Biochemistry, ISSN 0006-2960, 03/2017, Volume 56, Issue 12, pp. 1716 - 1725
The stereochemical course of monoterpene synthase reactions is thought to be determined early in the reaction sequence by selective binding of distinct...
NERYL PYROPHOSPHATE | ENZYMATIC CONVERSION | BIOSYNTHESIS | DIPHOSPHATE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MONOTERPENE CYCLASES | TERPENOID CYCLASE | 2-METHYLISOBORNEOL SYNTHASE | GLANDULAR TRICHOMES | MENTHA-X-PIPERITA | PRENYL-TRANSFER-REACTION | Apoproteins - chemistry | Intramolecular Lyases - antagonists & inhibitors | Organophosphates - metabolism | Polyisoprenyl Phosphates - chemistry | Intramolecular Lyases - metabolism | Stereoisomerism | Cyclohexenes - chemistry | Crystallography, X-Ray | Citrus sinensis - chemistry | Recombinant Fusion Proteins - metabolism | Citrus sinensis - enzymology | Terpenes - chemistry | Terpenes - metabolism | Plant Proteins - chemistry | Enzyme Inhibitors - chemistry | Plant Proteins - antagonists & inhibitors | Cloning, Molecular | Escherichia coli - metabolism | Protein Domains | Plant Proteins - metabolism | Diterpenes - metabolism | Apoproteins - metabolism | Diterpenes - chemistry | Apoproteins - antagonists & inhibitors | Catalytic Domain | Gene Expression | Enzyme Inhibitors - metabolism | Protein Structure, Secondary | Models, Molecular | Enzyme Assays | Recombinant Fusion Proteins - chemistry | Polyisoprenyl Phosphates - metabolism | Plant Proteins - genetics | Cyclohexenes - metabolism | Intramolecular Lyases - genetics | Escherichia coli - genetics | Apoproteins - genetics | Recombinant Fusion Proteins - genetics | Ligands | Organophosphates - chemistry | Kinetics | Intramolecular Lyases - chemistry | Phosphates | Research | Chemical properties | Orange | Carbenes
NERYL PYROPHOSPHATE | ENZYMATIC CONVERSION | BIOSYNTHESIS | DIPHOSPHATE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MONOTERPENE CYCLASES | TERPENOID CYCLASE | 2-METHYLISOBORNEOL SYNTHASE | GLANDULAR TRICHOMES | MENTHA-X-PIPERITA | PRENYL-TRANSFER-REACTION | Apoproteins - chemistry | Intramolecular Lyases - antagonists & inhibitors | Organophosphates - metabolism | Polyisoprenyl Phosphates - chemistry | Intramolecular Lyases - metabolism | Stereoisomerism | Cyclohexenes - chemistry | Crystallography, X-Ray | Citrus sinensis - chemistry | Recombinant Fusion Proteins - metabolism | Citrus sinensis - enzymology | Terpenes - chemistry | Terpenes - metabolism | Plant Proteins - chemistry | Enzyme Inhibitors - chemistry | Plant Proteins - antagonists & inhibitors | Cloning, Molecular | Escherichia coli - metabolism | Protein Domains | Plant Proteins - metabolism | Diterpenes - metabolism | Apoproteins - metabolism | Diterpenes - chemistry | Apoproteins - antagonists & inhibitors | Catalytic Domain | Gene Expression | Enzyme Inhibitors - metabolism | Protein Structure, Secondary | Models, Molecular | Enzyme Assays | Recombinant Fusion Proteins - chemistry | Polyisoprenyl Phosphates - metabolism | Plant Proteins - genetics | Cyclohexenes - metabolism | Intramolecular Lyases - genetics | Escherichia coli - genetics | Apoproteins - genetics | Recombinant Fusion Proteins - genetics | Ligands | Organophosphates - chemistry | Kinetics | Intramolecular Lyases - chemistry | Phosphates | Research | Chemical properties | Orange | Carbenes
Journal Article
The Plant Journal, ISSN 0960-7412, 05/2008, Volume 54, Issue 4, pp. 702 - 711
Summary Plant trichomes come in a variety of shapes, sizes and cellular composition. Some types, commonly called glandular trichomes, produce large amounts of...
specialized metabolism | glandular secreting trichome | secondary metabolites | tomato | lamiaceae | biosynthetic pathways | Biosynthetic pathways | Specialized metabolism | Secondary metabolites | Lamiaceae | Glandular secreting trichome | Tomato | GUTTATION FLUID | SWEET BASIL | PELTATE GLANDS | HYPERACCUMULATOR ARABIDOPSIS-HALLERI | TOBACCO | PLANT SCIENCES | KEY ENZYME | GENE FAMILY | GLANDULAR TRICHOMES | EXPRESSION | MONOTERPENE BIOSYNTHESIS | Microscopy, Electron, Scanning | Fatty Acids - chemistry | Plant Structures - metabolism | Tobacco - metabolism | Plant Epidermis - chemistry | Plant Epidermis - ultrastructure | Plant Epidermis - metabolism | Plants - ultrastructure | Lamiaceae - chemistry | Lamiaceae - ultrastructure | Plant Structures - ultrastructure | Terpenes - chemistry | Plants - metabolism | Terpenes - metabolism | Tobacco - chemistry | Lamiaceae - metabolism | Alkaloids - metabolism | Molecular Structure | Plants - chemistry | Tobacco - ultrastructure | Fatty Acids - metabolism | Plant Structures - chemistry | Alkaloids - chemistry | Metabolites | Physiological aspects | Biochemistry | Enzymes | Ribonucleic acid--RNA | Chemical compounds | Botany
specialized metabolism | glandular secreting trichome | secondary metabolites | tomato | lamiaceae | biosynthetic pathways | Biosynthetic pathways | Specialized metabolism | Secondary metabolites | Lamiaceae | Glandular secreting trichome | Tomato | GUTTATION FLUID | SWEET BASIL | PELTATE GLANDS | HYPERACCUMULATOR ARABIDOPSIS-HALLERI | TOBACCO | PLANT SCIENCES | KEY ENZYME | GENE FAMILY | GLANDULAR TRICHOMES | EXPRESSION | MONOTERPENE BIOSYNTHESIS | Microscopy, Electron, Scanning | Fatty Acids - chemistry | Plant Structures - metabolism | Tobacco - metabolism | Plant Epidermis - chemistry | Plant Epidermis - ultrastructure | Plant Epidermis - metabolism | Plants - ultrastructure | Lamiaceae - chemistry | Lamiaceae - ultrastructure | Plant Structures - ultrastructure | Terpenes - chemistry | Plants - metabolism | Terpenes - metabolism | Tobacco - chemistry | Lamiaceae - metabolism | Alkaloids - metabolism | Molecular Structure | Plants - chemistry | Tobacco - ultrastructure | Fatty Acids - metabolism | Plant Structures - chemistry | Alkaloids - chemistry | Metabolites | Physiological aspects | Biochemistry | Enzymes | Ribonucleic acid--RNA | Chemical compounds | Botany
Journal Article
Chemistry & Biodiversity, ISSN 1612-1872, 08/2015, Volume 12, Issue 8, pp. 1172 - 1183
Stachys annua subsp. annua, well‐known in central Italy as ‘stregona annuale’, is an annual, small, slightly‐scented herb, commonly found in fields and...
Glycosidic flavonoids | Stachys annua | Trichomes | Biological activities | Essential oils | ANTIOXIDANT ACTIVITY | SECONDARY METABOLITES | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESSENTIAL OIL | COMPONENTS | CHEMISTRY, MULTIDISCIPLINARY | VULGARE | FLAVONE GLYCOSIDES | GLANDULAR TRICHOMES | ANTIMICROBIAL ACTIVITY | ACETYLATED ALLOSE | CENTRAL APENNINES | Plant Oils - pharmacology | Phytol - chemistry | Sesquiterpenes - chemistry | Antioxidants - chemistry | Oils, Volatile - chemistry | Humans | Antineoplastic Agents, Phytogenic - chemistry | Oils, Volatile - pharmacology | Sesquiterpenes, Germacrane - pharmacology | Antioxidants - pharmacology | Flowers - chemistry | Neoplasms - drug therapy | Phytol - pharmacology | Trichomes - ultrastructure | Cell Line, Tumor | Italy | Sesquiterpenes, Germacrane - chemistry | Sesquiterpenes - pharmacology | Antineoplastic Agents, Phytogenic - pharmacology | Stachys - chemistry | Plant Oils - chemistry | Trichomes - chemistry
Glycosidic flavonoids | Stachys annua | Trichomes | Biological activities | Essential oils | ANTIOXIDANT ACTIVITY | SECONDARY METABOLITES | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESSENTIAL OIL | COMPONENTS | CHEMISTRY, MULTIDISCIPLINARY | VULGARE | FLAVONE GLYCOSIDES | GLANDULAR TRICHOMES | ANTIMICROBIAL ACTIVITY | ACETYLATED ALLOSE | CENTRAL APENNINES | Plant Oils - pharmacology | Phytol - chemistry | Sesquiterpenes - chemistry | Antioxidants - chemistry | Oils, Volatile - chemistry | Humans | Antineoplastic Agents, Phytogenic - chemistry | Oils, Volatile - pharmacology | Sesquiterpenes, Germacrane - pharmacology | Antioxidants - pharmacology | Flowers - chemistry | Neoplasms - drug therapy | Phytol - pharmacology | Trichomes - ultrastructure | Cell Line, Tumor | Italy | Sesquiterpenes, Germacrane - chemistry | Sesquiterpenes - pharmacology | Antineoplastic Agents, Phytogenic - pharmacology | Stachys - chemistry | Plant Oils - chemistry | Trichomes - chemistry
Journal Article
Analytical and Bioanalytical Chemistry, ISSN 1618-2642, 1/2014, Volume 406, Issue 1, pp. 171 - 182
Cell transfer by contact printing coupled with carbon-substrate-assisted laser desorption/ionization was used to directly profile and image secondary...
Biochemistry, general | Chemistry | Analytical Chemistry | Plant specialized metabolites | Food Science | Single-cell analysis | Mass spectrometry imaging | Characterization and Evaluation of Materials | Laboratory Medicine | Environmental Monitoring/Analysis | Glandular trichomes | Plant specializedmetabolites | CHEMISTRY, ANALYTICAL | SMALL MOLECULES | BIOCHEMICAL RESEARCH METHODS | GENE-EXPRESSION | TISSUES | Plant Leaves - chemistry | Printing | Trichomes - metabolism | Flavonoids - analysis | Solanum - ultrastructure | Glucosides - analysis | Metabolome | Molecular Imaging - methods | Terpenes - analysis | Solanum - metabolism | Solanum - chemistry | Terpenes - chemistry | Plant Leaves - metabolism | Trichomes - ultrastructure | Alkaloids - analysis | Glucosides - chemistry | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Flavonoids - chemistry | Alkaloids - chemistry | Plant Leaves - ultrastructure | Trichomes - chemistry | Usage | Physiological aspects | Trichomes | Chemical properties | Research | Mass spectrometry | Plant metabolites | Methods | Metabolites | Lasers | Ionization | Imaging | Images | Desorption | Contact
Biochemistry, general | Chemistry | Analytical Chemistry | Plant specialized metabolites | Food Science | Single-cell analysis | Mass spectrometry imaging | Characterization and Evaluation of Materials | Laboratory Medicine | Environmental Monitoring/Analysis | Glandular trichomes | Plant specializedmetabolites | CHEMISTRY, ANALYTICAL | SMALL MOLECULES | BIOCHEMICAL RESEARCH METHODS | GENE-EXPRESSION | TISSUES | Plant Leaves - chemistry | Printing | Trichomes - metabolism | Flavonoids - analysis | Solanum - ultrastructure | Glucosides - analysis | Metabolome | Molecular Imaging - methods | Terpenes - analysis | Solanum - metabolism | Solanum - chemistry | Terpenes - chemistry | Plant Leaves - metabolism | Trichomes - ultrastructure | Alkaloids - analysis | Glucosides - chemistry | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Flavonoids - chemistry | Alkaloids - chemistry | Plant Leaves - ultrastructure | Trichomes - chemistry | Usage | Physiological aspects | Trichomes | Chemical properties | Research | Mass spectrometry | Plant metabolites | Methods | Metabolites | Lasers | Ionization | Imaging | Images | Desorption | Contact
Journal Article
Plant Physiology, ISSN 0032-0889, 10/2012, Volume 160, Issue 2, pp. 1120 - 1129
Plants prevent dehydration by coating their aerial, primary organs with waxes. Wax compositions frequently differ between species, organs, and developmental...
Leaves | Transpiration | WHOLE PLANT AND ECOPHYSIOLOGY | Plant cuticle | Epicuticular wax | Animal cuticle | Alkanes | Chemical composition | Waxes | Gum arabic | Alcohols | ABC TRANSPORTER | TRICHOME DEVELOPMENT | PLANT CUTICLES | PERMEABILITY | THALIANA | MYB GENE | BIOSYNTHESIS | CHEMICAL-COMPOSITION | SURFACE | LEAF CUTICULAR WAXES | PLANT SCIENCES | Arabidopsis - enzymology | Genes, Plant | Oleanolic Acid - analogs & derivatives | DNA, Complementary - genetics | Agrobacterium tumefaciens - genetics | Structure-Activity Relationship | Dehydration | Triterpenes - chemistry | Oleanolic Acid - genetics | Cloning, Molecular | Water - chemistry | Intramolecular Transferases - chemistry | Waxes - chemistry | Plant Leaves - chemistry | Plant Transpiration | Transformation, Genetic | Arabidopsis - chemistry | Intramolecular Transferases - genetics | Arabidopsis - genetics | Oleanolic Acid - chemistry | DNA, Complementary - chemistry | Waxes - analysis | Alkanes - chemistry | Plant Stomata - physiology | Agrobacterium tumefaciens - chemistry
Leaves | Transpiration | WHOLE PLANT AND ECOPHYSIOLOGY | Plant cuticle | Epicuticular wax | Animal cuticle | Alkanes | Chemical composition | Waxes | Gum arabic | Alcohols | ABC TRANSPORTER | TRICHOME DEVELOPMENT | PLANT CUTICLES | PERMEABILITY | THALIANA | MYB GENE | BIOSYNTHESIS | CHEMICAL-COMPOSITION | SURFACE | LEAF CUTICULAR WAXES | PLANT SCIENCES | Arabidopsis - enzymology | Genes, Plant | Oleanolic Acid - analogs & derivatives | DNA, Complementary - genetics | Agrobacterium tumefaciens - genetics | Structure-Activity Relationship | Dehydration | Triterpenes - chemistry | Oleanolic Acid - genetics | Cloning, Molecular | Water - chemistry | Intramolecular Transferases - chemistry | Waxes - chemistry | Plant Leaves - chemistry | Plant Transpiration | Transformation, Genetic | Arabidopsis - chemistry | Intramolecular Transferases - genetics | Arabidopsis - genetics | Oleanolic Acid - chemistry | DNA, Complementary - chemistry | Waxes - analysis | Alkanes - chemistry | Plant Stomata - physiology | Agrobacterium tumefaciens - chemistry
Journal Article
Natural Product Research, ISSN 1478-6419, 07/2018, Volume 32, Issue 13, pp. 1583 - 1589
In this work, the phytochemical analysis of Teucrium chamaedrys L. collected in Italy was reported. Eight compounds were isolated and identified by means of...
phenyl-ethanoid glycosides | glycosidic hydroquinones | Teucrium chamaedrys L | flavonoids | iridoids | Teucrium chamaedrysL | SECONDARY METABOLITES | FORSYTHOSIDE B | CHEMISTRY, MEDICINAL | PHENYLETHANOID GLYCOSIDES | POLAR FRACTION | SIBILLINI NATIONAL-PARK | POLIUM-L | ANTIMICROBIAL ACTIVITIES | BIOLOGICAL-ACTIVITY | CHEMISTRY, APPLIED | GLANDULAR TRICHOMES | NEOCLERODANE DITERPENOIDS | Plant Extracts - chemistry | Teucrium - classification | Glycosides - analysis | Magnetic Resonance Spectroscopy | Iridoid Glycosides - chemistry | Arbutin - analysis | Iridoid Glycosides - analysis | Glucosides - analysis | Caffeic Acids - chemistry | Pyrans - analysis | Arbutin - chemistry | Plant Extracts - analysis | Phenols - analysis | Pyrans - chemistry | Polyphenols - analysis | Polyphenols - chemistry | Glucosides - chemistry | Italy | Molecular Structure | Teucrium - chemistry | Caffeic Acids - analysis | Glycosides - chemistry | Phytochemicals | Nuclear magnetic resonance--NMR | Species classification | Glycosides | Polyphenols | Pharmacology | Column chromatography | Index Medicus
phenyl-ethanoid glycosides | glycosidic hydroquinones | Teucrium chamaedrys L | flavonoids | iridoids | Teucrium chamaedrysL | SECONDARY METABOLITES | FORSYTHOSIDE B | CHEMISTRY, MEDICINAL | PHENYLETHANOID GLYCOSIDES | POLAR FRACTION | SIBILLINI NATIONAL-PARK | POLIUM-L | ANTIMICROBIAL ACTIVITIES | BIOLOGICAL-ACTIVITY | CHEMISTRY, APPLIED | GLANDULAR TRICHOMES | NEOCLERODANE DITERPENOIDS | Plant Extracts - chemistry | Teucrium - classification | Glycosides - analysis | Magnetic Resonance Spectroscopy | Iridoid Glycosides - chemistry | Arbutin - analysis | Iridoid Glycosides - analysis | Glucosides - analysis | Caffeic Acids - chemistry | Pyrans - analysis | Arbutin - chemistry | Plant Extracts - analysis | Phenols - analysis | Pyrans - chemistry | Polyphenols - analysis | Polyphenols - chemistry | Glucosides - chemistry | Italy | Molecular Structure | Teucrium - chemistry | Caffeic Acids - analysis | Glycosides - chemistry | Phytochemicals | Nuclear magnetic resonance--NMR | Species classification | Glycosides | Polyphenols | Pharmacology | Column chromatography | Index Medicus
Journal Article
Annual Review of Plant Biology, ISSN 1543-5008, 2006, Volume 57, Issue 1, pp. 405 - 430
Flavonoids are secondary metabolites that accumulate in most plant seeds and are involved in physiological functions such as dormancy or viability. This review...
Flavonols | WDR | Condensed tannins | MYB | bHLH | Proanthocyanidins | PLANT NATURAL-PRODUCTS | ARABIDOPSIS-THALIANA | proanthocyanidins | ZEA-MAYS | MYB TRANSCRIPTION FACTOR | COAT DEVELOPMENT | PHENYLPROPANOID BIOSYNTHESIS | ANTHOCYANIN BIOSYNTHESIS | PLANT SCIENCES | TRICHOME DEVELOPMENT | CIS-ACTING ELEMENTS | flavonols | EPIDERMAL-CELL FATE | condensed tannins | Flavonoids - genetics | Seeds - metabolism | Subcellular Fractions - metabolism | Flavonoids - metabolism | Gene Expression Regulation, Plant | Flavonoids | Flavones | Bioflavonoids | Phytochemistry | Genetic aspects | Chemical properties | Research
Flavonols | WDR | Condensed tannins | MYB | bHLH | Proanthocyanidins | PLANT NATURAL-PRODUCTS | ARABIDOPSIS-THALIANA | proanthocyanidins | ZEA-MAYS | MYB TRANSCRIPTION FACTOR | COAT DEVELOPMENT | PHENYLPROPANOID BIOSYNTHESIS | ANTHOCYANIN BIOSYNTHESIS | PLANT SCIENCES | TRICHOME DEVELOPMENT | CIS-ACTING ELEMENTS | flavonols | EPIDERMAL-CELL FATE | condensed tannins | Flavonoids - genetics | Seeds - metabolism | Subcellular Fractions - metabolism | Flavonoids - metabolism | Gene Expression Regulation, Plant | Flavonoids | Flavones | Bioflavonoids | Phytochemistry | Genetic aspects | Chemical properties | Research
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 6/2009, Volume 106, Issue 26, pp. 10865 - 10870
We identified a cis-prenyltransferase gene, neryl diphosphate synthase 1 (NDPS1). that is expressed in cultivated tomato (Solanum lycopersicum) cultivar M82...
Enzymes | Sesquiterpenes | Genes | Monoterpenes | Trichomes | Biosynthesis | Diphosphates | Plants | Terpenes | Chromosomes | Terpene synthases | Specialized metabolism | Plant biochemistry | Cis-prenyltransferases | Biochemical diversity | ARABIDOPSIS-THALIANA | plant biochemistry | SAGE SALVIA-OFFICINALIS | MULTIDISCIPLINARY SCIENCES | DOLICHOL BIOSYNTHESIS | specialized metabolism | cis-prenyltransferases | terpene synthases | PYROPHOSPHATE SYNTHETASE | biochemical diversity | LYCOPERSICON-ESCULENTUM | CIS-PRENYLTRANSFERASE | CDNA ISOLATION | SESQUITERPENE BIOSYNTHESIS | KEY ENZYME | BACTERIAL EXPRESSION | Diphosphates - metabolism | Polyisoprenyl Phosphates - chemistry | Gas Chromatography-Mass Spectrometry | Alkyl and Aryl Transferases - metabolism | DNA, Complementary - genetics | Molecular Sequence Data | Substrate Specificity | Lycopersicon esculentum - enzymology | Organophosphorus Compounds - metabolism | Plant Epidermis - metabolism | Hemiterpenes - metabolism | Dimethylallyltranstransferase - genetics | Alkyl and Aryl Transferases - genetics | Cloning, Molecular | Gene Expression Regulation, Plant | Lycopersicon esculentum - genetics | Molecular Structure | Plant Proteins - metabolism | Diterpenes - metabolism | Plant Epidermis - enzymology | Diterpenes - chemistry | Hemiterpenes - chemistry | Lycopersicon esculentum - metabolism | Gene Library | Organophosphorus Compounds - chemistry | Biosynthetic Pathways | Reverse Transcriptase Polymerase Chain Reaction | Polyisoprenyl Phosphates - metabolism | Sequence Analysis, DNA | Diphosphates - chemistry | Plant Proteins - genetics | Monoterpenes - metabolism | Dimethylallyltranstransferase - metabolism | Monoterpenes - analysis | Monoterpenes - chemistry | DNA, Complementary - chemistry | Kinetics | Tomatoes | Chemical properties | Research | Pyrophosphates | Biological Sciences
Enzymes | Sesquiterpenes | Genes | Monoterpenes | Trichomes | Biosynthesis | Diphosphates | Plants | Terpenes | Chromosomes | Terpene synthases | Specialized metabolism | Plant biochemistry | Cis-prenyltransferases | Biochemical diversity | ARABIDOPSIS-THALIANA | plant biochemistry | SAGE SALVIA-OFFICINALIS | MULTIDISCIPLINARY SCIENCES | DOLICHOL BIOSYNTHESIS | specialized metabolism | cis-prenyltransferases | terpene synthases | PYROPHOSPHATE SYNTHETASE | biochemical diversity | LYCOPERSICON-ESCULENTUM | CIS-PRENYLTRANSFERASE | CDNA ISOLATION | SESQUITERPENE BIOSYNTHESIS | KEY ENZYME | BACTERIAL EXPRESSION | Diphosphates - metabolism | Polyisoprenyl Phosphates - chemistry | Gas Chromatography-Mass Spectrometry | Alkyl and Aryl Transferases - metabolism | DNA, Complementary - genetics | Molecular Sequence Data | Substrate Specificity | Lycopersicon esculentum - enzymology | Organophosphorus Compounds - metabolism | Plant Epidermis - metabolism | Hemiterpenes - metabolism | Dimethylallyltranstransferase - genetics | Alkyl and Aryl Transferases - genetics | Cloning, Molecular | Gene Expression Regulation, Plant | Lycopersicon esculentum - genetics | Molecular Structure | Plant Proteins - metabolism | Diterpenes - metabolism | Plant Epidermis - enzymology | Diterpenes - chemistry | Hemiterpenes - chemistry | Lycopersicon esculentum - metabolism | Gene Library | Organophosphorus Compounds - chemistry | Biosynthetic Pathways | Reverse Transcriptase Polymerase Chain Reaction | Polyisoprenyl Phosphates - metabolism | Sequence Analysis, DNA | Diphosphates - chemistry | Plant Proteins - genetics | Monoterpenes - metabolism | Dimethylallyltranstransferase - metabolism | Monoterpenes - analysis | Monoterpenes - chemistry | DNA, Complementary - chemistry | Kinetics | Tomatoes | Chemical properties | Research | Pyrophosphates | Biological Sciences
Journal Article
Phytochemistry, ISSN 0031-9422, 08/2011, Volume 72, Issue 11-12, pp. 1371 - 1378
Vacuolar, epicuticular flavonoids and volatile compounds of aerial parts were correlated with the morphology of leaves and flowers of . ► We propose the...
Flavonoids | Apigenin C-glycoside | Phytochemistry | Morphology | Luteolin C-glycoside | Primula spectabilis | Volatile compounds | Primulaceae | Glandular trichomes | FLORAL PARTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | LEAVES | POLLEN | FRAGRANCE CHEMISTRY | MASS-SPECTROMETRY | EXUDATE FLAVONOIDS | PLANT SCIENCES | ORGANS | VERIS | LIQUID-CHROMATOGRAPHY | FLOWERS | Primula - chemistry | Quercetin - analogs & derivatives | Flavonoids - analysis | Magnetic Resonance Spectroscopy | Primula - anatomy & histology | Plant Components, Aerial - chemistry | Quercetin - analysis | Plant Epidermis - chemistry | Volatile Organic Compounds - analysis | Chromatography, High Pressure Liquid | Flavones - chemistry | Plant Components, Aerial - anatomy & histology | Apigenin - chemistry | Sesquiterpenes - analysis | Glucosides - chemistry | Monoterpenes - chemistry | Hemiterpenes - analysis | Flavonoids - isolation & purification | Pentanols - analysis | Volatile Organic Compounds - chemistry | Glycosides - chemistry | Plant Exudates - chemistry | Microscopy, Fluorescence | Isoflavones
Flavonoids | Apigenin C-glycoside | Phytochemistry | Morphology | Luteolin C-glycoside | Primula spectabilis | Volatile compounds | Primulaceae | Glandular trichomes | FLORAL PARTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | LEAVES | POLLEN | FRAGRANCE CHEMISTRY | MASS-SPECTROMETRY | EXUDATE FLAVONOIDS | PLANT SCIENCES | ORGANS | VERIS | LIQUID-CHROMATOGRAPHY | FLOWERS | Primula - chemistry | Quercetin - analogs & derivatives | Flavonoids - analysis | Magnetic Resonance Spectroscopy | Primula - anatomy & histology | Plant Components, Aerial - chemistry | Quercetin - analysis | Plant Epidermis - chemistry | Volatile Organic Compounds - analysis | Chromatography, High Pressure Liquid | Flavones - chemistry | Plant Components, Aerial - anatomy & histology | Apigenin - chemistry | Sesquiterpenes - analysis | Glucosides - chemistry | Monoterpenes - chemistry | Hemiterpenes - analysis | Flavonoids - isolation & purification | Pentanols - analysis | Volatile Organic Compounds - chemistry | Glycosides - chemistry | Plant Exudates - chemistry | Microscopy, Fluorescence | Isoflavones
Journal Article
New Phytologist, ISSN 0028-646X, 08/2009, Volume 183, Issue 3, pp. 848 - 867
Summary • The leaf surface is the contact point between plants and the environment and plays a crucial role in mediating biotic and abiotic interactions....
plant defense syndromes | water use efficiency | cuticular waxes | aldehydes | cardenolides | adaptation to arid environments | trichomes | monarch butterfly caterpillar (Danaus plexippus) | Cuticular waxes | Plant defense syndromes | Monarch butterfly caterpillar (Danaus plexippus) | Cardenolides | Trichomes | Water use efficiency | Aldehydes | Adaptation to arid environments | LEAVES | EPICUTICULAR WAX CRYSTALS | PLANT SCIENCES | EVOLUTION | CHEMICAL-COMPOSITION | DISCRETE CHARACTERS | CARBON ISOTOPE DISCRIMINATION | PLANT DEFENSE STRATEGIES | UV PHOTOPROTECTION | IN-VITRO RECONSTITUTION | Plant Leaves - chemistry | Asclepias - ultrastructure | Plant Leaves - parasitology | Quantitative Trait, Heritable | Asclepias - parasitology | Feeding Behavior | Phylogeny | Plant Epidermis - ultrastructure | Biological Evolution | Likelihood Functions | Animals | Analysis of Variance | Ecosystem | Surface Properties | Asclepias - genetics | Insecta - physiology | Asclepias - physiology | Waxes - chemistry | Plant Leaves - physiology | Plant Leaves - ultrastructure | Water use | Ecology | Evolutionary biology | Photosynthesis | Animal behavior
plant defense syndromes | water use efficiency | cuticular waxes | aldehydes | cardenolides | adaptation to arid environments | trichomes | monarch butterfly caterpillar (Danaus plexippus) | Cuticular waxes | Plant defense syndromes | Monarch butterfly caterpillar (Danaus plexippus) | Cardenolides | Trichomes | Water use efficiency | Aldehydes | Adaptation to arid environments | LEAVES | EPICUTICULAR WAX CRYSTALS | PLANT SCIENCES | EVOLUTION | CHEMICAL-COMPOSITION | DISCRETE CHARACTERS | CARBON ISOTOPE DISCRIMINATION | PLANT DEFENSE STRATEGIES | UV PHOTOPROTECTION | IN-VITRO RECONSTITUTION | Plant Leaves - chemistry | Asclepias - ultrastructure | Plant Leaves - parasitology | Quantitative Trait, Heritable | Asclepias - parasitology | Feeding Behavior | Phylogeny | Plant Epidermis - ultrastructure | Biological Evolution | Likelihood Functions | Animals | Analysis of Variance | Ecosystem | Surface Properties | Asclepias - genetics | Insecta - physiology | Asclepias - physiology | Waxes - chemistry | Plant Leaves - physiology | Plant Leaves - ultrastructure | Water use | Ecology | Evolutionary biology | Photosynthesis | Animal behavior
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2015, Volume 54, Issue 4, pp. 1298 - 1301
Leucosceptroids A and B are sesterterpenoids with potent antifeedant and antifungal activities. A more efficient gram‐scale total synthesis of leucosceptroid B...
aldol reaction | natural products | sesterterpenoids | total synthesis | cyclization | Aldol reaction | Cyclization | Natural products | Sesterterpenoids | Total synthesis | CANUM | HYDROSILYLATION | INDUCTION | TERPENOIDS | CHEMISTRY, MULTIDISCIPLINARY | ALCOHOLS | KETONES | DEFENSIVE SESTERTERPENOIDS | GLANDULAR TRICHOMES | ACCESS | Antifungal Agents - pharmacology | Colletotrichum - drug effects | Free Radicals - chemistry | Molecular Conformation | Sesterterpenes - chemistry | Crystallography, X-Ray | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Iodides - chemistry | Sesterterpenes - chemical synthesis | Alkenes - chemistry | Rhizoctonia - drug effects | Samarium - chemistry | Sesterterpenes - pharmacology | Catalysis | Aldehydes - chemistry
aldol reaction | natural products | sesterterpenoids | total synthesis | cyclization | Aldol reaction | Cyclization | Natural products | Sesterterpenoids | Total synthesis | CANUM | HYDROSILYLATION | INDUCTION | TERPENOIDS | CHEMISTRY, MULTIDISCIPLINARY | ALCOHOLS | KETONES | DEFENSIVE SESTERTERPENOIDS | GLANDULAR TRICHOMES | ACCESS | Antifungal Agents - pharmacology | Colletotrichum - drug effects | Free Radicals - chemistry | Molecular Conformation | Sesterterpenes - chemistry | Crystallography, X-Ray | Antifungal Agents - chemical synthesis | Antifungal Agents - chemistry | Iodides - chemistry | Sesterterpenes - chemical synthesis | Alkenes - chemistry | Rhizoctonia - drug effects | Samarium - chemistry | Sesterterpenes - pharmacology | Catalysis | Aldehydes - chemistry
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2012, Volume 7, Issue 7, p. e40856
We report the widespread occurrence of structurally diverse oleuropeyl glucose esters, including the new diester eucaglobulin B, localized specifically to the...
ACID | POLYBRACTEA | PHENOLIC-COMPOUNDS | MULTIDISCIPLINARY SCIENCES | LEAVES | CYPELLOCARPA | CHEMISTRY | FLAVONOL GLYCOSIDES | GLANDULAR TRICHOMES | MASS-SPECTROMETRY | EUCALYPTUS-GLOBULUS | Oils, Volatile - chemistry | Esters | Hydrolyzable Tannins - metabolism | Myrtaceae - chemistry | Eucalyptus - chemistry | Flavanones - chemistry | Myrtaceae - metabolism | Flavanones - metabolism | Hydrolyzable Tannins - chemistry | Glucose - chemistry | Monoterpenes - metabolism | Glucose - metabolism | Monoterpenes - chemistry | Cyclohexanecarboxylic Acids - metabolism | Oils, Volatile - metabolism | Eucalyptus - metabolism | Cyclohexanecarboxylic Acids - chemistry | Dextrose | Glucose | Trees | Biotechnology | Essential oils | Biosynthesis | Environmental conditions | Cavities | Eucalyptus | Chemistry | Acids | Oils & fats | Holes | Chemical composition | Herbivores | Localization | Species
ACID | POLYBRACTEA | PHENOLIC-COMPOUNDS | MULTIDISCIPLINARY SCIENCES | LEAVES | CYPELLOCARPA | CHEMISTRY | FLAVONOL GLYCOSIDES | GLANDULAR TRICHOMES | MASS-SPECTROMETRY | EUCALYPTUS-GLOBULUS | Oils, Volatile - chemistry | Esters | Hydrolyzable Tannins - metabolism | Myrtaceae - chemistry | Eucalyptus - chemistry | Flavanones - chemistry | Myrtaceae - metabolism | Flavanones - metabolism | Hydrolyzable Tannins - chemistry | Glucose - chemistry | Monoterpenes - metabolism | Glucose - metabolism | Monoterpenes - chemistry | Cyclohexanecarboxylic Acids - metabolism | Oils, Volatile - metabolism | Eucalyptus - metabolism | Cyclohexanecarboxylic Acids - chemistry | Dextrose | Glucose | Trees | Biotechnology | Essential oils | Biosynthesis | Environmental conditions | Cavities | Eucalyptus | Chemistry | Acids | Oils & fats | Holes | Chemical composition | Herbivores | Localization | Species
Journal Article
Phytochemistry Reviews, ISSN 1568-7767, 6/2018, Volume 17, Issue 3, pp. 471 - 489
The subfamily Barnadesioideae (Asteraceae) constitutes a group of spiny plants that are entirely restricted to South America and currently encompasses 92...
Life Sciences | Biochemistry, general | Flavonoids | Plant Genetics and Genomics | Chemistry/Food Science, general | Triterpenoids | Barnadesioideae | Traditional medicine | Plant Sciences | Organic Chemistry | CHUQUIRAGA-SPINOSA | ANTIINFLAMMATORY ACTIVITY | ARGENTINE PUNA | FLAVONOID CHEMISTRY | SUNFLOWER FAMILY ASTERACEAE | SESQUITERPENE LACTONE BIOSYNTHESIS | 5-METHYL COUMARINS | PLANT SCIENCES | PROSTATE-CANCER | ETHNOBOTANICAL SURVEY | GLANDULAR TRICHOMES | Medicinal plants | Usage | Medicine, Herbal | Medicine, Botanic | Lactones | Isoflavones | Profiling | Chemotaxonomy | Reproductive disorders | Inflammation | Phenolic compounds | Genera | Herbal medicine | Medicine | Organic chemistry | Phytochemicals | Sesquiterpene lactones | Phenols | Species
Life Sciences | Biochemistry, general | Flavonoids | Plant Genetics and Genomics | Chemistry/Food Science, general | Triterpenoids | Barnadesioideae | Traditional medicine | Plant Sciences | Organic Chemistry | CHUQUIRAGA-SPINOSA | ANTIINFLAMMATORY ACTIVITY | ARGENTINE PUNA | FLAVONOID CHEMISTRY | SUNFLOWER FAMILY ASTERACEAE | SESQUITERPENE LACTONE BIOSYNTHESIS | 5-METHYL COUMARINS | PLANT SCIENCES | PROSTATE-CANCER | ETHNOBOTANICAL SURVEY | GLANDULAR TRICHOMES | Medicinal plants | Usage | Medicine, Herbal | Medicine, Botanic | Lactones | Isoflavones | Profiling | Chemotaxonomy | Reproductive disorders | Inflammation | Phenolic compounds | Genera | Herbal medicine | Medicine | Organic chemistry | Phytochemicals | Sesquiterpene lactones | Phenols | Species
Journal Article