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1. Full Text Small-molecule aggregates inhibit amyloid polymerization
by Feng, Brian Y and Toyama, Brandon H and Wille, Holger and Colby, David W and Collins, Sean R and May, Barnaby C. H and Prusiner, Stanley B and Weissman, Jonathan and Shoichet, Brian K
Nature Chemical Biology, ISSN 1552-4450, 2008, Volume 4, Issue 3, pp. 197 - 199
Many amyloid inhibitors resemble molecules that form chemical aggregates, which are known to inhibit many proteins. Eight known chemical aggregators inhibited... 
FIBRIL FORMATION | YEAST | MECHANISM | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | PROMISCUOUS INHIBITORS | NEUROTOXICITY | Molecular Weight | Detergents - chemistry | Microscopy, Electron, Transmission - methods | Phthalimides - chemistry | Structure-Activity Relationship | Benzopyrans - chemistry | Saccharomyces cerevisiae - metabolism | Clioquinol - chemistry | Phthalimides - pharmacology | Flavanones - chemistry | Sensitivity and Specificity | Acetophenones - pharmacology | Molecular Structure | Prions - pharmacokinetics | beta-Lactamase Inhibitors | Benzopyrans - pharmacology | Saccharomyces cerevisiae Proteins - pharmacokinetics | Recombinant Proteins - metabolism | Prions - metabolism | Recombinant Proteins - antagonists & inhibitors | Phenolphthaleins - chemistry | Saccharomyces cerevisiae Proteins - antagonists & inhibitors | Congo Red - pharmacology | Flavanones - pharmacology | Recombinant Proteins - chemistry | Prions - chemistry | Clioquinol - pharmacology | Prions - antagonists & inhibitors | Saccharomyces cerevisiae - chemistry | Particle Size | Phenolphthaleins - pharmacology | beta-Lactamases - chemistry | Animals | Acetophenones - chemistry | Peptide Termination Factors | Mice | Congo Red - chemistry | Saccharomyces cerevisiae Proteins - chemistry | Proteins | Biochemistry | Inhibitor drugs | Molecular biology | Prions
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2. Full Text Immobilization of phenol-containing molecules on self-assembled monolayers on gold via surface chemistry
by Hwang, Hye-Jeong and Choi, Inseong and Kim, Young-Kwan and Kim, Young-Jin and Yeo, Woon-Seok
Colloids and Surfaces B: Biointerfaces, ISSN 0927-7765, 01/2019, Volume 173, pp. 164 - 170
Various phenol-containing molecules such as flavonoids have a wide range of biological effects including anticancer, antimicrobial, and anti-inflammatory... 
Immobilization | Self-assembled monolayers | Mannich reaction | Surface chemistry | Phenol-containing molecules | MATERIALS SCIENCE, BIOMATERIALS | BIOPHYSICS | CHEMISTRY, PHYSICAL | MASS-SPECTROMETRY | Gold - chemistry | Click Chemistry - methods | Naphthols - chemistry | Azides - chemistry | Cycloaddition Reaction - methods | Flavanones - chemistry | Carboxylic Acids - chemistry | Surface Properties | Phenols - chemistry | Sulfhydryl Compounds - chemistry | Molecular Structure | Carbodiimides - chemistry | Tyrosine - chemistry | Tyrosine | Enzymes | Usage | Flavonoids | Flavones | Bioflavonoids | Phenols | Research institutes
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3. Full Text Individual and combined antiparasitic effect of six plant metabolites against Leishmania amazonensis and Trypanosoma cruzi
by Sandjo, Louis P and de Moraes, Milene H and Kuete, Victor and Kamdoum, Blaise C and Ngadjui, Bonaventure T and Steindel, Mario
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 04/2016, Volume 26, Issue 7, pp. 1772 - 1775
Six plant metabolites including isobavachalcone ( ), 4-hydroxylonchocarpine ( ), and ( )-1-(2,2-dimethyl-2 -chromen-6-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one (... 
Antiparasitic effect | Secondary metabolites | Activity in combination | CHEMISTRY, MEDICINAL | NATURAL-PRODUCTS | DRUG DISCOVERY | CHALCONES | LEADS | CHEMISTRY, ORGANIC | PROTOZOAN NEGLECTED DISEASES | Chalcones - chemistry | Plant Extracts - chemistry | Plant Extracts - pharmacology | Humans | Trypanocidal Agents - chemistry | Structure-Activity Relationship | Flavanones - chemistry | Chalcones - pharmacology | Plants - chemistry | Leishmania mexicana - drug effects | Alkaloids - pharmacology | Flavanones - pharmacology | Zanthoxylum - chemistry | Antiprotozoal Agents - chemistry | Leishmaniasis, Cutaneous - drug therapy | Antiprotozoal Agents - pharmacology | Trypanocidal Agents - pharmacology | Antiparasitic Agents - pharmacology | Chagas Disease - drug therapy | Trypanosoma cruzi - drug effects | Moraceae - chemistry | Anthraquinones - pharmacology | Anthraquinones - chemistry | Alkaloids - chemistry | Antiparasitic Agents - chemistry | Rubiaceae - chemistry | Plant metabolites
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4. Full Text In silico docking and in vitro approaches towards BACE1 and cholinesterases inhibitory effect of citrus flavanones
by Lee, Seungeun and Youn, Kumju and Lim, GyuTae and Lee, Jinhyuk and Jun, Mira
Molecules, ISSN 1420-3049, 2018, Volume 23, Issue 7, p. 1509
Alzheimer's disease (AD) is the most prevalent neurodegenerative disease, distinctively characterized by senile plaques, neurofibrillary tangles, and synaptic... 
BACE1 | Citrus flavanones | In silico docking | Alzheimer’s disease | Hesperidin | Cholinesterases | OXIDATIVE STRESS | citrus flavanones | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | HESPERETIN | CHEMISTRY, MULTIDISCIPLINARY | hesperidin | IMPAIRMENT | in silico docking | LIQUID-CHROMATOGRAPHY | cholinesterases | ANTIOXIDANT | NARINGENIN | Alzheimer's disease | BRAIN | RAT PLASMA | Flavanones - isolation & purification | Humans | Cholinesterase Inhibitors - chemistry | Citrus - chemistry | Hesperidin - isolation & purification | Thermodynamics | Butyrylcholinesterase - chemistry | Flavanones - chemistry | Cholinesterase Inhibitors - isolation & purification | Protein Interaction Domains and Motifs | GPI-Linked Proteins - antagonists & inhibitors | Binding Sites | Aspartic Acid Endopeptidases - chemistry | Protein Conformation, alpha-Helical | Neuroprotective Agents - chemistry | Aspartic Acid Endopeptidases - antagonists & inhibitors | Nootropic Agents - isolation & purification | Enzyme Assays | Acetylcholinesterase - chemistry | Nootropic Agents - chemistry | Amyloid Precursor Protein Secretases - chemistry | GPI-Linked Proteins - chemistry | Neuroprotective Agents - isolation & purification | Protein Conformation, beta-Strand | Hesperidin - chemistry | Protein Binding | Molecular Docking Simulation | Amyloid Precursor Protein Secretases - antagonists & inhibitors | Kinetics | Enzymes | b-Site APP cleaving enzyme 1 | Hesperetin | Target recognition | Naringenin | Therapeutic applications | Acetylcholinesterase | Amyloid precursor protein | Molecular docking | Proteins | Neurofibrillary tangles | Inhibitors | Senile plaques | Enzyme kinetics
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5. Full Text Kinetics of glycoxidation of bovine serum albumin by methylglyoxal and glyoxal and its prevention by various compounds
by Sadowska-Bartosz, Izabela and Galiniak, Sabina and Bartosz, Grzegorz
Molecules, ISSN 1420-3049, 2014, Volume 19, Issue 4, pp. 4880 - 4896
The aim of this study was to compare several methods for measurement of bovine serum albumin (BSA) modification by glycoxidation with reactive dicarbonyl... 
Antioxidants | Methylglyoxal | Glyoxal | Kinetics | Glycation | OXIDATION | glyoxal | antioxidants | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROTEIN GLYCATION | INDUCTION | ASCORBIC-ACID | CHEMISTRY, MULTIDISCIPLINARY | glycation | methylglyoxal | ADVANCED GLYCATION | INHIBITION | PRODUCTS | ANTIOXIDANT | CHEMISTRY | kinetics | STRESS | Glyoxal - chemistry | Coumaric Acids - chemistry | Oxidation-Reduction | Ellagic Acid - chemistry | Spectrometry, Fluorescence | Genistein - chemistry | Kynurenine - chemistry | Glycosylation | Glyoxal - antagonists & inhibitors | Kynurenine - analogs & derivatives | Animals | Flavanones - chemistry | Glycation End Products, Advanced - chemistry | Cattle | Serum Albumin, Bovine - chemistry | Pyruvaldehyde - antagonists & inhibitors | Pyruvaldehyde - chemistry
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6. Full Text A new flavanone and other flavonoids from green perilla leaf extract inhibit nitric oxide production in interleukin 1β-treated hepatocytes
by Nakajima, Ayaka and Yamamoto, Yuka and Yoshinaka, Nao and Namba, Mayuri and Matsuo, Hirotaka and Okuyama, Tetsuya and Yoshigai, Emi and Okumura, Tadayoshi and Nishizawa, Mikio and Ikeya, Yukinobu
Bioscience, Biotechnology, and Biochemistry, ISSN 0916-8451, 01/2015, Volume 79, Issue 1, pp. 138 - 146
A new flavanone, shisoflavanone A (1), and several flavonoids were purified from the ethyl acetate-soluble fraction of green perilla leaves (Perilla frutescens... 
flavanone | nitric oxide | chemokine | flavone | green perilla | Chemokine | Flavanone | Flavone | Nitric oxide | Green perilla | GLYCOSIDES | ACID | BIOCHEMISTRY & MOLECULAR BIOLOGY | FOOD SCIENCE & TECHNOLOGY | LEAVES | MONOTERPENE GLUCOSIDES | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | CHEMISTRY, APPLIED | CONSTITUENTS | FRUTESCENS | Flavanones - isolation & purification | Plant Extracts - chemistry | Interleukin-1beta - pharmacology | Antioxidants - chemistry | Oxidative Stress | Rats, Wistar | Apigenin - isolation & purification | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Male | Anti-Inflammatory Agents, Non-Steroidal - isolation & purification | Flavones - chemistry | Hepatocytes - metabolism | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Apigenin - chemistry | Hepatocytes - cytology | Flavanones - chemistry | Luteolin - chemistry | Flavonoids - pharmacology | Flavones - isolation & purification | Flavones - pharmacology | Hepatocytes - drug effects | Interleukin-1beta - antagonists & inhibitors | Plant Leaves - chemistry | Nitric Oxide - biosynthesis | Nitric Oxide - antagonists & inhibitors | Flavanones - pharmacology | Perilla frutescens - chemistry | Rats | Umbelliferones - chemistry | Antioxidants - pharmacology | Luteolin - pharmacology | Umbelliferones - isolation & purification | Umbelliferones - pharmacology | Luteolin - isolation & purification | Animals | Antioxidants - isolation & purification | Flavonoids - isolation & purification | Primary Cell Culture | Flavonoids - chemistry | Apigenin - pharmacology | Index Medicus
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7. Full Text Thonningiiflavanonol A and thonningiiflavanonol B, two novel flavonoids, and other constituents of Ficus thonningii Blume (Moraceae)
by Ango, Patrick Y and Kapche, Deccaux W.F.G and Fotso, Ghislain W and Fozing, Christian D and Yeboah, Elizabeth M.O and Mapitse, Renameditswe and Demirtas, Ibrahim and Ngadjui, Bonaventure T and Yeboah, Samuel O
Zeitschrift für Naturforschung C, ISSN 0939-5075, 03/2016, Volume 71, Issue 3, pp. 65 - 71
A phytochemical study of has led to the isolation of two previously unreported compounds, thonningiiflavanonol A and thonningiiflavanonol B together with 16... 
thonningiiflavanonols A and B | antioxidant activity | Moraceae | Ficus thonningii | Thonningiiflavanonols a and b | Antioxidant activity | Flavanones - isolation & purification | Plant Extracts - chemistry | Parabens - analysis | Flavonoids - analysis | Antioxidants - chemistry | Oleanolic Acid - analogs & derivatives | Flavanones - analysis | Plant Bark - chemistry | Flavanones - chemistry | Quercetin - isolation & purification | Sitosterols - analysis | Luteolin - chemistry | Gallic Acid - analysis | Sitosterols - chemistry | Molecular Structure | Plant Stems - chemistry | Gallic Acid - analogs & derivatives | Antioxidants - analysis | Gallic Acid - chemistry | Parabens - isolation & purification | Gallic Acid - isolation & purification | Oleanolic Acid - isolation & purification | Quercetin - analogs & derivatives | Quercetin - chemistry | Magnetic Resonance Spectroscopy | Genistein - analysis | Quercetin - analysis | Sitosterols - isolation & purification | Genistein - chemistry | Genistein - isolation & purification | Oleanolic Acid - analysis | Luteolin - isolation & purification | Antioxidants - isolation & purification | Plant Roots - chemistry | Oleanolic Acid - chemistry | Luteolin - analysis | Parabens - chemistry | Flavonoids - isolation & purification | Ficus - chemistry | Flavonoids - chemistry | Flavonoids | Chemical properties | Flavones | Health aspects | Bioflavonoids
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8. Full Text Antioxidative compounds from Garcinia buchananii stem bark
by Stark, Timo D and Salger, Mathias and Frank, Oliver and Balemba, Onesmo B and Wakamatsu, Junichiro and Hofmann, Thomas
Journal of Natural Products, ISSN 0163-3864, 02/2015, Volume 78, Issue 2, pp. 234 - 240
An aqueous ethanolic extract of the stem bark of Garcinia buchananii showed strong antioxidative activity using H2O2 scavenging, oxygen radical absorbance... 
FLAVANONE-C-GLYCOSIDES | CHEMISTRY, MEDICINAL | POLYISOPRENYLATED BENZOPHENONES | HIV/AIDS OPPORTUNISTIC INFECTIONS | PIG DISTAL COLON | XANTHONES | PLANT SCIENCES | ETHERS | BIFLAVANONES | PLANTS | PHARMACOLOGY & PHARMACY | PRENYLATED BENZOYLPHLOROGLUCINOLS | EXTRACT | Biflavonoids - pharmacology | Depsides - isolation & purification | Flavanones - isolation & purification | Antioxidants - chemistry | Biflavonoids - chemistry | Lactones - pharmacology | Plant Bark - chemistry | Depsides - pharmacology | Terpenes - chemistry | Flavanones - chemistry | Garcinia - chemistry | Nuclear Magnetic Resonance, Biomolecular | Molecular Structure | Lactones - chemistry | Xanthones - chemistry | Terpenes - isolation & purification | Xanthones - isolation & purification | Lactones - isolation & purification | Flavanones - pharmacology | Tanzania | Depsides - chemistry | Antioxidants - pharmacology | Biflavonoids - isolation & purification | Antioxidants - isolation & purification | Hydrogen Peroxide - analysis
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9. Full Text Iron-binding and anti-Fenton properties of baicalein and baicalin
by Perez, Carlos A and Wei, Yibin and Guo, Maolin
Journal of Inorganic Biochemistry, ISSN 0162-0134, 2009, Volume 103, Issue 3, pp. 326 - 332
Baicalein and baicalin, the major bioactive compounds found in the Chinese herb , have been shown to be effective against cancer, bacterial infections and... 
Baicalein | Iron chelation | Antioxidant | Fenton chemistry | Baicalin | CELLS | LIPID-PEROXIDATION | SCUTELLARIAE RADIX | BIOCHEMISTRY & MOLECULAR BIOLOGY | COMPLEXES | INJURY | FLAVONOIDS | CHEMISTRY, INORGANIC & NUCLEAR | SUPPLEMENTATION | IN-VITRO | METABOLISM | LIVER | Iron - antagonists & inhibitors | Antioxidants - chemistry | Enzyme Inhibitors - metabolism | Antioxidants - metabolism | Flavanones - pharmacology | Enzyme Inhibitors - pharmacology | Antioxidants - pharmacology | Iron Chelating Agents - metabolism | Iron - metabolism | Iron Chelating Agents - chemistry | Hydrogen Peroxide - metabolism | Flavanones - chemistry | Iron Chelating Agents - pharmacology | Flavanones - metabolism | Enzyme Inhibitors - chemistry | Ferrozine - metabolism | Flavonoids - metabolism | Flavonoids - pharmacology | Phytotherapy | Binding Sites | Flavonoids - chemistry | Hydrogen Peroxide - antagonists & inhibitors | Scutellaria baicalensis - chemistry | Phosphates | Iron compounds | Bacterial infections | Radicals (Chemistry) | Analysis | Medicine, Botanic | Medicine, Herbal | Nuclear magnetic resonance
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10. Full Text Green pH/magnetic sensitive hydrogels based on pineapple peel cellulose and polyvinyl alcohol: synthesis, characterization and naringin prolonged release
by Dai, Hongjie and Zhang, Huan and Zhang, Yuhao and Ma, Liang and Zhou, Hongyuan and Yu, Yong and Guo, Ting and Huang, Huihua
Carbohydrate Polymers, ISSN 0144-8617, 04/2019, Volume 209, pp. 51 - 61
This study develops a green method to fabricate pH/magnetic sensitive hydrogels based on pineapple peel carboxymethyl cellulose (PCMC), regenerated... 
Nanocellulose | Polyvinyl alcohol | Naringin | Hydrogel | Pineapple peel | Ionic liquid | POLYMER SCIENCE | ACID | OXIDE | CHEMISTRY, ORGANIC | ELECTROSPUN | COMPOSITES | POLY(VINYL ALCOHOL) | SUPERABSORBENT HYDROGEL | IN-VITRO | REMOVAL | RESPONSIVE PROPERTIES | CHEMISTRY, APPLIED | Green Chemistry Technology | Polyvinyl Alcohol - chemistry | Cellulose - chemistry | Temperature | Flavanones - chemistry | Magnetic Phenomena | Drug Liberation | Ananas - chemistry | Ferrosoferric Oxide - chemistry | Drug Carriers - chemistry | Hydrogels - chemistry | Hydrogen-Ion Concentration | Drugs | Drug delivery systems | Analysis | Cellulose | Sulfuric acid | Vehicles
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11. Full Text The inhibitory effect of flavonoid aglycones on the metabolic activity of CYP3A4 enzyme
by Mustapíc, Darija Šaríc and Debeljak, Željko and Maleš, Željan and Bojíc, Mirza
Molecules, ISSN 1420-3049, 10/2018, Volume 23, Issue 10, p. 2553
Flavonoids are natural compounds that have been extensively studied due to their positive effects on human health. There are over 4000 flavonoids found in... 
Testosterone | Flavonoids | HPLC-DAD | CYP3A4 | ANTIOXIDANT ACTIVITY | OXIDATIVE STRESS | testosterone | ISORHAMNETIN | 3A4 | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHRYSIN | HUMAN LIVER-MICROSOMES | CHEMISTRY, MULTIDISCIPLINARY | BREAST-CANCER | IN-VITRO | TANGERETIN | HUMAN CYTOCHROME-P450 ENZYMES | flavonoids | Quercetin - analogs & derivatives | Quercetin - chemistry | Cytochrome P-450 CYP3A Inhibitors - pharmacology | Flavanones - pharmacology | Humans | Chromatography, High Pressure Liquid | Flavones - chemistry | Apigenin - chemistry | Testosterone - chemistry | Drug Interactions | Flavanones - chemistry | Quercetin - pharmacology | Cytochrome P-450 CYP3A - metabolism | Cytochrome P-450 CYP3A Inhibitors - chemistry | Cytochrome P-450 CYP3A - chemistry | Flavonoids - pharmacology | Cytochrome P-450 CYP3A - drug effects | Flavonoids - chemistry | Apigenin - pharmacology | Flavones - pharmacology
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12. Full Text ID‐CUBE direct analysis in real time high‐resolution mass spectrometry and its capabilities in the identification of phenolic components from the green leaves of Bergenia crassifolia L
by Chernetsova, Elena S and Crawford, Elizabeth A and Shikov, Alexander N and Pozharitskaya, Olga N and Makarov, Valery G and Morlock, Gertrud E
Rapid Communications in Mass Spectrometry, ISSN 0951-4198, 06/2012, Volume 26, Issue 11, pp. 1329 - 1337
RATIONALE Bergenia crassifolia is a plant widely used in herbal medicine. Its chemical composition has been little studied, and no studies using... 
DART | CHEMISTRY, ANALYTICAL | PRESSURE DESORPTION IONIZATION | RADICAL-SCAVENGING ACTIVITY | SPECTROSCOPY | BIOCHEMICAL RESEARCH METHODS | BLACK | FRITSCH | Arbutin - chemistry | Plant Leaves - chemistry | Phenols - isolation & purification | Plant Extracts - chemistry | Flavanones - chemistry | Hydroquinones - chemistry | Ellagic Acid - chemistry | Phenols - classification | Phenols - chemistry | Gallic Acid - chemistry | Mass Spectrometry - methods | Saxifragaceae - chemistry | Analytical chemistry | Mass spectrometry | Herbal medicine | Leaves | Ion sources | Joining | Real time | Cards | Power plants
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13. Full Text Geranylated flavonoids displaying SARS-CoV papain-like protease inhibition from the fruits of Paulownia tomentosa
by Cho, Jung Keun and Curtis-Long, Marcus J and Lee, Kon Ho and Kim, Dae Wook and Ryu, Hyung Won and Yuk, Heung Joo and Park, Ki Hun
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 06/2013, Volume 21, Issue 11, pp. 3051 - 3057
A series of geranylated flavonoids – demostrated a high inhibition against SARS-CoV pain like protease. The flavonoids – were identified as new compounds and... 
SARS-CoV PLpro | Paulownia tomentosa | Geranylated flavonoids | PLpro inhibitor | PLpro | SARS-CoV | FLAVANONES | BATS | CHEMISTRY, MEDICINAL | VIRUS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | RESPIRATORY SYNDROME CORONAVIRUS | Cysteine Endopeptidases - chemistry | Plant Extracts - chemistry | Fruit - chemistry | Viral Proteins - chemistry | Magnoliopsida - chemistry | Recombinant Proteins - chemistry | Viral Proteins - antagonists & inhibitors | Antiviral Agents - chemistry | Escherichia coli - genetics | Flavonoids - isolation & purification | Kinetics | Antiviral Agents - isolation & purification | Flavonoids - chemistry | SARS Virus - enzymology | Papain | Health aspects | Severe acute respiratory syndrome | Isoflavones
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14. Full Text Using Extra Virgin Olive Oil to Cook Vegetables Enhances Polyphenol and Carotenoid Extractability: A Study Applying the sofrito Technique
by de Alvarenga, JFR and Quifer-Rada, P and Juliano, FF and Hurtado-Barroso, S and Illan, M and Torrado-Prat, X and Lamuela-Raventos, RM
MOLECULES, ISSN 1420-3049, 04/2019, Volume 24, Issue 8, p. 1555
Olive oil is the main source of fat in the Mediterranean diet and the most frequently used ingredient in Mediterranean cuisine. Cooking with olive oil has been... 
garlic | Z-ISOMERS | carotenoid isomerization | BIOACTIVE COMPOUNDS | onion | MEDITERRANEAN DIET | PHENOLIC-COMPOUNDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | IN-VITRO BIOACCESSIBILITY | phenolic compounds | matrix effect | tomato | CHEMISTRY, MULTIDISCIPLINARY | ANTIOXIDANT CAPACITY | BIOAVAILABILITY | naringenin | BETA-CAROTENE | lycopene | TOMATO SAUCE | Lycopene - analysis | Vegetables - chemistry | Cooking | Polyphenols - chemistry | Flavanones - analysis | Olive Oil - chemistry | Onions - chemistry | Garlic - chemistry | Lycopersicon esculentum - chemistry | Carotenoids - chemistry
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15. Full Text Bioactive profiles, antioxidant activities, nitrite scavenging capacities and protective effects on H2O2-injured PC12 cells of Glycyrrhiza Glabra L. Leaf and root extracts
by Dong, Yi and Zhao, Mouming and Zhao, Tiantian and Feng, Mengying and Chen, Huiping and Zhuang, Mingzhu and Lin, Lianzhu
Molecules, ISSN 1420-3049, 2014, Volume 19, Issue 7, pp. 9101 - 9113
This study compared the total flavonoid content of Glycyrrhiza glabra L. leaf and root extracts. Results suggested that the total flavonoid content in the leaf... 
Nitrite scavenging capacity | Glycyrrhiza glabra L. leaf | Tyrosinase inhibitory activity | Liquiritin | Pinocembrin | PC12 cells | ROSMARINIC ACID | TYROSINASE | CHEMISTRY, ORGANIC | tyrosinase inhibitory activity | FLAVONOIDS | IDENTIFICATION | pinocembrin | SERRA MAXIM. HARA | PROPOLIS | liquiritin | nitrite scavenging capacity | LICORICE | INHIBITORS | Free Radical Scavengers - pharmacology | Plant Leaves - chemistry | Flavanones - isolation & purification | Plant Extracts - chemistry | Glucosides - pharmacology | Free Radical Scavengers - chemistry | Plant Extracts - pharmacology | Flavanones - pharmacology | Glycyrrhiza - chemistry | Hydrogen Peroxide - pharmacology | Rats | Plant Extracts - isolation & purification | Monophenol Monooxygenase - antagonists & inhibitors | Nitrites - chemistry | Free Radical Scavengers - isolation & purification | PC12 Cells | Cell Shape - drug effects | Glucosides - isolation & purification | Animals | Flavanones - chemistry | Plant Roots - chemistry | Glucosides - chemistry | Monophenol Monooxygenase - chemistry | Cytoprotection
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16. Full Text Cytotoxic evaluation of (2s)-5,7-dihydroxy-6-prenylflavanone derivatives loaded PLGA nanoparticles against MiaPaCa-2 cells
by Andrade-Carrera, Berenice and Clares, Beatriz and Noé, Véronique and Mallandrich, Mireia and Calpena, Ana C and García, María Luisa and Garduño-Ramírez, María Luisa
Molecules, ISSN 1420-3049, 09/2017, Volume 22, Issue 9, p. 1553
The search for new alternatives for the prevention and treatment of cancer is extremely important to minimize human mortality. Natural products are an... 
Eysenhardtia | Flavanone | MiaPaCa-2 | Cytotoxic activity | DRUG | IN-VITRO | ASSAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | flavanone | FLAVONOIDS | XANTHOHUMOL | cytotoxic activity | CHEMISTRY, MULTIDISCIPLINARY | Plant Leaves - chemistry | Cell Survival - drug effects | Flavanones - isolation & purification | Plant Extracts - chemistry | Nanoparticles - chemistry | Fabaceae - chemistry | Flavanones - pharmacology | Humans | Polylactic Acid-Polyglycolic Acid Copolymer - chemistry | Plant Extracts - isolation & purification | Antineoplastic Agents - chemistry | Drug Carriers - chemistry | Particle Size | Thermodynamics | Flavanones - chemistry | Antineoplastic Agents - isolation & purification | Surface Properties | Cell Line, Tumor | Drug Liberation | Antineoplastic Agents - pharmacology | Kinetics | Pancreatic Neoplasms | Drug Screening Assays, Antitumor | Encapsulation | Drugs | Drug delivery systems | Toxicity | Cytotoxicity | Drug delivery | Derivatives | Polylactide-co-glycolide | Anticancer properties | Nanoparticles | Natural products | Pancreatic cancer | Cancer | Càncer | Mort cel·lular | Cell death
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