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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
Journal Article
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
Journal Article
Journal Article
Journal Article
Molecules, ISSN 1420-3049, 09/2017, Volume 22, Issue 9, p. 1553
Journal Article