistical analysis | HPLC–PDA–ESI/MS/MS
Multivariate statistical analysis | HPLC-PDA-ESI/MS/MS | Rutin | Tobacco (Nicotiana tabacum L.) waste | Chlorogenic acids | PHENOLIC-COMPOUNDS | MSN | FLAVONOIDS | rutin | chlorogenic acids | CHEMISTRY, MULTIDISCIPLINARY | FLIGHT MASS-SPECTROMETRY | LIQUID-CHROMATOGRAPHY | GAS-CHROMATOGRAPHY | FINGERPRINT | LACTONES | DERIVATIVES | tobacco (Nicotiana tabacum L.) waste | multivariate statistical analysis | HPLC–PDA–ESI/MS/MS
Journal Article