Biotechnology Advances, ISSN 0734-9750, 12/2015, Volume 33, Issue 8, pp. 1697 - 1714
Phytoremediation has emerged as a green, passive, solar energy driven and cost effective approach for environmental cleanup when compared to physico-chemical...
Textile dyes | Decolorization | Toxicity | Constructed wetlands | Oxidoreductive enzymes | Effluents | Phytoreactors | Phytoremediation | Metabolic fate | WASTE-WATER TREATMENT | ASPERGILLUS-OCHRACEUS NCIM-1146 | TYPHA-ANGUSTIFOLIA LINN | PSEUDOMONAS-DESMOLYTICUM NCIM-2112 | PETUNIA-GRANDIFLORA JUSS | SOLID-STATE FERMENTATION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | SACCHAROMYCES-CEREVISIAE MTCC-463 | DIAZO REACTIVE DYE | BLUMEA-MALCOLMII HOOK | PULCHELLA SWEET TRONC | Biodegradation, Environmental | Gas Chromatography-Mass Spectrometry | Asteraceae - enzymology | Rheum - chemistry | Humans | Laccase - chemistry | Rheum - enzymology | Chromatography, High Pressure Liquid | Azo Compounds - chemistry | Asteraceae - chemistry | Benzenesulfonates - chemistry | Poaceae - enzymology | Peroxidases - chemistry | Poaceae - chemistry | Textile Industry | Coloring Agents - chemistry | Oxidases | Lignin | Metabolites | Solar energy | Genetic engineering | Dye industry | Bioremediation | Biochemical oxygen demand | Degradation | Reductases | Dyes | Plants (organisms) | Biological | Textiles
Textile dyes | Decolorization | Toxicity | Constructed wetlands | Oxidoreductive enzymes | Effluents | Phytoreactors | Phytoremediation | Metabolic fate | WASTE-WATER TREATMENT | ASPERGILLUS-OCHRACEUS NCIM-1146 | TYPHA-ANGUSTIFOLIA LINN | PSEUDOMONAS-DESMOLYTICUM NCIM-2112 | PETUNIA-GRANDIFLORA JUSS | SOLID-STATE FERMENTATION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | SACCHAROMYCES-CEREVISIAE MTCC-463 | DIAZO REACTIVE DYE | BLUMEA-MALCOLMII HOOK | PULCHELLA SWEET TRONC | Biodegradation, Environmental | Gas Chromatography-Mass Spectrometry | Asteraceae - enzymology | Rheum - chemistry | Humans | Laccase - chemistry | Rheum - enzymology | Chromatography, High Pressure Liquid | Azo Compounds - chemistry | Asteraceae - chemistry | Benzenesulfonates - chemistry | Poaceae - enzymology | Peroxidases - chemistry | Poaceae - chemistry | Textile Industry | Coloring Agents - chemistry | Oxidases | Lignin | Metabolites | Solar energy | Genetic engineering | Dye industry | Bioremediation | Biochemical oxygen demand | Degradation | Reductases | Dyes | Plants (organisms) | Biological | Textiles
Journal Article
Molecules, ISSN 1420-3049, 2018, Volume 23, Issue 5, p. 1215
We investigated the estrogenic and breast cancer inhibitory activities of chemical constituents isolated from Rhei undulati Rhizoma (roots of Rheum undulatum...
Estrogen receptor | Rheum undulatum L | Hormone replacement therapy | Menopause | CELLS | estrogen receptor | E-SCREEN ASSAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | RECEPTOR | RISK | PROLIFERATION | PHYTOESTROGENS | CHEMISTRY, MULTIDISCIPLINARY | menopause | hormone replacement therapy | REPLACEMENT THERAPY | GENE-EXPRESSION | STILBENE DERIVATIVES | Plant Extracts - chemistry | Estrogens - pharmacology | Apoptosis - drug effects | Plant Extracts - pharmacology | Rheum - chemistry | Humans | Stilbenes - chemistry | Structure-Activity Relationship | Stilbenes - pharmacology | Fulvestrant - pharmacology | Estrogens - chemistry | Glucosides - chemistry | Estrogen Receptor alpha - metabolism | Female | Molecular Structure | Cell Survival - drug effects | Emodin - metabolism | Glucosides - pharmacology | Estrogen Receptor alpha - antagonists & inhibitors | Breast Neoplasms - drug therapy | Drug Synergism | Plant Roots - chemistry | Cell Line, Tumor | Anthraquinones - pharmacology | Cell Proliferation - drug effects | Anthraquinones - chemistry | Cell proliferation | Estrogens | Stagnation | Estrogen receptors | Caspase | Cytotoxicity | Breast cancer | Inflammation | Chemical compounds | Western blotting | Fulvestrant | Emodin | Proteins | Caspase-8 | Organic chemistry | Mitochondria | Constituents | Chrysophanic acid | Xenoestrogens | Breast | Viability | Aloe | Cancer | Apoptosis
Estrogen receptor | Rheum undulatum L | Hormone replacement therapy | Menopause | CELLS | estrogen receptor | E-SCREEN ASSAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | RECEPTOR | RISK | PROLIFERATION | PHYTOESTROGENS | CHEMISTRY, MULTIDISCIPLINARY | menopause | hormone replacement therapy | REPLACEMENT THERAPY | GENE-EXPRESSION | STILBENE DERIVATIVES | Plant Extracts - chemistry | Estrogens - pharmacology | Apoptosis - drug effects | Plant Extracts - pharmacology | Rheum - chemistry | Humans | Stilbenes - chemistry | Structure-Activity Relationship | Stilbenes - pharmacology | Fulvestrant - pharmacology | Estrogens - chemistry | Glucosides - chemistry | Estrogen Receptor alpha - metabolism | Female | Molecular Structure | Cell Survival - drug effects | Emodin - metabolism | Glucosides - pharmacology | Estrogen Receptor alpha - antagonists & inhibitors | Breast Neoplasms - drug therapy | Drug Synergism | Plant Roots - chemistry | Cell Line, Tumor | Anthraquinones - pharmacology | Cell Proliferation - drug effects | Anthraquinones - chemistry | Cell proliferation | Estrogens | Stagnation | Estrogen receptors | Caspase | Cytotoxicity | Breast cancer | Inflammation | Chemical compounds | Western blotting | Fulvestrant | Emodin | Proteins | Caspase-8 | Organic chemistry | Mitochondria | Constituents | Chrysophanic acid | Xenoestrogens | Breast | Viability | Aloe | Cancer | Apoptosis
Journal Article
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 12/2004, Volume 52, Issue 26, pp. 7884 - 7890
The phenolic constituents in the roots of Rheum officinale and Rubia cordifolia were identified with the aid of high-performance liquid chromatography and...
Rheum officinale | FOOD SCIENCE & TECHNOLOGY | hydroxyanthraquinones | TANNINS | Rubia cordifolia | FLAVONOIDS | anthraquinones | antioxidant activity | phenolic constituents | structure-activity relationships | AGRICULTURE, MULTIDISCIPLINARY | radical scavenging activity | CHEMISTRY, APPLIED | Rubia - chemistry | Antioxidants - chemistry | Free Radical Scavengers - chemistry | Rheum - chemistry | Tannins - chemistry | Structure-Activity Relationship | Tannins - analysis | Phenols - analysis | Gallic Acid - analysis | Plant Roots - chemistry | Anthraquinones - analysis | Anthraquinones - chemistry | Antioxidants - analysis | Gallic Acid - chemistry
Rheum officinale | FOOD SCIENCE & TECHNOLOGY | hydroxyanthraquinones | TANNINS | Rubia cordifolia | FLAVONOIDS | anthraquinones | antioxidant activity | phenolic constituents | structure-activity relationships | AGRICULTURE, MULTIDISCIPLINARY | radical scavenging activity | CHEMISTRY, APPLIED | Rubia - chemistry | Antioxidants - chemistry | Free Radical Scavengers - chemistry | Rheum - chemistry | Tannins - chemistry | Structure-Activity Relationship | Tannins - analysis | Phenols - analysis | Gallic Acid - analysis | Plant Roots - chemistry | Anthraquinones - analysis | Anthraquinones - chemistry | Antioxidants - analysis | Gallic Acid - chemistry
Journal Article
Molecules, ISSN 1420-3049, 11/2017, Volume 22, Issue 11, p. 1838
For the European Pharmacopoeia (Ph. Eur.) herbal monograph draft of Cassia angustifolia Vahl. and Cassia senna L. leaves and pods, a safety limitation of...
Anthraquinone aglycones | Emodin | Rhein | Ultra high performance liquid chromatography (UHPLC) | Chromatographic modelling | Physcion | Design of experiment (DOE) | Herbal laxatives | Aloe-emodin | Chrysophanol | aloe-emodin | rhein | chrysophanol | herbal laxatives | BIOCHEMISTRY & MOLECULAR BIOLOGY | VALIDATION | MEDICINE | UPLC METHOD | CHEMISTRY, MULTIDISCIPLINARY | emodin | ultra high performance liquid chromatography (UHPLC) | PERFORMANCE LIQUID-CHROMATOGRAPHY | GENOTOXICITY | ANTHRAQUINONES | design of experiment (DOE) | anthraquinone aglycones | chromatographic modelling | physcion | HPLC | Rhamnus - chemistry | Plant Extracts - analysis | Plant Extracts - chemistry | Aloe - chemistry | Rheum - chemistry | Senna Plant - chemistry | Monoterpenes - analysis | Monoterpenes - chemistry | Chromatography, High Pressure Liquid | Drugs | Aglycones | Bark | Mass spectroscopy | Pharmacology | Chromatography | Optimization | Herbal medicine | Anthraquinone | Chrysophanic acid | Safety engineering | Spectrum analysis | Laxatives | Drug dependence | Design of experiments | Three dimensional models | Aloe | Index Medicus
Anthraquinone aglycones | Emodin | Rhein | Ultra high performance liquid chromatography (UHPLC) | Chromatographic modelling | Physcion | Design of experiment (DOE) | Herbal laxatives | Aloe-emodin | Chrysophanol | aloe-emodin | rhein | chrysophanol | herbal laxatives | BIOCHEMISTRY & MOLECULAR BIOLOGY | VALIDATION | MEDICINE | UPLC METHOD | CHEMISTRY, MULTIDISCIPLINARY | emodin | ultra high performance liquid chromatography (UHPLC) | PERFORMANCE LIQUID-CHROMATOGRAPHY | GENOTOXICITY | ANTHRAQUINONES | design of experiment (DOE) | anthraquinone aglycones | chromatographic modelling | physcion | HPLC | Rhamnus - chemistry | Plant Extracts - analysis | Plant Extracts - chemistry | Aloe - chemistry | Rheum - chemistry | Senna Plant - chemistry | Monoterpenes - analysis | Monoterpenes - chemistry | Chromatography, High Pressure Liquid | Drugs | Aglycones | Bark | Mass spectroscopy | Pharmacology | Chromatography | Optimization | Herbal medicine | Anthraquinone | Chrysophanic acid | Safety engineering | Spectrum analysis | Laxatives | Drug dependence | Design of experiments | Three dimensional models | Aloe | Index Medicus
Journal Article
Phytochemistry, ISSN 0031-9422, 09/2015, Volume 117, pp. 456 - 461
The synthetic broad-spectrum 2-oxoglutarate oxygenase inhibitor -oxalylglycine (NOG) is found to be present as a natural product in (rhubarb) and (spinach)...
Spinach oleracea (spinach) | N-oxalylglycine | Amino acid | Oxygenases | Rheum rhabarbarum (rhubarb) | Natural product | Inhibitor | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLANT SCIENCES | Plant Leaves - chemistry | Magnetic Resonance Spectroscopy | Rheum - chemistry | Humans | Enzyme Inhibitors - pharmacology | Alanine - chemistry | Alanine - isolation & purification | Amino Acids, Dicarboxylic - pharmacology | Escherichia coli - chemistry | HEK293 Cells - chemistry | Oxygenases - antagonists & inhibitors | Enzyme Inhibitors - isolation & purification | Alanine - analogs & derivatives | Tandem Mass Spectrometry | Amino Acids, Dicarboxylic - isolation & purification | Spinacia oleracea - chemistry | Chromatography, Liquid - methods | Ketoglutaric Acids - metabolism | Amino Acids, Dicarboxylic - chemistry | Brassica - chemistry | Oxidases | Epigenetic inheritance | Chromatin | Iron compounds | Amino acids | Gene expression | Cells
Spinach oleracea (spinach) | N-oxalylglycine | Amino acid | Oxygenases | Rheum rhabarbarum (rhubarb) | Natural product | Inhibitor | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLANT SCIENCES | Plant Leaves - chemistry | Magnetic Resonance Spectroscopy | Rheum - chemistry | Humans | Enzyme Inhibitors - pharmacology | Alanine - chemistry | Alanine - isolation & purification | Amino Acids, Dicarboxylic - pharmacology | Escherichia coli - chemistry | HEK293 Cells - chemistry | Oxygenases - antagonists & inhibitors | Enzyme Inhibitors - isolation & purification | Alanine - analogs & derivatives | Tandem Mass Spectrometry | Amino Acids, Dicarboxylic - isolation & purification | Spinacia oleracea - chemistry | Chromatography, Liquid - methods | Ketoglutaric Acids - metabolism | Amino Acids, Dicarboxylic - chemistry | Brassica - chemistry | Oxidases | Epigenetic inheritance | Chromatin | Iron compounds | Amino acids | Gene expression | Cells
Journal Article
Molecules, ISSN 1420-3049, 11/2018, Volume 23, Issue 11, p. 3048
A simple and easy to handle extraction procedure based on the use of electromagnetic induction heating is described. To assess the potential, scopes, and...
Emodin | Extraction methodologies | Anthraquinone | Rheum palmatum | Electromagnetic induction heating | HPLC | anthraquinone | UNPRENYLATED PHENYLPROPANOIDS | electromagnetic induction heating | QUANTIFICATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | extraction methodologies | CHEMISTRY, MULTIDISCIPLINARY | emodin | Plant Extracts - chemistry | Electromagnetic Phenomena | Rhizome - chemistry | Heating | Rheum - chemistry | Emodin - chemistry | Chromatography, High Pressure Liquid
Emodin | Extraction methodologies | Anthraquinone | Rheum palmatum | Electromagnetic induction heating | HPLC | anthraquinone | UNPRENYLATED PHENYLPROPANOIDS | electromagnetic induction heating | QUANTIFICATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | extraction methodologies | CHEMISTRY, MULTIDISCIPLINARY | emodin | Plant Extracts - chemistry | Electromagnetic Phenomena | Rhizome - chemistry | Heating | Rheum - chemistry | Emodin - chemistry | Chromatography, High Pressure Liquid
Journal Article
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 02/2018, Volume 28, Issue 4, pp. 552 - 557
Stilbenes have been reported to be phytoestrogen compounds owing to its structural similarity to the estrogenic agent diethylstilbestrol. To find new...
Rheum undulatum Linné | Estrogenic receptor | Polygonaceae | Stilbene derivatives | Estrogenic effect | RESVERATROL | REQUIREMENTS | (-)-EPSILON-VINIFERIN | OLIGOSTILBENES | CHEMISTRY, MEDICINAL | RHUBARB | CHEMISTRY, ORGANIC | ALPHA | BETA | GLUCOSIDES | STILBENES | DERIVATIVES | Rheum undulatum Linne | Estradiol - metabolism | Rheum - chemistry | Stereoisomerism | Humans | Phytoestrogens - chemistry | Stilbenes - metabolism | Stilbenes - chemistry | Stilbenes - pharmacology | Hep G2 Cells | Estrogen Receptor beta - metabolism | Estradiol - chemistry | Phytoestrogens - isolation & purification | Estrogen Receptor alpha - genetics | Estrogen Receptor beta - genetics | Transfection | Rhizome - chemistry | Stilbenes - isolation & purification | Estrogen Receptor alpha - metabolism | Phytoestrogens - metabolism | Estradiol - pharmacology | Phytoestrogens - pharmacology | Medicinal plants | Pharmacy | Medicine, Botanic | Diethylstilbestrol | Medicine, Herbal | Derivatives (Financial instruments) | Isoflavones
Rheum undulatum Linné | Estrogenic receptor | Polygonaceae | Stilbene derivatives | Estrogenic effect | RESVERATROL | REQUIREMENTS | (-)-EPSILON-VINIFERIN | OLIGOSTILBENES | CHEMISTRY, MEDICINAL | RHUBARB | CHEMISTRY, ORGANIC | ALPHA | BETA | GLUCOSIDES | STILBENES | DERIVATIVES | Rheum undulatum Linne | Estradiol - metabolism | Rheum - chemistry | Stereoisomerism | Humans | Phytoestrogens - chemistry | Stilbenes - metabolism | Stilbenes - chemistry | Stilbenes - pharmacology | Hep G2 Cells | Estrogen Receptor beta - metabolism | Estradiol - chemistry | Phytoestrogens - isolation & purification | Estrogen Receptor alpha - genetics | Estrogen Receptor beta - genetics | Transfection | Rhizome - chemistry | Stilbenes - isolation & purification | Estrogen Receptor alpha - metabolism | Phytoestrogens - metabolism | Estradiol - pharmacology | Phytoestrogens - pharmacology | Medicinal plants | Pharmacy | Medicine, Botanic | Diethylstilbestrol | Medicine, Herbal | Derivatives (Financial instruments) | Isoflavones
Journal Article
Analytical and Bioanalytical Chemistry, ISSN 1618-2642, 5/2013, Volume 405, Issue 12, pp. 4199 - 4212
Evaluating the quality of herbal medicines by morphological features is a convenient, quick, and practical method compared with other methods that mostly...
Biochemistry, general | Chemistry | Analytical Chemistry | Secondary metabolites | Food Science | Laser microdissection | Liquid chromatography-mass spectrometry | Characterization and Evaluation of Materials | Herbal tissues | Laboratory Medicine | Environmental Monitoring/Analysis | Rheum palmatum L | CELLS | CHEMISTRY, ANALYTICAL | PHENOLIC-COMPOUNDS | BIOCHEMICAL RESEARCH METHODS | RHUBARBS | TIME | MEDICINES | MAGNETIC-RESONANCE-SPECTROSCOPY | CONSTITUENTS | ALKALOIDS | Plant Roots - metabolism | Rheum - chemistry | Laser Capture Microdissection | Chromatography, High Pressure Liquid | Drugs, Chinese Herbal - metabolism | Plant Roots - ultrastructure | Rheum - metabolism | Rheum - ultrastructure | Rhizome - chemistry | Rhizome - metabolism | Drugs, Chinese Herbal - chemistry | Mass Spectrometry | Plant Roots - chemistry | Rhizome - ultrastructure | Metabolites | Phytochemistry | Physiological aspects | Liquid chromatography | Chemical properties | Rhubarb | Research | Identification and classification | Mass spectrometry | Methods | Herbal medicine | Herbs | Profiling | Lasers | Roots
Biochemistry, general | Chemistry | Analytical Chemistry | Secondary metabolites | Food Science | Laser microdissection | Liquid chromatography-mass spectrometry | Characterization and Evaluation of Materials | Herbal tissues | Laboratory Medicine | Environmental Monitoring/Analysis | Rheum palmatum L | CELLS | CHEMISTRY, ANALYTICAL | PHENOLIC-COMPOUNDS | BIOCHEMICAL RESEARCH METHODS | RHUBARBS | TIME | MEDICINES | MAGNETIC-RESONANCE-SPECTROSCOPY | CONSTITUENTS | ALKALOIDS | Plant Roots - metabolism | Rheum - chemistry | Laser Capture Microdissection | Chromatography, High Pressure Liquid | Drugs, Chinese Herbal - metabolism | Plant Roots - ultrastructure | Rheum - metabolism | Rheum - ultrastructure | Rhizome - chemistry | Rhizome - metabolism | Drugs, Chinese Herbal - chemistry | Mass Spectrometry | Plant Roots - chemistry | Rhizome - ultrastructure | Metabolites | Phytochemistry | Physiological aspects | Liquid chromatography | Chemical properties | Rhubarb | Research | Identification and classification | Mass spectrometry | Methods | Herbal medicine | Herbs | Profiling | Lasers | Roots
Journal Article
Artificial Cells, Nanomedicine, and Biotechnology, ISSN 2169-1401, 02/2017, Volume 45, Issue 2, pp. 372 - 379
In the present study, silver nanoparticles (AgNPs) were synthesized by using aqueous root extracts of Rheum palmatum and characterized by various spectroscopic...
silver nanoparticle | SEM | Antibacterial | Rheum palmatum | XRD | green synthesis | PLANT | MATERIALS SCIENCE, BIOMATERIALS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENGINEERING, BIOMEDICAL | LINN | Plant Extracts - chemistry | Silver - pharmacology | Rheum - chemistry | Anti-Bacterial Agents - chemistry | Metal Nanoparticles - chemistry | Plant Roots - chemistry | Pseudomonas aeruginosa - growth & development | Silver - chemistry | Anti-Bacterial Agents - pharmacology | Staphylococcus aureus - growth & development | Index Medicus
silver nanoparticle | SEM | Antibacterial | Rheum palmatum | XRD | green synthesis | PLANT | MATERIALS SCIENCE, BIOMATERIALS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENGINEERING, BIOMEDICAL | LINN | Plant Extracts - chemistry | Silver - pharmacology | Rheum - chemistry | Anti-Bacterial Agents - chemistry | Metal Nanoparticles - chemistry | Plant Roots - chemistry | Pseudomonas aeruginosa - growth & development | Silver - chemistry | Anti-Bacterial Agents - pharmacology | Staphylococcus aureus - growth & development | Index Medicus
Journal Article
世界胃肠病学杂志:英文版, ISSN 1007-9327, 2017, Volume 23, Issue 7, pp. 1125 - 1138
Yīn-Chén-Hāo decoction(YCHD) is a traditional Chinese medicine formula composed of capillaris(Artemisia capillaris), gardenia(Gardenia jasminoides), and...
Effector mechanism | Yin-Chen-Hao decoction | Hepatic disease | Review | Clinical application | RAT-LIVER | ACTIVATION | SCOPARONE 6,7-DIMETHOXYCOUMARIN | NONALCOHOLIC STEATOHEPATITIS | MASS-SPECTROMETRY | PROTECTS | INHIBITION | LIVER-INJURY | PHARMACOKINETICS | ALPHA-NAPHTHYLISOTHIOCYANATE | GASTROENTEROLOGY & HEPATOLOGY | Artemisia - chemistry | Antiviral Agents - therapeutic use | Rheum - chemistry | Humans | Coumarins - chemistry | Clinical Trials as Topic | Emodin - chemistry | Fatty Liver - drug therapy | Ascites - drug therapy | Gardenia - chemistry | Animals | Iridoids - chemistry | Anti-Inflammatory Agents - therapeutic use | Liver Diseases - drug therapy | Anthraquinones - chemistry | Chlorogenic Acid - chemistry | Drugs, Chinese Herbal - therapeutic use | Plant Extracts - therapeutic use | Yīn-Chén-Hāo decoction
Effector mechanism | Yin-Chen-Hao decoction | Hepatic disease | Review | Clinical application | RAT-LIVER | ACTIVATION | SCOPARONE 6,7-DIMETHOXYCOUMARIN | NONALCOHOLIC STEATOHEPATITIS | MASS-SPECTROMETRY | PROTECTS | INHIBITION | LIVER-INJURY | PHARMACOKINETICS | ALPHA-NAPHTHYLISOTHIOCYANATE | GASTROENTEROLOGY & HEPATOLOGY | Artemisia - chemistry | Antiviral Agents - therapeutic use | Rheum - chemistry | Humans | Coumarins - chemistry | Clinical Trials as Topic | Emodin - chemistry | Fatty Liver - drug therapy | Ascites - drug therapy | Gardenia - chemistry | Animals | Iridoids - chemistry | Anti-Inflammatory Agents - therapeutic use | Liver Diseases - drug therapy | Anthraquinones - chemistry | Chlorogenic Acid - chemistry | Drugs, Chinese Herbal - therapeutic use | Plant Extracts - therapeutic use | Yīn-Chén-Hāo decoction
Journal Article
Molecules, ISSN 1420-3049, 06/2013, Volume 18, Issue 6, pp. 7093 - 7102
Two new resveratrol trimer derivatives, named rheumlhasol A (1) and rheumlhasol B (2) were isolated from the methanolic extract of roots of Rheum lhasaense A....
DPPH radical | Rheum lhasaense A J Li et P K Hsiao | Rheumlhasol B | Rheumlhasol A | Resveratrol oligomers | BIOMIMETIC SYNTHESIS | PLANT | Rheum lhasaense A. J. Li et P. K. Hsiao | resveratrol oligomers | RHUBARB | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY | rheumlhasol A | STILBENE DERIVATIVES | rheumlhasol B | CHEMISTRY, MULTIDISCIPLINARY | Plant Extracts - chemistry | Antioxidants - chemistry | Rheum - chemistry | Stereoisomerism | Plant Roots - chemistry | Stilbenes - isolation & purification | Resveratrol | Nuclear Magnetic Resonance, Biomolecular | Molecular Structure | Stilbenes - chemistry | Antioxidants - pharmacology
DPPH radical | Rheum lhasaense A J Li et P K Hsiao | Rheumlhasol B | Rheumlhasol A | Resveratrol oligomers | BIOMIMETIC SYNTHESIS | PLANT | Rheum lhasaense A. J. Li et P. K. Hsiao | resveratrol oligomers | RHUBARB | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY | rheumlhasol A | STILBENE DERIVATIVES | rheumlhasol B | CHEMISTRY, MULTIDISCIPLINARY | Plant Extracts - chemistry | Antioxidants - chemistry | Rheum - chemistry | Stereoisomerism | Plant Roots - chemistry | Stilbenes - isolation & purification | Resveratrol | Nuclear Magnetic Resonance, Biomolecular | Molecular Structure | Stilbenes - chemistry | Antioxidants - pharmacology
Journal Article
Molecules, ISSN 1420-3049, 2014, Volume 19, Issue 8, pp. 11453 - 11464
A novel dimer of piceatannol glycoside, named rheumaustralin (1) was isolated from the underground parts of the ethnomedicinal plant Rheum austral...
DPPH radical | Piceatannol dimer | Rheum austral D. Don | Rheumaustralin | RESVERATROL | piceatannol dimer | BIOCHEMISTRY & MOLECULAR BIOLOGY | rheumaustralin | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | Free Radical Scavengers - pharmacology | Plant Extracts - chemistry | Antioxidants - chemistry | Free Radical Scavengers - chemistry | Plant Extracts - pharmacology | Rheum - chemistry | Nuclear Magnetic Resonance, Biomolecular | Molecular Structure | Stilbenes - chemistry | Antioxidants - pharmacology | Stilbenes - pharmacology | Dimerization | Antioxidants | Gallic acid | Glycosides | Dimers | Spectra | Underground | Tibet | Radicals
DPPH radical | Piceatannol dimer | Rheum austral D. Don | Rheumaustralin | RESVERATROL | piceatannol dimer | BIOCHEMISTRY & MOLECULAR BIOLOGY | rheumaustralin | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | Free Radical Scavengers - pharmacology | Plant Extracts - chemistry | Antioxidants - chemistry | Free Radical Scavengers - chemistry | Plant Extracts - pharmacology | Rheum - chemistry | Nuclear Magnetic Resonance, Biomolecular | Molecular Structure | Stilbenes - chemistry | Antioxidants - pharmacology | Stilbenes - pharmacology | Dimerization | Antioxidants | Gallic acid | Glycosides | Dimers | Spectra | Underground | Tibet | Radicals
Journal Article
Molecules, ISSN 1420-3049, 03/2016, Volume 21, Issue 3, p. 298
Mercury (Hg) causes severe nephrotoxicity in subjects with excess exposure. This work attempted to identify whether a natural medicinerhubarbhas protective...
Rhubarb | Anthraquinones | Mercury | Protection | Acute renal failure | acute renal failure | rhubarb | mercury | PHENOLIC-COMPOUNDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | protection | TOXICITY | anthraquinones | CHEMISTRY, MULTIDISCIPLINARY | EXTRACT | Plant Extracts - chemistry | Acute Kidney Injury - drug therapy | Acute Kidney Injury - pathology | Rheum - chemistry | Humans | Anthraquinones - administration & dosage | Rats | Tannins - chemistry | Protective Agents - chemistry | Plant Extracts - administration & dosage | Animals | Mercuric Chloride - toxicity | Acute Kidney Injury - chemically induced | Protective Agents - administration & dosage | Anthraquinones - chemistry
Rhubarb | Anthraquinones | Mercury | Protection | Acute renal failure | acute renal failure | rhubarb | mercury | PHENOLIC-COMPOUNDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | protection | TOXICITY | anthraquinones | CHEMISTRY, MULTIDISCIPLINARY | EXTRACT | Plant Extracts - chemistry | Acute Kidney Injury - drug therapy | Acute Kidney Injury - pathology | Rheum - chemistry | Humans | Anthraquinones - administration & dosage | Rats | Tannins - chemistry | Protective Agents - chemistry | Plant Extracts - administration & dosage | Animals | Mercuric Chloride - toxicity | Acute Kidney Injury - chemically induced | Protective Agents - administration & dosage | Anthraquinones - chemistry
Journal Article
Phytochemical Analysis, ISSN 0958-0344, 03/2012, Volume 23, Issue 2, pp. 110 - 116
ABSTRACT Introduction Semen Cassiae (SC), a traditional Chinese herbal medicine for the treatment of various diseases, is known to contain active anthraquinone...
Semen Cassiae | anthraquinone | obtusifolin | Cassia obtusifolia L | HPLC‐DAD | HPLC-DAD | OBTUSIFOLIA | GLYCOSIDES | CHEMISTRY, ANALYTICAL | BIOCHEMICAL RESEARCH METHODS | CHROMATOGRAPHY | TORA | PLANT SCIENCES | SEEDS | RHEUM-EMODI | CONSTITUENTS | Reproducibility of Results | Chromatography, High Pressure Liquid - methods | Glycosides - analysis | Emodin - analogs & derivatives | Formates - chemistry | Phosphoric Acids - chemistry | Linear Models | Acetic Acid - chemistry | Emodin - chemistry | Drugs, Chinese Herbal - chemistry | Emodin - analysis | Molecular Structure | Anthraquinones - analysis | Anthraquinones - chemistry | Cassia - chemistry | Glycosides - chemistry | Drugs, Chinese Herbal - analysis
Semen Cassiae | anthraquinone | obtusifolin | Cassia obtusifolia L | HPLC‐DAD | HPLC-DAD | OBTUSIFOLIA | GLYCOSIDES | CHEMISTRY, ANALYTICAL | BIOCHEMICAL RESEARCH METHODS | CHROMATOGRAPHY | TORA | PLANT SCIENCES | SEEDS | RHEUM-EMODI | CONSTITUENTS | Reproducibility of Results | Chromatography, High Pressure Liquid - methods | Glycosides - analysis | Emodin - analogs & derivatives | Formates - chemistry | Phosphoric Acids - chemistry | Linear Models | Acetic Acid - chemistry | Emodin - chemistry | Drugs, Chinese Herbal - chemistry | Emodin - analysis | Molecular Structure | Anthraquinones - analysis | Anthraquinones - chemistry | Cassia - chemistry | Glycosides - chemistry | Drugs, Chinese Herbal - analysis
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2017, Volume 12, Issue 3, p. e0173946
Control of temperature and duration of partial carbonization for Chinese medicines have been mainly based on experience of the processors. No quantitative...
CELLULOSE PYROLYSIS | MULTIDISCIPLINARY SCIENCES | KINETIC-ANALYSIS | DECOMPOSITION | MODEL | ACTIVATION-ENERGY | THERMOGRAVIMETRY | ISOCONVERSION METHODS | Models, Chemical | Paeonia - chemistry | Differential Thermal Analysis | Drugs, Chinese Herbal - chemistry | Rheum - chemistry | Hot Temperature | Sanguisorba - chemistry | Carbon - chemistry | Carbonization | Thermal properties | Research | Chemical properties | Rhubarb | Pimpinella | Gravimetric analysis | Fourier transforms | Atmospheric models | Cellulose | Decomposition | High temperature | Engineering | Chinese medicine | Energy | Temperature effects | Dialectics | Activation energy | Food | Herbs | Modernization | Computer simulation | Traditional Chinese medicine | Conversion | Studies | Medicine | Herbal medicine | Thermal analysis | Kinetics | Processors | Methods | Pharmaceuticals
CELLULOSE PYROLYSIS | MULTIDISCIPLINARY SCIENCES | KINETIC-ANALYSIS | DECOMPOSITION | MODEL | ACTIVATION-ENERGY | THERMOGRAVIMETRY | ISOCONVERSION METHODS | Models, Chemical | Paeonia - chemistry | Differential Thermal Analysis | Drugs, Chinese Herbal - chemistry | Rheum - chemistry | Hot Temperature | Sanguisorba - chemistry | Carbon - chemistry | Carbonization | Thermal properties | Research | Chemical properties | Rhubarb | Pimpinella | Gravimetric analysis | Fourier transforms | Atmospheric models | Cellulose | Decomposition | High temperature | Engineering | Chinese medicine | Energy | Temperature effects | Dialectics | Activation energy | Food | Herbs | Modernization | Computer simulation | Traditional Chinese medicine | Conversion | Studies | Medicine | Herbal medicine | Thermal analysis | Kinetics | Processors | Methods | Pharmaceuticals
Journal Article
Journal of the American Society for Mass Spectrometry, ISSN 1044-0305, 2007, Volume 18, Issue 1, pp. 82 - 91
Rhubarb is an important herbal medicine for the treatment of constipation, inflammation, and cancer. In this study, a facile method based on liquid...
Biotechnology | Chemistry | Analytical Chemistry | Bioinformatics | Proteomics | Organic Chemistry | RESVERATROL | CHEMISTRY, ANALYTICAL | BIANTHRONES | CHEMISTRY, PHYSICAL | IDENTIFICATION | RHEI-RHIZOMA | GALLOYL | ANTHRAQUINONES | SPECTROSCOPY | ELECTROKINETIC CHROMATOGRAPHY | CAPILLARY-ELECTROPHORESIS | SEPARATION | CONSTITUENTS | Drugs, Chinese Herbal |
Biotechnology | Chemistry | Analytical Chemistry | Bioinformatics | Proteomics | Organic Chemistry | RESVERATROL | CHEMISTRY, ANALYTICAL | BIANTHRONES | CHEMISTRY, PHYSICAL | IDENTIFICATION | RHEI-RHIZOMA | GALLOYL | ANTHRAQUINONES | SPECTROSCOPY | ELECTROKINETIC CHROMATOGRAPHY | CAPILLARY-ELECTROPHORESIS | SEPARATION | CONSTITUENTS | Drugs, Chinese Herbal |