Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
phenylethyl alcohol - analogs & derivatives (1087) 1087
index medicus (797) 797
phenylethyl alcohol - pharmacology (598) 598
animals (539) 539
humans (467) 467
phenylethyl alcohol - chemistry (440) 440
food science & technology (328) 328
male (318) 318
rats (298) 298
hydroxytyrosol (284) 284
biochemistry & molecular biology (279) 279
caffeic acids - pharmacology (267) 267
olive oil (262) 262
phenylethyl alcohol - metabolism (260) 260
chemistry, applied (234) 234
antioxidants - pharmacology (211) 211
oxidative stress (206) 206
pharmacology & pharmacy (199) 199
antioxidants (198) 198
caffeic acid phenethyl ester (167) 167
phenolic-compounds (163) 163
polyphenols (162) 162
phenylethyl alcohol - analysis (158) 158
agriculture, multidisciplinary (154) 154
mice (152) 152
analysis (148) 148
female (146) 146
phenylethyl alcohol - isolation & purification (139) 139
plant oils - chemistry (132) 132
tyrosol (132) 132
antioxidant (131) 131
chemistry, medicinal (124) 124
rats, wistar (124) 124
biotechnology & applied microbiology (123) 123
apoptosis (115) 115
cells (115) 115
oxidative stress - drug effects (115) 115
molecular structure (111) 111
phenylethyl alcohol - administration & dosage (109) 109
olea - chemistry (107) 107
cape (106) 106
inhibition (105) 105
antioxidants - chemistry (100) 100
caffeic acids - chemistry (99) 99
phenols (99) 99
expression (98) 98
enzymes (96) 96
in-vitro (96) 96
nutrition & dietetics (95) 95
cell line, tumor (90) 90
propolis (90) 90
toxicology (90) 90
microbiology (89) 89
antioxidant activity (88) 88
chemistry (88) 88
chromatography, high pressure liquid (87) 87
dose-response relationship, drug (87) 87
oxidation-reduction (87) 87
phenylethyl alcohol (84) 84
phenylethyl alcohol - therapeutic use (81) 81
cell biology (80) 80
metabolism (80) 80
fermentation (79) 79
rats, sprague-dawley (79) 79
virgin olive oil (77) 77
activation (76) 76
research (74) 74
esters (73) 73
apoptosis - drug effects (71) 71
kinetics (70) 70
biotechnology (68) 68
life sciences (68) 68
metabolites (68) 68
oleuropein (67) 67
oxidation (67) 67
alcohols (66) 66
chemistry, multidisciplinary (66) 66
mediterranean diet (66) 66
mass spectrometry (65) 65
lipid-peroxidation (64) 64
adult (63) 63
cell line (63) 63
oil (63) 63
inflammation (62) 62
derivatives (61) 61
phenols - analysis (61) 61
plant sciences (61) 61
identification (60) 60
phenylethyl alcohol - chemical synthesis (59) 59
research article (59) 59
biochemistry, general (58) 58
chemistry, analytical (58) 58
physiological aspects (58) 58
plant extracts - pharmacology (58) 58
cell survival - drug effects (57) 57
structure-activity relationship (57) 57
cancer (56) 56
nf-kappa-b (56) 56
phenols - chemistry (56) 56
phenylethyl alcohol - pharmacokinetics (56) 56
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1452) 1452
Chinese (31) 31
Russian (11) 11
Japanese (4) 4
German (3) 3
French (2) 2
Korean (1) 1
Slovak (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Degradation of tyrosol by a novel electro-Fenton process using pyrite as heterogeneous source of iron catalyst
by Ammar, Salah and Oturan, Mehmet A and Oturan, Nihal and Labiadh, Lazhar and Guersalli, Amor and Abdelhedi, Ridha and Brillas, Enric
Water Research, ISSN 0043-1354, 05/2015, Volume 74, pp. 77 - 87
Tyrosol (TY) is one of the most abundant phenolic components of olive oil mill wastewaters. Here, the degradation of synthetic aqueous solutions of 0.30 mM TY... 
Hydroxyl radicals | Heterogeneous catalysis | Electro-Fenton | Pyrite | Wastewater treatment | Tyrosol | AQUEOUS-MEDIUM | FELT CATHODE | WATER RESOURCES | TOXICITY | ENVIRONMENTAL SCIENCES | OIL | ADVANCED OXIDATION PROCESSES | ENGINEERING, ENVIRONMENTAL | MILL WASTE-WATER | MINERALIZATION | DOPED DIAMOND ANODE | HYDROGEN-PEROXIDE | ELECTROCHEMICAL DEGRADATION | Boron - chemistry | Electrochemical Techniques | Phenylethyl Alcohol - analogs & derivatives | Iron - chemistry | Sulfides - chemistry | Water Pollutants, Chemical - chemistry | Diamond - chemistry | Carbon - chemistry | Electrodes | Hydrogen Peroxide - chemistry | Hydroxyl Radical - chemistry | Catalysis | Kinetics | Hydrogen-Ion Concentration | Phenylethyl Alcohol - chemistry | Sulfur compounds | Hydroxides | Oxalic acid | Quinone | Resveratrol | Oxalates | Organic acids | Degradation | Catalysts | Anodizing | Mineralization | Iron | Anodes | Cathodes
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text 3,5-Dimethylisoxazoles Act As Acetyl-lysine-mimetic Bromodomain Ligands
by Hewings, David S and Wang, Minghua and Philpott, Martin and Fedorov, Oleg and Uttarkar, Sagar and Filippakopoulos, Panagis and Picaud, Sarah and Vuppusetty, Chaitanya and Marsden, Brian and Knapp, Stefan and Conway, Stuart J and Heightman, Tom D
Journal of Medicinal Chemistry, ISSN 0022-2623, 10/2011, Volume 54, Issue 19, pp. 6761 - 6770
Histone–lysine acetylation is a vital chromatin post-translational modification involved in the epigenetic regulation of gene transcription. Bromodomains bind... 
CHEMISTRY, MEDICINAL | PROTEIN | STRUCTURAL BASIS | INTERACTS | CGRP RECEPTOR ANTAGONISTS | HISTONE ACETYLATION | FAMILY | Phenylethyl Alcohol - analogs & derivatives | Stereoisomerism | Humans | Crystallography, X-Ray | Structure-Activity Relationship | Isoxazoles - chemical synthesis | CREB-Binding Protein - metabolism | Molecular Mimicry | Cytotoxins - pharmacology | Lysine - metabolism | Molecular Structure | Protein-Serine-Threonine Kinases - metabolism | Protein Structure, Tertiary | Cytotoxins - chemical synthesis | Models, Molecular | Nuclear Proteins - metabolism | Isoxazoles - chemistry | Isoxazoles - pharmacology | Transcription Factors - metabolism | Phenylethyl Alcohol - pharmacology | Cytotoxins - chemistry | Phenylethyl Alcohol - chemical synthesis | Protein Binding | Ligands | HeLa Cells | Histones - metabolism | Phenylethyl Alcohol - chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Hydroxytyrosol-Derived Compounds: A Basis for the Creation of New Pharmacological Agents for Cancer Prevention and Therapy
by Bernini, Roberta and Gilardini Montani, Maria Saveria and Merendino, Nicolò and Romani, Annalisa and Velotti, Francesca
Journal of Medicinal Chemistry, ISSN 0022-2623, 12/2015, Volume 58, Issue 23, pp. 9089 - 9107
Hydroxytyrosol [2-(3,4-dihydroxyphenyl)­ethanol, HTyr] is a phenolic compound found in olive leaves and fruits and extra-virgin olive oil, which has well-known... 
ANTIOXIDANT ACTIVITY | CONVENIENT SYNTHESIS | OXIDATIVE STRESS | CHEMISTRY, MEDICINAL | HYDROLYZABLE PHENOLIC-COMPOUNDS | LOW-DOSE ASPIRIN | PLATELET | VIRGIN OLIVE OIL | ACETATE | DERIVATIVES | CHEMOSELECTIVE ESTERIFICATION | Anticarcinogenic Agents - chemical synthesis | Antioxidants - chemistry | Apoptosis - drug effects | Phenylethyl Alcohol - analogs & derivatives | Antineoplastic Agents - chemical synthesis | Humans | Neoplasms - prevention & control | Antineoplastic Agents - pharmacology | Anticarcinogenic Agents - pharmacology | Anti-Inflammatory Agents - pharmacology | Antioxidants - chemical synthesis | Antioxidants - pharmacology | Antineoplastic Agents - chemistry | Drug Discovery | Neoplasms - drug therapy | Phenylethyl Alcohol - pharmacology | Animals | Anti-Inflammatory Agents - chemistry | Anticarcinogenic Agents - chemistry | Olive Oil - chemistry | Phenylethyl Alcohol - chemical synthesis | Anti-Inflammatory Agents - chemical synthesis | Cell Proliferation - drug effects | Neoplasms - pathology | Phenylethyl Alcohol - chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text In vitro assessment of antioxidant activity of tyrosol, resveratrol and their acetylated derivatives
by Vlachogianni, Ioanna C and Fragopoulou, Elizabeth and Kostakis, Ioannis K and Antonopoulou, Smaragdi
Food Chemistry, ISSN 0308-8146, 06/2015, Volume 177, pp. 165 - 173
Consumption of phenolic compounds is associated with beneficial effects in humans even though many of them are poorly absorbed. The aim of this study was to... 
Synthesis | Acetylation | Antioxidant | Tyrosol | Lipophilicity | Resveratrol | OXIDATION | LIPID-PEROXIDATION | MEDITERRANEAN DIET | PHENOLIC-COMPOUNDS | FOOD SCIENCE & TECHNOLOGY | INHIBITORY-ACTIVITY | VIRGIN OLIVE OIL | FLAVONOIDS | LIPOXYGENASE | POLYPHENOLS | NUTRITION & DIETETICS | BIOLOGICAL-ACTIVITY | CHEMISTRY, APPLIED | Free Radical Scavengers - pharmacology | Antioxidants - chemistry | Free Radical Scavengers - chemistry | Phenylethyl Alcohol - analogs & derivatives | Humans | Stilbenes - analysis | Stilbenes - chemistry | Stilbenes - pharmacology | Picrates - pharmacology | Biphenyl Compounds - pharmacology | Lipoxygenase Inhibitors - chemistry | Picrates - chemistry | Soybeans - enzymology | Lipid Peroxidation - drug effects | Serum | Biphenyl Compounds - chemistry | Phenylethyl Alcohol - analysis | Oxidation-Reduction | Linoleic Acid - chemistry | Antioxidants - pharmacology | Phenylethyl Alcohol - pharmacology | In Vitro Techniques | Lipoxygenase Inhibitors - pharmacology | Phenylethyl Alcohol - chemistry | Antioxidants | Analysis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Hydroxytyrosol and Its Potential Therapeutic Effects
by Hu, Ting and He, Xiao-Wei and Jiang, Jian-Guo and Xu, Xi-Lin
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 02/2014, Volume 62, Issue 7, pp. 1449 - 1455
As olive oil is the main source of calories in the Mediterranean diet, a large number of studies have been carried out to characterize its role in various... 
olive oil | biological activities | hydroxytyrosol | Mediterranean diet | PURIFIED HYDROXYTYROSOL | NATURAL ANTIOXIDANT | ANTIOXIDANT POLYPHENOLS | PLATELET-AGGREGATION | FOOD SCIENCE & TECHNOLOGY | BIOLOGICAL-ACTIVITIES | PULP EXTRACT | OLIVE OIL PHENOLS | IN-VITRO | MILL WASTE-WATER | AGRICULTURE, MULTIDISCIPLINARY | RICH | CHEMISTRY, APPLIED | Plant Extracts - chemistry | Phenylethyl Alcohol - analogs & derivatives | Plant Extracts - pharmacology | Humans | Drug Therapy | Olive Oil | Phenylethyl Alcohol - therapeutic use | Plant Oils - chemistry | Phenylethyl Alcohol - chemistry | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Interfacial Concentrations of Hydroxytyrosol and Its Lipophilic Esters in Intact Olive Oil-in-Water Emulsions: Effects of Antioxidant Hydrophobicity, Surfactant Concentration, and the Oil-to-Water Ratio on the Oxidative Stability of the Emulsions
by Almeida, João and Losada-Barreiro, Sonia and Costa, Marlene and Paiva-Martins, Fátima and Bravo-Díaz, Carlos and Romsted, Laurence S
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 06/2016, Volume 64, Issue 25, pp. 5274 - 5283
We determined the interfacial molarities of the antioxidants, AOs, hydroxytyrosol (HT), and HT fatty acid esters with chain lengths of 1 to 16 carbons in... 
antioxidant efficiency | fatty acid esters | hydroxytyrosol | VITAMIN-C | MECHANISM | FOOD SCIENCE & TECHNOLOGY | ALPHA-TOCOPHEROL | ALKYL ESTERS | DISTRIBUTIONS | MODEL FOOD EMULSION | GALLIC ACID | TEMPERATURE | AGRICULTURE, MULTIDISCIPLINARY | CHEMICAL-REACTIVITY | CHEMISTRY, APPLIED | DERIVATIVES | Antioxidants - chemistry | Oxidation-Reduction | Emulsions - chemistry | Esters - chemistry | Phenylethyl Alcohol - analogs & derivatives | Olive Oil - chemistry | Water - chemistry | Hydrophobic and Hydrophilic Interactions | Surface-Active Agents - chemistry | Phenylethyl Alcohol - chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Antioxidant ability of tyrosol and derivative-compounds in the presence of O 2 ( 1 Δ g )-species. Studies of synergistic antioxidant effect with commercial antioxidants
by Casadey, Rocío and Challier, Cecilia and Senz, Alejandro and Criado, Susana
Food Chemistry, ISSN 0308-8146, 07/2019, Volume 285, pp. 275 - 281
The exposure of fatty products to environmental light can trigger lipid oxidation in food through a sensitized-photooxidation process, which involves the... 
4-hydroxyphenethyl alcohol (PubChem CID: 10393) | L-Ascorbic acid (PubChem CID: 54670067) | Photodegradation | 3-hydroxyphenethyl alcohol (PubChem CID: 83404) | Singlet oxygen | Rose Bengal (PubChem CID: 69438) | (±)-6-Hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid (Trolox) (PubChem CID: 40634) | L-Triptophan (PubChem CID: 6305) | Methyl linoleate (PubChem CID: 5284421) | Phenolic antioxidants | 2-hydroxyphenethyl alcohol (PubChem CID: 82200) | Furfuryl alcohol (PubChem CID: 7361) | Antioxidants - chemistry | Oxidation-Reduction | Phenylethyl Alcohol - analogs & derivatives | Tryptophan - chemistry | Food Preservatives - pharmacology | Antioxidants - pharmacology | Isomerism | Drug Synergism | Phenylethyl Alcohol - pharmacology | Ultraviolet Rays | Food Preservatives - chemistry | Singlet Oxygen | Hydrogen-Ion Concentration | Linoleic Acids - chemistry | Phenylethyl Alcohol - chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Instability of, and generation of hydrogen peroxide by, phenolic compounds in cell culture media
by Long, Lee Hua and Hoi, Aina and Halliwell, Barry
Archives of Biochemistry and Biophysics, ISSN 0003-9861, 2010, Volume 501, Issue 1, pp. 162 - 169
Many papers in the literature have described complex effects of flavonoids and other polyphenols on cells in culture. In this paper we show that... 
Cell culture | DMEM | Hydrogen peroxide | Hesperetin | Naringenin | Apigenin | Resveratrol | Curcumin | Tyrosol | OXIDATION | APOPTOSIS | VIVO | BIOCHEMISTRY & MOLECULAR BIOLOGY | TEA | IN-VITRO | POLYPHENOLS | BIOPHYSICS | ANTIOXIDANT | PROSTATE-CANCER | Flavonoids - analysis | Oxidation-Reduction | Phenylethyl Alcohol - analogs & derivatives | Drug Stability | Depsides - analysis | Depsides - chemistry | Anthocyanins - chemistry | Phenols - analysis | Hydrogen Peroxide - analysis | Polyphenols | Cinnamates - analysis | Phenols - chemistry | Cell Culture Techniques | Cinnamates - chemistry | Phenylethyl Alcohol - analysis | Culture Media - chemistry | Flavonoids - chemistry | Anthocyanins - analysis | Phenylethyl Alcohol - chemistry | Cell research | Flavonoids | Flavones | Bioflavonoids
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Occurrence of Glycosidically Conjugated 1‑Phenylethanol and Its Hydrolase β‑Primeverosidase in Tea (Camellia sinensis) Flowers
by Zhou, Ying and Dong, Fang and Kunimasa, Aiko and Zhang, Yuqian and Cheng, Sihua and Lu, Jiamin and Zhang, Ling and Murata, Ariaki and Mayer, Frank and Fleischmann, Peter and Watanabe, Naoharu and Yang, Ziyin
Journal of Agricultural and Food Chemistry, ISSN 0021-8561, 08/2014, Volume 62, Issue 32, pp. 8042 - 8050
A previous study found that 1-phenylethanol (1PE) was a major endogenous volatile compound in tea (Camellia sinensis) flowers and can be transformed to... 
stereochemistry | primeveroside | 1-phenylethanol | primeverosidase | glucopyranoside | tea flower | DISACCHARIDE GLYCOSIDES | CATHARANTHUS-ROSEUS | FOOD SCIENCE & TECHNOLOGY | LEAVES | OOLONG TEA | TRITERPENE OLIGOGLYCOSIDES | GREEN TEA | MANUFACTURING PROCESS | AGRICULTURE, MULTIDISCIPLINARY | KEY ENZYME | CHEMISTRY, APPLIED | L-PHENYLALANINE | BOUND AROMA PRECURSORS | Camellia sinensis - chemistry | Gas Chromatography-Mass Spectrometry | Glycoside Hydrolases - genetics | Crops, Agricultural - growth & development | Substrate Specificity | Camellia sinensis - growth & development | Chromatography, High Pressure Liquid | Flowers - chemistry | Food Additives - chemistry | Odorants | Food Additives - analysis | Spectrometry, Mass, Electrospray Ionization | China | Gene Expression Regulation, Plant | Glycosides - isolation & purification | Nuclear Magnetic Resonance, Biomolecular | Crops, Agricultural - chemistry | Molecular Structure | Plant Proteins - metabolism | Phenylethyl Alcohol - analysis | Glycosides - chemistry | Recombinant Proteins - metabolism | Benzyl Alcohols - chemistry | Benzyl Alcohols - isolation & purification | Food Additives - isolation & purification | Glycosides - analysis | Crops, Agricultural - enzymology | Flowers - enzymology | Phenylethyl Alcohol - isolation & purification | Phenylethyl Alcohol - metabolism | Camellia sinensis - enzymology | Flowers - growth & development | Hydrolysis | Plant Proteins - genetics | Benzyl Alcohols - analysis | Glycosides - metabolism | Benzyl Alcohols - metabolism | Food Additives - metabolism | Glycoside Hydrolases - metabolism | Phenylethyl Alcohol - chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Hydroxytyrosol: from laboratory investigations to future clinical trials
by Granados‐Principal, Sergio and Quiles, José L and Ramirez‐Tortosa, Cesar L and Sanchez‐Rovira, Pedro and Ramirez‐Tortosa, M Carmen
Nutrition Reviews, ISSN 0029-6643, 04/2010, Volume 68, Issue 4, pp. 191 - 206
Mediterranean countries have lower rates of mortality from cardiovascular disease and cancer than Northern European or other Western countries. This has been... 
cardiovascular disease | olive oil | cancer | hydroxytyrosol | Mediterranean diet | Hydroxytyrosol | Cardiovascular disease | Olive oil | Cancer | SUNFLOWER OIL | OXIDATIVE STRESS | PHENOLIC-COMPOUNDS | LOW-DENSITY-LIPOPROTEIN | VIRGIN OLIVE OIL | FATTY-ACIDS | LONG-TERM ADAPTATION | MINOR COMPONENTS | NUTRITION & DIETETICS | DIETARY OILS | PERIPHERAL VASCULAR-DISEASE | Anti-Infective Agents - toxicity | Phenylethyl Alcohol - administration & dosage | Antioxidants - chemistry | Diet, Mediterranean | Phenylethyl Alcohol - analogs & derivatives | Cardiovascular Diseases - prevention & control | Humans | Neoplasms - prevention & control | Olive Oil | Platelet Aggregation Inhibitors - toxicity | Antioxidants - toxicity | Anti-Infective Agents - administration & dosage | Anti-Infective Agents - chemistry | Platelet Aggregation Inhibitors - administration & dosage | Antioxidants - administration & dosage | Platelet Aggregation Inhibitors - chemistry | Cardiovascular Diseases - mortality | Plant Oils - administration & dosage | Plant Oils - chemistry | Phenylethyl Alcohol - toxicity | Phenylethyl Alcohol - chemistry | Composition | Phytochemicals | Health aspects
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text Identification of p-hydroxybenzyl alcohol, tyrosol, phloretin and its derivate phloridzin as tyrosinase substrates
by Ortiz-Ruiz, Carmen Vanessa and Berna, Jose and Garcia-Molina, Maria del Mar and Tudela, Jose and Tomas, Virginia and Garcia-Canovas, Francisco
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 07/2015, Volume 23, Issue 13, pp. 3738 - 3746
In recent years, the hydroxyalkylphenols -hydroxybenzyl alcohol and tyrosol, and the compound phloretin and its derivate phloridzin have been described as... 
p-Hydroxybenzyl alcohol | Alternative substrate | Phloretin | Tyrosinase | Tyrosol | Phloridzin | P-Hydroxybenzyl alcohol | DIPHENOLASE ACTIVITY | CHEMISTRY, MEDICINAL | ANTITYROSINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | ACTION MECHANISM | 3,4-DIHYDROXYMANDELIC ACID | INDUCED MELANOGENESIS | MUSHROOM TYROSINASE | PATHWAY | MONOPHENOLS | STEADY-STATE | HYDROQUINONE | Fungal Proteins - chemistry | Benzyl Alcohols - chemistry | Phenylethyl Alcohol - analogs & derivatives | Substrate Specificity | Phlorhizin - chemistry | Enzyme Assays | Fungal Proteins - antagonists & inhibitors | Monophenol Monooxygenase - antagonists & inhibitors | Phenylacetates - chemistry | Levodopa - chemistry | Enzyme Inhibitors - chemistry | Phloretin - chemistry | Kinetics | Monophenol Monooxygenase - chemistry | Tyrosine - chemistry | Phenylethyl Alcohol - chemistry | Tyrosine | Physiological aspects | Quinone | Resveratrol
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text Solvent-controlled synthesis of tetranuclear cage-like copper(ii) silsesquioxanes. Remarkable features of the cage structures and their high catalytic activity in oxidation with peroxides
by Dronova, Marina S and Bilyachenko, Alexey N and Yalymov, Alexey I and Kozlov, Yuriy N and Shul'Pina, Lidia S and Korlyukov, Alexander A and Arkhipov, Dmitry E and Levitsky, Mikhail M and Shubina, Elena S and Shul'Pin, Georgiy B
Dalton Transactions, ISSN 1477-9226, 01/2014, Volume 43, Issue 2, pp. 872 - 882
Two principally different in their molecular architecture isomeric tetranuclear copper(II) silsesquioxanes, "Globule"-like compound... 
BUTYL HYDROPEROXIDE | SELECTIVE OXIDATION | ALKANE HYDROPEROXIDATION | COMPLEXES | CYCLOHEXANE | O-2-H2O2-VANADIUM DERIVATIVE-PYRAZINE-2-CARBOXYLIC ACID | HYDROGEN-PEROXIDE | COORDINATION POLYMERS | PRIMARY ALCOHOLS | CHEMISTRY, INORGANIC & NUCLEAR | Chemistry Techniques, Synthetic | Oxidation-Reduction | Solvents - chemistry | Molecular Conformation | Models, Molecular | Isomerism | tert-Butylhydroperoxide - chemistry | Hydrogen Peroxide - chemistry | Copper - chemistry | Organometallic Compounds - chemical synthesis | Benzene - chemistry | Organometallic Compounds - chemistry | Catalysis | Phenylethyl Alcohol - chemistry
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text Synthesis and antioxidant of activity of alkyl nitroderivatives of hydroxytyrosol
by Gallardo, Elena and Palma-Valdés, Rocío and Sarriá, Beatriz and Gallardo, Irene and De La Cruz, José P and Bravo, Laura and Mateos, Raquel and Espartero, José L
Molecules, ISSN 1420-3049, 05/2016, Volume 21, Issue 5, p. 656
A series of alkyl nitrohydroxytyrosyl ether derivatives has been synthesized from free hydroxytyrosol (HT), the natural olive oil phenol, in order to increase... 
Hydroxytyrosol | Parkinson's disease | Nitrocatechol | Antioxidant activity | Alkyl nitrohydroxytyrosyl derivatives | alkyl nitrohydroxytyrosyl derivatives | ETHERS | PHENOLIC-COMPOUNDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | TYROSYL | PREVENTION | hydroxytyrosol | nitrocatechol | antioxidant activity | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | Antioxidants - chemistry | Fluorescence Recovery After Photobleaching | Oxidation-Reduction | Free Radical Scavengers - chemistry | Nitrogen Dioxide - therapeutic use | Phenylethyl Alcohol - analogs & derivatives | Humans | Antioxidants - chemical synthesis | Carbon - chemistry | Sulfonic Acids - chemistry | Antioxidants - therapeutic use | Reactive Oxygen Species - chemistry | Nitrogen Dioxide - chemistry | Oxygen - chemistry | Phenol - chemistry | Sulfonic Acids - therapeutic use | Benzothiazoles - chemistry | Phenylethyl Alcohol - chemical synthesis | Sesame Oil - chemistry | Phenols - chemistry | Benzothiazoles - therapeutic use | Free Radical Scavengers - therapeutic use | Phenylethyl Alcohol - therapeutic use | Phenylethyl Alcohol - chemistry | Parkinson’s disease
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
14. Full Text Combined Ruthenium(II) and Lipase Catalysis for Efficient Dynamic Kinetic Resolution of Secondary Alcohols. Insight into the Racemization Mechanism
by Martín-Matute, Belén and Edin, Michaela and Bogár, Krisztián and Kaynak, F. Betül and Bäckvall, Jan-E and Stockholms universitet and Naturvetenskapliga fakulteten and Institutionen för organisk kemi
Journal of the American Chemical Society, ISSN 0002-7863, 06/2005, Volume 127, Issue 24, pp. 8817 - 8825
Pentaphenylcyclopentadienyl ruthenium complexes (3) are excellent catalysts for the racemization of secondary alcohols at ambient temperature. The combination... 
KETONES | ROUTE | ASYMMETRIC TRANSFER HYDROGENATION | ENZYMATIC RESOLUTION | METAL-CATALYSTS | COMPLEXES | AMBIENT-TEMPERATURE | AMINO ALCOHOLS | HYDROXY ACID-DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | HYDRIDE | Alcohols - chemistry | Organometallic Compounds - chemical synthesis | Stereoisomerism | Crystallography, X-Ray | Organometallic Compounds - chemistry | Molecular Structure | Catalysis | Kinetics | Lipase - chemistry | Ruthenium - chemistry | Phenylethyl Alcohol - chemistry | Ruthenium | Research | Chemical properties | Catalysts | Alcohols
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
15. Full Text Oxidative DNA damage is prevented by extracts of olive oil, hydroxytyrosol, and other olive phenolic compounds in human blood mononuclear cells and HL60 cells
by Fabiani, Roberto and Rosignoli, Patrizia and De Bartolomeo, Angelo and Fuccelli, Raffaela and Servili, Maurizio and Montedoro, Gian Francesco and Morozzi, Guido
Journal of Nutrition, ISSN 0022-3166, 08/2008, Volume 138, Issue 8, pp. 1411 - 1416
Our aim in this study was to provide further support to the hypothesis that phenolic compounds may play an important role in the anticarcinogenic properties of... 
DNA Damage - drug effects | Leukocytes, Mononuclear - metabolism | Plant Oils - pharmacology | Leukocytes, Mononuclear - drug effects | Antioxidants - chemistry | Phenylethyl Alcohol - analogs & derivatives | Humans | Hydrogen Peroxide - pharmacology | Antioxidants - pharmacology | Olive Oil | Dose-Response Relationship, Drug | Phenylethyl Alcohol - pharmacology | HL-60 Cells | Phenols - chemistry | Oxidative Stress - drug effects | Plant Oils - chemistry | Olea - chemistry | Phenols - pharmacology | Phenylethyl Alcohol - chemistry | Prevention | Usage | DNA damage | Phenols | Olive oil | Health aspects | Cancer
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights