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1. Full Text Semi‐preparative isolation and purification of phenolic compounds from Achyrocline satureioides (Lam) D.C. by high‐performance counter‐current chromatography
by Bianchi, Sara Elis and Kaiser, Samuel and Pittol, Vanessa and Doneda, Eduarda and De Souza, Kellen Cristhinia Borges and Bassani, Valquiria Linck
Phytochemical Analysis, ISSN 0958-0344, 03/2019, Volume 30, Issue 2, pp. 182 - 192
Introduction Phenolic compounds present in Achyrocline satureioides are known to have therapeutic benefits like antioxidant, anti‐inflammatory, and antitumour... 
HPCCC | 3‐O‐methylquercetin | bichalcone | achyrobichalcone | marcela | 3-O-methylquercetin | CHEMISTRY, ANALYTICAL | QUANTIFICATION | STABILITY | BIOCHEMICAL RESEARCH METHODS | FLAVONOIDS | PLANT SCIENCES | QUERCETIN | IN-VITRO | ANTIOXIDANT | CHALCONES | SEPARATION | Plant Extracts - chemistry | Polyphenols - isolation & purification | Quercetin - analogs & derivatives | Polyphenols - standards | Quercetin - analysis | Countercurrent Distribution - methods | Carbon-13 Magnetic Resonance Spectroscopy - methods | Proton Magnetic Resonance Spectroscopy - methods | Reference Standards | Biflavonoids - analysis | Spectrophotometry, Ultraviolet - methods | Luteolin - analysis | Achyrocline - chemistry | Antioxidants | Analysis | Polyphenols | Nuclear magnetic resonance spectroscopy | Liquid chromatography | Mass spectrometry | Isoflavones | Nuclear magnetic resonance--NMR | Aglycones | Purity | Quadrupoles | Anticancer properties | Metabolites | Direct current | Methanol | Purification | Kaempferol | Ethyl acetate | Mass spectroscopy | Inflammation | Phenolic compounds | Chromatography | Flavonoids | Quercetin | Phenols | Dichloromethane | Methylene chloride | Acetic acid
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2. Full Text Bioactive Formylated Flavonoids from Eugenia rigida: Isolation, Synthesis, and X‑ray Crystallography
by Zaki, Mohamed A and Nanayakkara, N. P. Dhammika and Hetta, Mona H and Jacob, Melissa R and Khan, Shabana I and Mohammed, Rabab and Ibrahim, Mohamed A and Samoylenko, Volodymyr and Coleman, Christina and Fronczek, Frank R and Ferreira, Daneel and Muhammad, Ilias
Journal of Natural Products, ISSN 0163-3864, 09/2016, Volume 79, Issue 9, pp. 2341 - 2349
Two new flavonoids, rac-6-formyl-5,7-dihydroxyflavanone (1) and 2′,6′-dihydroxy-4′-methoxy-3′-methylchalcone (2), together with five known derivatives,... 
CLEISTOCALYX-OPERCULATUS | PHARMACOLOGY & PHARMACY | CHEMISTRY, MEDICINAL | CIRCULAR-DICHROISM | ABSOLUTE-CONFIGURATION | PLANT SCIENCES | Chalcones - chemistry | Puerto Rico | Escherichia coli - drug effects | Humans | Molecular Conformation | Crystallography, X-Ray | Chalcones - isolation & purification | Microbial Sensitivity Tests | Candida albicans - drug effects | Eugenia - chemistry | Chalcones - pharmacology | Nuclear Magnetic Resonance, Biomolecular | Flavonoids - pharmacology | Molecular Structure | Plant Leaves - chemistry | Methicillin-Resistant Staphylococcus aureus - drug effects | Antineoplastic Agents, Phytogenic - chemistry | Pseudomonas aeruginosa - drug effects | Cryptococcus neoformans - drug effects | Mycobacterium avium Complex - drug effects | Flavanones | Flavonoids - isolation & purification | Antineoplastic Agents, Phytogenic - pharmacology | Staphylococcus aureus - drug effects | Flavonoids - chemistry | Antineoplastic Agents, Phytogenic - isolation & purification | Drug Screening Assays, Antitumor
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3. Full Text Isolation and characterization of soybean chalcone reductase cDNA, which encodes the key enzyme for the biosynthesis of 4,2′,4′-trihydroxychalcone in legumes
by Zhang, Zhuo and Fu, Yongping and Ma, Jian and Zhang, Chao and Wang, Piwu
Molecular Breeding, ISSN 1380-3743, 12/2014, Volume 34, Issue 4, pp. 2139 - 2149
In plants, phytoalexins induced by pathogen attack play an important role in disease resistance. In soybean [Glycine max L. (Merr.)], attack by pathogenic... 
Life Sciences | Plant Pathology | Biotechnology | Isoliquiritigenin | Gene cloning and characterization | Chalcone reductase | Plant Physiology | Soybean | Daidzein | Plant Sciences | Plant Genetics & Genomics | MOLECULAR CHARACTERIZATION | AGRONOMY | NATURAL-PRODUCTS | PLANT SCIENCES | HORTICULTURE | FLAVONOID BIOSYNTHESIS | LOTUS-JAPONICUS | MEDICAGO-SATIVA | PATHWAY | BIOCHEMISTRY | GENES | GENETICS & HEREDITY | TISSUES | EXPRESSION | Enzymes | Genomics | Physiological aspects | Fluorescence | Chemical properties | Glycine | High performance liquid chromatography | Isoflavones | Reductases | Soybeans | Transcription | Roots | Genomes | Biosynthesis | Catalytic activity | Chalcone synthase | Disease resistance | Inoculation | Databases | Catalysis | Chromosomes | Cultivars | Pathogens | Legumes | Plants (botany) | Phytoalexins | Liquid chromatography | Gene expression | High-performance liquid chromatography | Substrates | Tobacco | Chromosome 9 | Isoflavonoids | Reductase
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4. Full Text Mexican propolis: A source of antioxidants and anti-inflammatory compounds, and isolation of a novel chalcone and ε-caprolactone derivative
by Guzmán-Gutiérrez, Silvia Laura and Nieto-Camacho, Antonio and Castillo-Arellano, Jorge Ivan and Huerta-Salazar, Elizabeth and Hernández-Pasteur, Griselda and Silva-Miranda, Mayra and ello-Nájera, Omar Arg and Sepúlveda-Robles, Omar and Espitia, Clara Inés and Reyes-Chilpa, Ricardo
Molecules, ISSN 1420-3049, 2018, Volume 23, Issue 2, p. 334
The propolis produced by bees are used in alternative medicine for treating inflammation, and infections, presumably due to its antioxidant properties. In this... 
Red propolis | Anti-inflammatory activity | Epoxypinocembrin chalcone | Mexican propolis | Antioxidant activity | Ε-lactone | CELLS | PHENOLIC-COMPOUNDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | SONORAN PROPOLIS | epoxypinocembrin chalcone | antioxidant activity | CANCER | CHEMISTRY, MULTIDISCIPLINARY | epsilon-lactone | anti-inflammatory activity | BRAZILIAN PROPOLIS | CHEMICAL-COMPOSITION | CHEMISTRY | EXTRACTS | ANTIMICROBIAL ACTIVITY | red propolis | CONSTITUENTS | Chalcones - chemistry | Plant Extracts - chemistry | Reactive Oxygen Species | Antioxidants - chemistry | Plant Extracts - pharmacology | Cercopithecus aethiops | Caproates - chemistry | Chromatography, High Pressure Liquid | Spectrometry, Mass, Electrospray Ionization | Anti-Bacterial Agents - chemistry | Mast Cells - metabolism | Propolis - chemistry | Molecular Structure | Vero Cells | Lactones - chemistry | Peroxidase - antagonists & inhibitors | Mast Cells - immunology | Magnetic Resonance Spectroscopy | Anti-Inflammatory Agents - pharmacology | Antioxidants - pharmacology | Cell Degranulation - immunology | Mast Cells - drug effects | Animals | Anti-Inflammatory Agents - chemistry | Propolis - metabolism | Mexico | Anti-Bacterial Agents - pharmacology | Mice | Cell Degranulation - drug effects | Peroxidase - metabolism | Edema | Antiinflammatory agents | Cinnamic acid | Propolis | Hypersensitivity | Lipid peroxidation | Ethyl acetate | Inflammation | Liquid chromatography | High-performance liquid chromatography | Caffeic acid | Bees | Asthma | Antioxidants | Properties (attributes) | Acids | Alternative medicine | Bone marrow | Peroxidase | Mast cells | Acetic acid | Peroxidation | ε-lactone
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5. Full Text Isolation of monoterpene dihydrochalcones from piper montealegreanum yuncker (piperaceae)
by Alves, Harley da Silva and Vieira da Rocha, Wilma Raianny and Braz-Filho, Raimundo and Chaves, Maria Célia de Oliveira
Molecules, ISSN 1420-3049, 06/2017, Volume 22, Issue 6, p. 874
Four new compounds were isolated from the branches of Piper montealegreanum Yuncker, a shrub found in the Amazon rainforest, including two new dihydrochalcones... 
Piper | Monoterpene dihydrochalcones | Piper montealegreanum | CHEMISTRY, ORGANIC | ADDUCTS | monoterpene dihydrochalcones | MEDICINAL-PLANTS | DERIVATIVES | ADUNCUM | Chalcones - chemistry | Monoterpenes - isolation & purification | Magnetic Resonance Spectroscopy | Chlorophyll - isolation & purification | Porphyrins - chemistry | Porphyrins - isolation & purification | Chalcones - isolation & purification | Phylogeny | Piper - chemistry | Piper - classification | Chlorophyll - chemistry | Cinnamates - isolation & purification | Monoterpenes - chemistry | Molecular Structure | Plant Stems - chemistry | Cinnamates - chemistry | Liquid-Liquid Extraction - methods | Chemotaxonomy | Rainforests | Nuclear magnetic resonance--NMR | Phaeophytin | Cinnamic acid
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6. Full Text Anti-peroxyl radical quality and antibacterial properties of rooibos infusions and their pure glycosylated polyphenolic constituents
by Simpson, Madeline J and Hjelmqvist, Daisy and López-Alarcón, Camilo and Karamehmedovic, Nadja and Minehan, Thomas G and Yepremyan, Akop and Salehani, Baback and Lissi, Eduardo and Joubert, Elizabeth and Udekwu, Klas I and Alarcon, Emilio I
Molecules, ISSN 1420-3049, 09/2013, Volume 18, Issue 9, pp. 11264 - 11280
The anti-peroxyl radical quality of two aqueous rooibos infusions and solutions of their most abundant glycosylated polyphenols was evaluated using pyrogallol... 
Antioxidant capacity | ORAC indices | Rooibos infusions | Bacteria | Glycosylated polyphenols | bacteria | DIHYDROCHALCONES | TEA ASPALATHUS-LINEARIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | SCAVENGING CAPACITY | PHENOLIC CONTENT | rooibos infusions | HERBAL TEAS | CHEMISTRY, MULTIDISCIPLINARY | METHODOLOGY | antioxidant capacity | glycosylated polyphenols | PYROGALLOL RED | AQUEOUS EXTRACTS | FLUORESCEIN | Free Radical Scavengers - pharmacology | Chalcones - chemistry | Plant Extracts - chemistry | Staphylococcus epidermidis - drug effects | Free Radical Scavengers - chemistry | Plant Extracts - pharmacology | Apigenin - isolation & purification | Escherichia coli - drug effects | Rutin - pharmacology | Polyphenols - pharmacology | Chalcones - isolation & purification | Apigenin - chemistry | Microbial Sensitivity Tests | Rutin - isolation & purification | Quercetin - isolation & purification | Anti-Bacterial Agents - chemistry | Chalcones - pharmacology | Glucosides - chemistry | Flavonoids - pharmacology | Peroxides | Beverages | Polyphenols - isolation & purification | Quercetin - analogs & derivatives | Glucosides - pharmacology | Quercetin - chemistry | Aspalathus - chemistry | Plant Extracts - isolation & purification | Anti-Bacterial Agents - isolation & purification | Free Radical Scavengers - isolation & purification | Glucosides - isolation & purification | Quercetin - pharmacology | Polyphenols - chemistry | Rutin - chemistry | Anti-Bacterial Agents - pharmacology | Flavonoids - isolation & purification | Staphylococcus aureus - drug effects | Flavonoids - chemistry | Apigenin - pharmacology | Farmaceutiska vetenskaper | Mikrobiologi inom det medicinska området | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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7. Full Text Inhibition of tyrosinase activity by polyphenol compounds from Flemingia philippinensis roots
by Wang, Yan and Curtis-Long, Marcus J and Lee, Byong Won and Yuk, Heung Joo and Kim, Dae Wook and Tan, Xue Fei and Park, Ki Hun
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 02/2014, Volume 22, Issue 3, pp. 1115 - 1120
The roots of yielded potent inhibitors against both monophenolase and diphenolase actions of tyrosinase, three of which were new dihydrochalcones ( – ). is... 
Fleminchalcone | Flemingia philippinensis | Dihydrochalcone | Tyrosinase | CHEMISTRY, MEDICINAL | MUSHROOM TYROSINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | PRENYLATED FLAVONOIDS | CHEMISTRY, ORGANIC | MOGHANIA-PHILIPPINENSIS | Oxidoreductases - antagonists & inhibitors | Polyphenols - pharmacology | Monophenol Monooxygenase - antagonists & inhibitors | Chalcones - isolation & purification | Flavones - chemistry | Terpenes - pharmacology | China | Enzyme Inhibitors - chemistry | Chalcones - pharmacology | Inhibitory Concentration 50 | Flavonoids - pharmacology | Molecular Structure | Flavones - isolation & purification | Benzopyrans - pharmacology | Flavones - pharmacology | Polyphenols - isolation & purification | Plants, Medicinal - chemistry | Terpenes - isolation & purification | Fabaceae - chemistry | Enzyme Inhibitors - pharmacology | Benzopyrans - isolation & purification | Enzyme Inhibitors - isolation & purification | Plant Roots - chemistry | Polyphenols - chemistry | Flavonoids - isolation & purification | Kinetics
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8. Full Text Bioassay-guided isolation of aldose reductase inhibitors from Artemisia dracunculus
by Logendra, Sithes and Ribnicky, David M and Yang, Hui and Poulev, Alexander and Ma, Jun and Kennelly, Edward J and Raskin, Ilya
Phytochemistry, ISSN 0031-9422, 2006, Volume 67, Issue 14, pp. 1539 - 1546
Four aldose reductase inhibitors were isolated from the ethanolic extract of the shoots of . These compounds were identified as 4,5-di- -caffeoylquinic acid,... 
Davidigenin | 4,5-Di- O-caffeoylquinic acid | Aldose reductase inhibitors | Aldose reductase | Artemisia dracunculus | Asteraceae | 2′,4′-Dihydroxy-4-methoxydihydrochalcone | 6-Demethoxycapillarisin | Dihydrochalcones | Russian tarragon | 4,5-Di-O-caffeoylquinic acid | dihydrochalcones | OXIDATIVE STRESS | NON-HYDANTOIN | CAFFEOYLQUINIC ACIDS | PHENOLIC-COMPOUNDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | davidigenin | aldose reductase | 2 ',4 '-dihydroxy-4-methoxydihydrochalcone | CYNARA-SCOLYMUS L | PLANT SCIENCES | aldose reductase inhibitors | NON-CARBOXYLIC ACID | IN-VITRO | 6-demethoxycapillarisin | 4,5-di-O-caffeoylquinic acid | FIBROBLAST GROWTH-FACTOR | POTENT ORAL ACTIVITY | DIABETIC-RAT MODELS | Chalcones - chemistry | Plant Extracts - chemistry | Quinic Acid - analogs & derivatives | Aldehyde Reductase - antagonists & inhibitors | Artemisia - chemistry | Enzyme Inhibitors - pharmacology | Quinic Acid - isolation & purification | Quinic Acid - chemistry | Chalcones - isolation & purification | Enzyme Inhibitors - isolation & purification | Chromones - chemistry | Enzyme Inhibitors - chemistry | Chalcones - pharmacology | Aldehyde Reductase - metabolism | Biological Assay | Chromones - isolation & purification | Monosaccharides - pharmacology | Molecular Structure | Quinic Acid - pharmacology | Chromones - pharmacology | Monosaccharides - chemistry | Monosaccharides - isolation & purification | Sugars | Monosaccharides
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9. Full Text Activity-guided isolation of antiplasmodial dihydrochalcones and flavanones from Piper hostmannianum var. berbicense
by Portet, Bénédicte and Fabre, Nicolas and Roumy, Vincent and Gornitzka, Heinz and Bourdy, Geneviève and Chevalley, Séverine and Sauvain, Michel and Valentin, Alexis and Moulis, Claude
Phytochemistry, ISSN 0031-9422, 2007, Volume 68, Issue 9, pp. 1312 - 1320
Four dihydrochalcones were isolated from the leaves of var. with the known dihydrochalcones 2′,6′-dihydroxy-4′-methoxydihydrochalcone, adunctin E and... 
Piperaceae | Flavanones | Plasmodium falciparum | Antiplasmodial activity | Piper hostmannianum var. berbicense | Dihydrochalcones | dihydrochalcones | BENZOIC-ACID | BOESENBERGIA-PANDURATA | RED RHIZOMES | BIOCHEMISTRY & MOLECULAR BIOLOGY | antiplasmodial activity | FLAVONOIDS | flavanones | PLANT SCIENCES | IN-VITRO | Plasimodium falciparum | PLASMODIUM-FALCIPARUM | ANTIMALARIAL ACTIVITY | Piper hostmanniantun var. berbicense | MEDICINAL-PLANTS | DERIVATIVES | CONSTITUENTS | Chalcones - chemistry | Flavanones - isolation & purification | Flavanones - pharmacology | Models, Molecular | Plasmodium - drug effects | Chalcones - isolation & purification | Piper - chemistry | Antimalarials - pharmacology | Antimalarials - isolation & purification | Animals | Flavanones - chemistry | Antimalarials - chemistry | Chalcones - pharmacology | Female | Mice | Molecular Structure | Malaria - drug therapy | Malaria | Organic chemistry | Chemical Sciences
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10. Full Text HPLC analysis, Optimization of extraction conditions and biological evaluation of corylopsis coreana uyeki flos
by Seo, Ji-Hye and Kim, Jung-Eun and Shim, Jung-Hyun and Yoon, Goo and Bang, Mi-Ae and Bae, Chun-Sik and Lee, Kyung-Jin and Park, Dae-Hun and Cho, Seung-Sik
Molecules, ISSN 1420-3049, 01/2016, Volume 21, Issue 1, p. 94
A method for the separation and quantification of three flavonoids and one isocoumarin by reverse-phase high performance liquid chromatography (HPLC) has been... 
Corylopsis coreana uyeki flos | Isocoumarin | Flavonoid | Simultaneous analysis | HPLC | CANCER-CELLS | ANTIOXIDANT ACTIVITY | ANTIINFLAMMATORY ACTIVITY | CHEMISTRY, ORGANIC | SEPTIC ARTHRITIS | FLAVONOIDS | isocoumarin | QUERCETIN | IN-VITRO | BERGENIN | simultaneous analysis | STAPHYLOCOCCUS-AUREUS | flavonoid | Corylopsis coreana Uyeki flos | INFLAMMATORY MEDIATORS | Chalcones - chemistry | Plant Extracts - chemistry | Antioxidants - chemistry | Humans | Chalcones - isolation & purification | Chromatography, High Pressure Liquid | Flowers - chemistry | Isocoumarins - isolation & purification | Benzopyrans - chemistry | Chromatography, Reverse-Phase | Reference Standards | Isocoumarins - pharmacology | Quercetin - isolation & purification | Anti-Bacterial Agents - chemistry | Sensitivity and Specificity | Anti-Inflammatory Agents - isolation & purification | Flavonoids - pharmacology | Quercetin - analogs & derivatives | Solvents | Quercetin - chemistry | Ethanol | Anti-Inflammatory Agents - pharmacology | Methicillin-Resistant Staphylococcus aureus - drug effects | Hamamelidaceae - chemistry | Anti-Bacterial Agents - isolation & purification | Antioxidants - pharmacology | Calibration | Benzopyrans - isolation & purification | Methicillin-Resistant Staphylococcus aureus - growth & development | Anti-Inflammatory Agents - chemistry | Antioxidants - isolation & purification | Anti-Bacterial Agents - pharmacology | Flavonoids - isolation & purification | Flavonoids - chemistry | Isocoumarins - chemistry
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11. Full Text Preparative isolation, quantification and antioxidant activity of dihydrochalcones from Sweet Tea (Lithocarpus polystachyus Rehd.)
by Sun, Yinshi and Li, Wei and Liu, Zhengbo
Journal of Chromatography B, ISSN 1570-0232, 10/2015, Volume 1002, pp. 372 - 378
Dihydrochalcones are the main active components of Rehd. (Sweet Tea), they are directly related to the sweet tonic beverage and traditional herb. In this work,... 
Preparative separation | Quantification | Dihydrochalcone | Sweet Tea | Antioxidant activity | CHEMISTRY, ANALYTICAL | ANTIBIOTICS | LEAVES | BIOCHEMICAL RESEARCH METHODS | IDENTIFICATION | POLYPHENOLS | COUNTER-CURRENT CHROMATOGRAPHY | PURIFICATION | PHLORHIZIN | SEPARATION | Chalcones - analysis | Antioxidants - pharmacology | Chalcones - isolation & purification | Magnetic Resonance Spectroscopy | Tea - chemistry | Chalcones - pharmacology | Antioxidants | Analysis | High performance liquid chromatography
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12. Full Text Bioassay-Guided Isolation and Structure Elucidation of Fungicidal and Herbicidal Compounds from Ambrosia salsola (Asteraceae)
by Perera, Wilmer H and Meepagala, Kumudini M and Fronczek, Frank R and Cook, Daniel D and Wedge, David E and Duke, Stephen O
Molecules, ISSN 1420-3049, 2019, Volume 24, Issue 5, p. 835
The discovery of potent natural and ecofriendly pesticides is one of the focuses of the agrochemical industry, and plant species are a source of many... 
X-ray diffraction | Ambrosia salsola | Ambrosia dumosa | Fungitoxic and phytotoxic compounds | Confertin | β-Hydroxydihydrochalcones | beta-Hydroxydihydrochalcones | confertin | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLANTS | FLAVONOIDS | fungitoxic and phytotoxic compounds | CHEMISTRY, MULTIDISCIPLINARY | SESQUITERPENE LACTONES | TRANS-CHALCONE
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13. Full Text Isolation and identification of antibacterial and cytotoxic compounds from the leaves of Muntingia calabura L
by Sufian, Adila S and Ramasamy, Kalavathy and Ahmat, Norizan and Zakaria, Zainul A and Yusof, M. Izwan M
Journal of Ethnopharmacology, ISSN 0378-8741, 03/2013, Volume 146, Issue 1, pp. 198 - 204
(Elaeocarpaceae) is one of the most common roadside trees in Malaysia. Its leaves, barks, flowers and roots have been used as a folk remedy for the treatment... 
Chalcones | Antibacterial | Elaeocarpaceae | Flavones | Cytotoxic | Muntingia calabura L | ANTIINFLAMMATORY ACTIVITY | CHEMISTRY, MEDICINAL | FLAVONOIDS | COUMARINS | PLANT SCIENCES | ANTICANCER | INTEGRATIVE & COMPLEMENTARY MEDICINE | PHARMACOLOGY & PHARMACY | AGENTS | EXTRACTS | MEDICINAL-PLANTS | DERIVATIVES | CONSTITUENTS | Cell Survival - drug effects | Plant Extracts - chemistry | Gram-Positive Bacteria - drug effects | Plant Extracts - pharmacology | Humans | Plant Leaves | Microbial Sensitivity Tests | Gram-Negative Bacteria - drug effects | MCF-7 Cells | HL-60 Cells | Anti-Bacterial Agents - pharmacology | Flavonoids - isolation & purification | Flavonoids - pharmacology | Antineoplastic Agents, Phytogenic - pharmacology | Antibacterial agents
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14. Full Text Isolation and identification of cytotoxic compounds from aeschynomene fascicularis, a mayan medicinal plant
by Caamal-Fuentes, Edgar E and Peraza-Sánchez, Sergio R and Torres-Tapia, Luis W and Moo-Puc, Rosa E
Molecules, ISSN 1420-3049, 08/2015, Volume 20, Issue 8, pp. 13563 - 13574
The plant Aeschynomene fascicularis (Fabaceae) has been used in Mayan traditional medicine in the Yucatan peninsula. However, the compounds present in the... 
Flavonoids | Antiproliferative activity | Mayan medicinal plant | Cytotoxic activity | Fabaceae | APOPTOSIS | ANGELICA-KEISKEI | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHALCONE CONSTITUENT | cytotoxic activity | flavonoids | CHEMISTRY, MULTIDISCIPLINARY | antiproliferative activity | EXTRACT | Plants, Medicinal - chemistry | Fabaceae - chemistry | Humans | Antineoplastic Agents - chemistry | Cytotoxins - isolation & purification | Plant Bark - chemistry | Hep G2 Cells | Cytotoxins - pharmacology | Antineoplastic Agents - isolation & purification | Plant Roots - chemistry | Cytotoxins - chemistry | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | HeLa Cells | Drug Screening Assays, Antitumor
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15. Full Text Isolation of isoflavones from Iris kashmiriana Baker as potential anti proliferative agents targeting NF-kappaB
by Alam, Afroze and Jaiswal, Varun and Akhtar, Sohail and