Biological and Pharmaceutical Bulletin, ISSN 0918-6158, 2009, Volume 32, Issue 1, pp. 86 - 90
2,4,2′,4′-Tetrahydroxy-3-(3-methyl-2-butenyl)-chalcone (TMBC), a naturally occurring compound from Morus nigra, modulated melanogenesis by inhibiting...
melanin biosynthesis | 2,4,2′,4′-tetrahydroxy-3-(3-methyl-2-butenyl)-chalcone | tyrosinase | melanin | Melanin biosynthesis | Melanin | Tyrosinase | MELANOGENESIS | KOJIC ACID | HUMAN MELANOCYTES | 2,4,2',4'-tetrahydroxy-3-(3-methyl-2-butenyl)-chalcone | MUSHROOM TYROSINASE | PHARMACOLOGY & PHARMACY | AGENTS | SKIN | HYDROQUINONE | PIGMENTATION | Cell Survival - drug effects | Levodopa - pharmacology | Plant Extracts - chemistry | Chalcone - chemistry | alpha-MSH - pharmacology | Plant Extracts - pharmacology | Antioxidants - pharmacology | RNA, Messenger - metabolism | Pyrones - pharmacology | Melanins - biosynthesis | Monophenol Monooxygenase - metabolism | Dose-Response Relationship, Drug | Animals | Chalcone - pharmacology | Melanoma, Experimental | Dopamine Agents - pharmacology | Cell Line, Tumor | Inhibitory Concentration 50 | Mice | Monophenol Monooxygenase - genetics | Gene Expression Regulation, Neoplastic - drug effects
melanin biosynthesis | 2,4,2′,4′-tetrahydroxy-3-(3-methyl-2-butenyl)-chalcone | tyrosinase | melanin | Melanin biosynthesis | Melanin | Tyrosinase | MELANOGENESIS | KOJIC ACID | HUMAN MELANOCYTES | 2,4,2',4'-tetrahydroxy-3-(3-methyl-2-butenyl)-chalcone | MUSHROOM TYROSINASE | PHARMACOLOGY & PHARMACY | AGENTS | SKIN | HYDROQUINONE | PIGMENTATION | Cell Survival - drug effects | Levodopa - pharmacology | Plant Extracts - chemistry | Chalcone - chemistry | alpha-MSH - pharmacology | Plant Extracts - pharmacology | Antioxidants - pharmacology | RNA, Messenger - metabolism | Pyrones - pharmacology | Melanins - biosynthesis | Monophenol Monooxygenase - metabolism | Dose-Response Relationship, Drug | Animals | Chalcone - pharmacology | Melanoma, Experimental | Dopamine Agents - pharmacology | Cell Line, Tumor | Inhibitory Concentration 50 | Mice | Monophenol Monooxygenase - genetics | Gene Expression Regulation, Neoplastic - drug effects
Journal Article
Chemosphere, ISSN 0045-6535, 08/2012, Volume 88, Issue 10, pp. 1154 - 1160
► Optimal pH and kinetic parameters of isolated laccases and soil extracts are similar. ► The laccase assay with ABTS has the lowest detection limit of 13.5 pg...
Soil | Humic compounds | Peroxidase | Michaelis constant | Tyrosinase | Laccase | OXIDATION | OXIDASE ACTIVITY | BIOCHEMICAL-CHARACTERIZATION | LIGNOCELLULOSE-DEGRADING ENZYMES | ENVIRONMENTAL SCIENCES | TYROSINASE ACTIVITY | QUERCUS-PETRAEA FOREST | DEGRADATION | PLEUROTUS-OSTREATUS | FUNGUS PYCNOPORUS-CINNABARINUS | Artifacts | Molecular Weight | Soil - chemistry | Enzyme Assays - methods | Trametes - enzymology | Kinetics | Benzopyrans - pharmacology | Humic Substances | Hydrogen-Ion Concentration | Laccase - metabolism | Mitosporic Fungi - enzymology | Measurement | Oxidases | Soils | Enzymes | Analysis | Microorganisms | Enzyme activity | Transformations | Assaying
Soil | Humic compounds | Peroxidase | Michaelis constant | Tyrosinase | Laccase | OXIDATION | OXIDASE ACTIVITY | BIOCHEMICAL-CHARACTERIZATION | LIGNOCELLULOSE-DEGRADING ENZYMES | ENVIRONMENTAL SCIENCES | TYROSINASE ACTIVITY | QUERCUS-PETRAEA FOREST | DEGRADATION | PLEUROTUS-OSTREATUS | FUNGUS PYCNOPORUS-CINNABARINUS | Artifacts | Molecular Weight | Soil - chemistry | Enzyme Assays - methods | Trametes - enzymology | Kinetics | Benzopyrans - pharmacology | Humic Substances | Hydrogen-Ion Concentration | Laccase - metabolism | Mitosporic Fungi - enzymology | Measurement | Oxidases | Soils | Enzymes | Analysis | Microorganisms | Enzyme activity | Transformations | Assaying
Journal Article
PLOS ONE, ISSN 1932-6203, 03/2014, Volume 9, Issue 3, p. e91809
Condensed tannins from Ficus virens leaves, fruit, and stem bark were isolated and their structures characterized by C-13 nuclear magnetic resonance...
SKIN PIGMENTATION | IN-VITRO | TOF MS ANALYSIS | MUSHROOM TYROSINASE | KINETICS | MULTIDISCIPLINARY SCIENCES | LEAVES | DOPAMINE | IONS | HPLC | RADICAL SCAVENGING ACTIVITY | Oxidoreductases - antagonists & inhibitors | Plant Extracts - chemistry | Plant Extracts - pharmacology | Molecular Conformation | Chelating Agents - chemistry | Models, Molecular | Substrate Specificity | Monophenol Monooxygenase - antagonists & inhibitors | Chelating Agents - pharmacology | Proanthocyanidins - chemistry | Copper - chemistry | Proanthocyanidins - pharmacology | Nuclear Magnetic Resonance, Biomolecular | Molecular Structure | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Catalysis | Ficus - chemistry | Monophenol Monooxygenase - chemistry | Polymerization | Biological products | Ionization | Mass spectrometry | Quinone | High performance liquid chromatography | Tannic acid | Procyanidins | Nuclear magnetic resonance--NMR | Enzyme activity | Molecular structure | Ecosystems | Bark | Fluorescence | Molecular docking | Fruits | Wetlands | Leaves | Quinones | Tannins | Enzymatic activity | Lasers | Education | Life sciences | Inhibition | Copper | Hydroxyl groups | Food | Spectroscopy | Enzymes | Free radicals | Ions | Mass spectroscopy | Desorption | Liquid chromatography | High-performance liquid chromatography | Quenching | Flavonoids | Phytochemicals | Molecular modelling | Inhibitors | Scientific imaging | Chelates | Tyrosinase | Nuclear magnetic resonance | NMR
SKIN PIGMENTATION | IN-VITRO | TOF MS ANALYSIS | MUSHROOM TYROSINASE | KINETICS | MULTIDISCIPLINARY SCIENCES | LEAVES | DOPAMINE | IONS | HPLC | RADICAL SCAVENGING ACTIVITY | Oxidoreductases - antagonists & inhibitors | Plant Extracts - chemistry | Plant Extracts - pharmacology | Molecular Conformation | Chelating Agents - chemistry | Models, Molecular | Substrate Specificity | Monophenol Monooxygenase - antagonists & inhibitors | Chelating Agents - pharmacology | Proanthocyanidins - chemistry | Copper - chemistry | Proanthocyanidins - pharmacology | Nuclear Magnetic Resonance, Biomolecular | Molecular Structure | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Catalysis | Ficus - chemistry | Monophenol Monooxygenase - chemistry | Polymerization | Biological products | Ionization | Mass spectrometry | Quinone | High performance liquid chromatography | Tannic acid | Procyanidins | Nuclear magnetic resonance--NMR | Enzyme activity | Molecular structure | Ecosystems | Bark | Fluorescence | Molecular docking | Fruits | Wetlands | Leaves | Quinones | Tannins | Enzymatic activity | Lasers | Education | Life sciences | Inhibition | Copper | Hydroxyl groups | Food | Spectroscopy | Enzymes | Free radicals | Ions | Mass spectroscopy | Desorption | Liquid chromatography | High-performance liquid chromatography | Quenching | Flavonoids | Phytochemicals | Molecular modelling | Inhibitors | Scientific imaging | Chelates | Tyrosinase | Nuclear magnetic resonance | NMR
Journal Article
Cancer, ISSN 0008-543X, 10/2013, Volume 119, Issue 20, pp. 3687 - 3695
BACKGROUND Uveal melanoma exhibits a high incidence of metastases; and, to date, there is no systemic therapy that clearly improves outcomes. The anticytotoxic...
cytotoxic T‐lymphocyte—associated protein 4 | absolute lymphocyte count | uveal melanoma | ipilimumab | immunotherapy | SURVIVAL | INTERLEUKIN-2 | cytotoxic T-lymphocyteassociated protein 4 | LYMPHOCYTE | TYROSINASE | STAGE-III | OCULAR MELANOMA | ONCOLOGY | IV MELANOMA | EXPERIENCE | MUTATIONS | EXPRESSION
cytotoxic T‐lymphocyte—associated protein 4 | absolute lymphocyte count | uveal melanoma | ipilimumab | immunotherapy | SURVIVAL | INTERLEUKIN-2 | cytotoxic T-lymphocyteassociated protein 4 | LYMPHOCYTE | TYROSINASE | STAGE-III | OCULAR MELANOMA | ONCOLOGY | IV MELANOMA | EXPERIENCE | MUTATIONS | EXPRESSION
Journal Article
Biotechnology for Biofuels, ISSN 1754-6834, 09/2017, Volume 10, Issue 1, pp. 212 - 8
Background: In the biorefinery utilizing lignocellulosic biomasses, lignin decomposition to value-added phenolic derivatives is a key issue, and recently...
Promiscuous activity | Sustainable lignin utilization | Guaiacyl glycerol-β-guaiacyl ether (GGE) | 4-Phenoxyphenol | Tyrosinase | OXIDATION | PATHWAYS | SPECIFICITY | Guaiacyl glycerol-beta-guaiacyl ether (GGE) | ENERGY & FUELS | RHODOCOCCUS-JOSTII RHA1 | SITE-DIRECTED MUTAGENESIS | PEROXIDASE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENZYMES | L-DOPA | AGARICUS-BISPORUS | DEGRADATION
Promiscuous activity | Sustainable lignin utilization | Guaiacyl glycerol-β-guaiacyl ether (GGE) | 4-Phenoxyphenol | Tyrosinase | OXIDATION | PATHWAYS | SPECIFICITY | Guaiacyl glycerol-beta-guaiacyl ether (GGE) | ENERGY & FUELS | RHODOCOCCUS-JOSTII RHA1 | SITE-DIRECTED MUTAGENESIS | PEROXIDASE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENZYMES | L-DOPA | AGARICUS-BISPORUS | DEGRADATION
Journal Article
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 2011, Volume 21, Issue 8, pp. 2445 - 2449
Computational structure prediction for mushroom tyrosinase and docking simulation with compounds and . In this study, we synthesized hydroxy and/or alkoxy...
Inflammation | Tyrosinase inhibitor | Docking analysis | Hyperpigmentation | Melanin biosynthesis | CHEMISTRY, MEDICINAL | CRYSTAL-STRUCTURE | CATECHOL OXIDASE | TYROSINASE | CHEMISTRY, ORGANIC | HIGHLY EFFICIENT | Catalytic Domain | Melanoma, Experimental - drug therapy | Monophenol Monooxygenase - antagonists & inhibitors | Melanins - biosynthesis | Monophenol Monooxygenase - metabolism | Animals | Computer Simulation | Benzothiazoles - chemistry | Benzothiazoles - toxicity | Cell Line, Tumor | Benzothiazoles - therapeutic use | Mice | Kinetics | Pyrones - toxicity | Agaricales - enzymology | Binding Sites
Inflammation | Tyrosinase inhibitor | Docking analysis | Hyperpigmentation | Melanin biosynthesis | CHEMISTRY, MEDICINAL | CRYSTAL-STRUCTURE | CATECHOL OXIDASE | TYROSINASE | CHEMISTRY, ORGANIC | HIGHLY EFFICIENT | Catalytic Domain | Melanoma, Experimental - drug therapy | Monophenol Monooxygenase - antagonists & inhibitors | Melanins - biosynthesis | Monophenol Monooxygenase - metabolism | Animals | Computer Simulation | Benzothiazoles - chemistry | Benzothiazoles - toxicity | Cell Line, Tumor | Benzothiazoles - therapeutic use | Mice | Kinetics | Pyrones - toxicity | Agaricales - enzymology | Binding Sites
Journal Article
Gene expression, ISSN 1052-2166, 1991, Volume 1, Issue 2, pp. 103 - 110
We have identified a common nonpathological polymorphism of the human tyrosinase gene. In Caucasians codon 402 can be either CGA (arginine) [p = .85] or CAA...
MOUSE TYROSINASE | MELANOMA | OCULOCUTANEOUS ALBINISM | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HUMAN-SKIN | DNA | MUTATION | GENETICS & HEREDITY | CDNA | MOLECULAR-BASIS | EXPRESSION | PIGMENTATION | Temperature | Codon | Ethnic Groups - genetics | Base Sequence | Humans | Molecular Sequence Data | Monophenol Monooxygenase - genetics | HeLa Cells | Kinetics | Monophenol Monooxygenase - metabolism | Polymorphism, Genetic
MOUSE TYROSINASE | MELANOMA | OCULOCUTANEOUS ALBINISM | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HUMAN-SKIN | DNA | MUTATION | GENETICS & HEREDITY | CDNA | MOLECULAR-BASIS | EXPRESSION | PIGMENTATION | Temperature | Codon | Ethnic Groups - genetics | Base Sequence | Humans | Molecular Sequence Data | Monophenol Monooxygenase - genetics | HeLa Cells | Kinetics | Monophenol Monooxygenase - metabolism | Polymorphism, Genetic
Journal Article
8.
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Melanogenesis inhibitory activity of a 7-O-9′-linked neolignan from Alpinia galanga fruit
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 12/2016, Volume 24, Issue 23, pp. 6215 - 6224
An aqueous acetone extract from the fruit of (Zingiberaceae) demonstrated inhibitory effects on melanogenesis in theophylline-stimulated murine B16 melanoma...
7-O-9′-Linked neolignan | Melanogenesis inhibitor | Galanganol D diacetate | Alpinia galanga | Phenylpropanoid | 7-O-9'-Linked neolignan | CHEMISTRY, MEDICINAL | MECHANISM | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | TYROSINASE INHIBITORS | CULTURED HUMAN MELANOCYTES | 7-O-9 '-Linked neolignan | MEDICINAL FOODSTUFFS | NITRIC-OXIDE PRODUCTION | STRUCTURAL REQUIREMENTS | BOESENBERGIA-ROTUNDA | TNF-ALPHA | MOUSE PERITONEAL-MACROPHAGES | FLOWER BUDS | Alpinia - chemistry | Gene Expression | Membrane Glycoproteins - metabolism | Oxidoreductases - metabolism | Fruit - chemistry | Lignans - chemistry | Oxidoreductases - genetics | Stereoisomerism | Melanocytes - metabolism | RNA, Messenger - metabolism | Lignans - pharmacology | Melanins - metabolism | Lignans - isolation & purification | Membrane Glycoproteins - genetics | Monophenol Monooxygenase - metabolism | Animals | Intramolecular Oxidoreductases - genetics | Melanocytes - drug effects | Cell Line, Tumor | Theophylline - pharmacology | Mice | Monophenol Monooxygenase - genetics | Intramolecular Oxidoreductases - metabolism
7-O-9′-Linked neolignan | Melanogenesis inhibitor | Galanganol D diacetate | Alpinia galanga | Phenylpropanoid | 7-O-9'-Linked neolignan | CHEMISTRY, MEDICINAL | MECHANISM | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | TYROSINASE INHIBITORS | CULTURED HUMAN MELANOCYTES | 7-O-9 '-Linked neolignan | MEDICINAL FOODSTUFFS | NITRIC-OXIDE PRODUCTION | STRUCTURAL REQUIREMENTS | BOESENBERGIA-ROTUNDA | TNF-ALPHA | MOUSE PERITONEAL-MACROPHAGES | FLOWER BUDS | Alpinia - chemistry | Gene Expression | Membrane Glycoproteins - metabolism | Oxidoreductases - metabolism | Fruit - chemistry | Lignans - chemistry | Oxidoreductases - genetics | Stereoisomerism | Melanocytes - metabolism | RNA, Messenger - metabolism | Lignans - pharmacology | Melanins - metabolism | Lignans - isolation & purification | Membrane Glycoproteins - genetics | Monophenol Monooxygenase - metabolism | Animals | Intramolecular Oxidoreductases - genetics | Melanocytes - drug effects | Cell Line, Tumor | Theophylline - pharmacology | Mice | Monophenol Monooxygenase - genetics | Intramolecular Oxidoreductases - metabolism
Journal Article
Food and Chemical Toxicology, ISSN 0278-6915, 11/2017, Volume 109, Issue Pt 2, pp. 1079 - 1085
, Asteraceae, a promising alternative for insect control such as leaf-cutting ants, have revealed repellent and insecticidal activity against . The different...
Total phenolic content | Ferric reducing antioxidant power | 2,2-Diphenyl-1-picrylhydrazyl | Tithonia diversifolia | Free radical-scavenging activity | Caffeic acid derivatives | TYROSINASE | FOOD SCIENCE & TECHNOLOGY | BIOLOGICAL-ACTIVITIES | Free radical-scavenging activity | IDENTIFICATION | SESQUITERPENE LACTONES | ATTA-CEPHALOTES | CHEMISTRY | TOXICOLOGY | INHIBITORS | ANTIFEEDANT | ASTERACEAE | CONSTITUENTS | Plant Leaves - chemistry | Caffeic Acids - isolation & purification | Plant Extracts - chemistry | Asteraceae - chemistry | Antioxidants - chemistry | Antioxidants - isolation & purification | Mass Spectrometry | Plant Extracts - isolation & purification | Caffeic Acids - chemistry | Molecular Structure | Chromatography, High Pressure Liquid | Antioxidants | Ants | Analysis | Plant metabolites | Resveratrol | Lactones | Iron compounds | Index Medicus
Total phenolic content | Ferric reducing antioxidant power | 2,2-Diphenyl-1-picrylhydrazyl | Tithonia diversifolia | Free radical-scavenging activity | Caffeic acid derivatives | TYROSINASE | FOOD SCIENCE & TECHNOLOGY | BIOLOGICAL-ACTIVITIES | Free radical-scavenging activity | IDENTIFICATION | SESQUITERPENE LACTONES | ATTA-CEPHALOTES | CHEMISTRY | TOXICOLOGY | INHIBITORS | ANTIFEEDANT | ASTERACEAE | CONSTITUENTS | Plant Leaves - chemistry | Caffeic Acids - isolation & purification | Plant Extracts - chemistry | Asteraceae - chemistry | Antioxidants - chemistry | Antioxidants - isolation & purification | Mass Spectrometry | Plant Extracts - isolation & purification | Caffeic Acids - chemistry | Molecular Structure | Chromatography, High Pressure Liquid | Antioxidants | Ants | Analysis | Plant metabolites | Resveratrol | Lactones | Iron compounds | Index Medicus
Journal Article
International Journal of Cosmetic Science, ISSN 0142-5463, 06/2016, Volume 38, Issue 3, pp. 319 - 324
Objective The seed coat of black soya bean (SCBS) contains high amount of anthocyanins and shows antioxidant and anti‐mushroom tyrosinase activities. The...
antioxidant | human tyrosinase | anthocyanins | black soya bean | Plant Extracts - pharmacology | Humans | Soybeans - embryology | Monophenol Monooxygenase - antagonists & inhibitors | Seeds - chemistry | Antioxidants - pharmacology | Anthocyanins - analysis | Anthocyanin | Antioxidants | Analysis | Genetically modified organisms | Genetic engineering | Soybean | Acetone
antioxidant | human tyrosinase | anthocyanins | black soya bean | Plant Extracts - pharmacology | Humans | Soybeans - embryology | Monophenol Monooxygenase - antagonists & inhibitors | Seeds - chemistry | Antioxidants - pharmacology | Anthocyanins - analysis | Anthocyanin | Antioxidants | Analysis | Genetically modified organisms | Genetic engineering | Soybean | Acetone
Journal Article
MedChemComm, ISSN 2040-2503, 3/2019, Volume 1, Issue 3, pp. 378 - 389
Tyrosinase plays an essential role in melanogenesis. Excess production of melanin can be a reason for hyperpigmentation skin disorders in mammals and enzymatic...
CHEMISTRY, MEDICINAL | MUSHROOM TYROSINASE | MECHANISM | SAFETY ASSESSMENT | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOLOGICAL EVALUATION | CHEMISTRY | MELANOGENESIS | KOJIC ACID | MOLECULAR DOCKING | DERIVATIVES | RATIONAL DESIGN | Food plants | Plants | Browning | Inhibitors | Reaction kinetics | Cosmetics | Skin | Kinetics | Inhibition | Hyperpigmentation | Chemical synthesis | Tyrosinase | Melanin
CHEMISTRY, MEDICINAL | MUSHROOM TYROSINASE | MECHANISM | SAFETY ASSESSMENT | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOLOGICAL EVALUATION | CHEMISTRY | MELANOGENESIS | KOJIC ACID | MOLECULAR DOCKING | DERIVATIVES | RATIONAL DESIGN | Food plants | Plants | Browning | Inhibitors | Reaction kinetics | Cosmetics | Skin | Kinetics | Inhibition | Hyperpigmentation | Chemical synthesis | Tyrosinase | Melanin
Journal Article
Food Chemistry, ISSN 0308-8146, 2009, Volume 112, Issue 3, pp. 609 - 613
The effects of α-cyano-4-hydroxycinnamic acid (HCCA) on the activity of mushroom tyrosinase have been studied. Results showed that HCCA could inhibit both the...
Mushroom tyrosinase | Monophenolase activity | Kinetics | α-Cyano-4-hydroxycinnamic acid | Diphenolase activity | Inhibition mechanism | NUTRITION & DIETETICS | FOOD SCIENCE & TECHNOLOGY | alpha-Cyano-4-hydroxycinnamic acid | CHEMISTRY, APPLIED
Mushroom tyrosinase | Monophenolase activity | Kinetics | α-Cyano-4-hydroxycinnamic acid | Diphenolase activity | Inhibition mechanism | NUTRITION & DIETETICS | FOOD SCIENCE & TECHNOLOGY | alpha-Cyano-4-hydroxycinnamic acid | CHEMISTRY, APPLIED
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2016, Volume 55, Issue 47, pp. 14728 - 14732
Fluorescence imaging of tyrosinase (a cancer biomarker) in living organisms is of great importance for biological studies. However, selective detection of...
recognition moiety | tyrosinase | analytical methods | fluorescent probes | reactive oxygen species | COMPLEX | PEROXYNITRITE | KOJIC ACID | LIVE CELLS | CHEMISTRY, MULTIDISCIPLINARY | OFF-ON PROBE | MELANOMA | OXIDASE | IN-VIVO | DOPAMINE | STRESS | Fluorescent Dyes - chemical synthesis | Fluorescent Dyes - chemistry | Optical Imaging | Reactive Oxygen Species - metabolism | Humans | Zebrafish | Monophenol Monooxygenase - metabolism | Animals | Monophenol Monooxygenase - analysis | Infrared Rays | Cell Line, Tumor | Mice | Molecular Structure | HeLa Cells | Fluorescence | Enzymes | Enzyme-linked immunosorbent assay | Investigations | Oxygen | Reactive oxygen species | Interference | I.R. radiation | Fluorescent indicators | Assaying | Design | Near infrared radiation | Imaging | Cells (biology) | Probes | Tyrosinase | Recognition | Cancer
recognition moiety | tyrosinase | analytical methods | fluorescent probes | reactive oxygen species | COMPLEX | PEROXYNITRITE | KOJIC ACID | LIVE CELLS | CHEMISTRY, MULTIDISCIPLINARY | OFF-ON PROBE | MELANOMA | OXIDASE | IN-VIVO | DOPAMINE | STRESS | Fluorescent Dyes - chemical synthesis | Fluorescent Dyes - chemistry | Optical Imaging | Reactive Oxygen Species - metabolism | Humans | Zebrafish | Monophenol Monooxygenase - metabolism | Animals | Monophenol Monooxygenase - analysis | Infrared Rays | Cell Line, Tumor | Mice | Molecular Structure | HeLa Cells | Fluorescence | Enzymes | Enzyme-linked immunosorbent assay | Investigations | Oxygen | Reactive oxygen species | Interference | I.R. radiation | Fluorescent indicators | Assaying | Design | Near infrared radiation | Imaging | Cells (biology) | Probes | Tyrosinase | Recognition | Cancer
Journal Article
14.
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Antioxidant and antityrosinase activity of mulberry ( Morus alba L.) twigs and root bark
Food and Chemical Toxicology, ISSN 0278-6915, 2011, Volume 49, Issue 4, pp. 785 - 790
The antioxidant and antityrosinase activities of the ethanolic extract of mulberry twigs (EEMT) were investigated. The results showed that EEMT exhibited...
Phenolic | Mulberry twigs | Antioxidant | Tyrosinase | Reducing activity | MECHANISM | FOOD SCIENCE & TECHNOLOGY | LEAVES | FLAVONOIDS | TOXICOLOGY | INHIBITORS | CONSTITUENTS | Plant Extracts - pharmacology | Enzyme Inhibitors - pharmacology | Monophenol Monooxygenase - antagonists & inhibitors | Antioxidants - pharmacology | Chromatography, High Pressure Liquid | Plant Bark - chemistry | Morus - chemistry
Phenolic | Mulberry twigs | Antioxidant | Tyrosinase | Reducing activity | MECHANISM | FOOD SCIENCE & TECHNOLOGY | LEAVES | FLAVONOIDS | TOXICOLOGY | INHIBITORS | CONSTITUENTS | Plant Extracts - pharmacology | Enzyme Inhibitors - pharmacology | Monophenol Monooxygenase - antagonists & inhibitors | Antioxidants - pharmacology | Chromatography, High Pressure Liquid | Plant Bark - chemistry | Morus - chemistry
Journal Article
Journal of the Science of Food and Agriculture, ISSN 0022-5142, 02/2015, Volume 95, Issue 3, pp. 635 - 642
BACKGROUND The aim of the current study was (i) to evaluate the bioactive potential of the leaf methanolic extract of Cynometra cauliflora L., along with its...
Cynometra cauliflora | α‐glucosidase inhibition | antioxidant | LC‐DAD‐ESIMS/MS | antiacetylcholinesterase | antityrosinase | α-glucosidase inhibition | Antiacetylcholinesterase | Antityrosinase | Antioxidant | LC-DAD-ESIMS/MS | glucosidase inhibition | PHENOLIC-COMPOUNDS | FOOD SCIENCE & TECHNOLOGY | OFFICINALIS L | AGRICULTURE, MULTIDISCIPLINARY | PLANTS | LC-DAD-ESIMS | CHEMISTRY, APPLIED | METHANOL EXTRACT | Plant Leaves - chemistry | Plant Extracts - chemistry | Fabaceae - chemistry | Plant Extracts - pharmacology | Enzyme Inhibitors - pharmacology | Polyphenols - pharmacology | Cholinesterase Inhibitors - analysis | Enzyme Inhibitors - analysis | Monophenol Monooxygenase - antagonists & inhibitors | Antioxidants - pharmacology | Cholinesterase Inhibitors - pharmacology | Polyphenols - analysis | Antioxidants - analysis | Acetylcholinesterase - metabolism | alpha-Glucosidases - metabolism | Antioxidants | Catechins | Enzymes | Procyanidins | Biocompatibility | Arrays | Chemical industries | Tyrosinase
Cynometra cauliflora | α‐glucosidase inhibition | antioxidant | LC‐DAD‐ESIMS/MS | antiacetylcholinesterase | antityrosinase | α-glucosidase inhibition | Antiacetylcholinesterase | Antityrosinase | Antioxidant | LC-DAD-ESIMS/MS | glucosidase inhibition | PHENOLIC-COMPOUNDS | FOOD SCIENCE & TECHNOLOGY | OFFICINALIS L | AGRICULTURE, MULTIDISCIPLINARY | PLANTS | LC-DAD-ESIMS | CHEMISTRY, APPLIED | METHANOL EXTRACT | Plant Leaves - chemistry | Plant Extracts - chemistry | Fabaceae - chemistry | Plant Extracts - pharmacology | Enzyme Inhibitors - pharmacology | Polyphenols - pharmacology | Cholinesterase Inhibitors - analysis | Enzyme Inhibitors - analysis | Monophenol Monooxygenase - antagonists & inhibitors | Antioxidants - pharmacology | Cholinesterase Inhibitors - pharmacology | Polyphenols - analysis | Antioxidants - analysis | Acetylcholinesterase - metabolism | alpha-Glucosidases - metabolism | Antioxidants | Catechins | Enzymes | Procyanidins | Biocompatibility | Arrays | Chemical industries | Tyrosinase
Journal Article