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Journal of Enzyme Inhibition and Medicinal Chemistry, ISSN 1475-6366, 11/2016, Volume 31, Issue sup4, pp. 125 - 131
Phenolic bis Mannich bases having the chemical structure of 1-[3,5-bis-aminomethyl-4-hydroxyphenyl]-3-(4-halogenophenyl)-2-propen-1-ones (1a-c, 2a-c, 3a-c)... 
chalcone | phenol | Mannich bases | Carbonic anhydrase | cytotoxicity | CARBONIC-ANHYDRASE | CHEMISTRY, MEDICINAL | CANCER CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PIPERIDINOLS | INHIBITION | ANTICANCER | BIOLOGICAL EVALUATION | AGENTS | DERIVATIVES | Chalcones - chemistry | Mouth Neoplasms - drug therapy | Carbonic Anhydrase Inhibitors - chemistry | Antineoplastic Agents - chemical synthesis | Carcinoma, Squamous Cell - metabolism | Carcinoma, Squamous Cell - pathology | Humans | Carbonic Anhydrase II - metabolism | Mouth Neoplasms - metabolism | Structure-Activity Relationship | Carbonic Anhydrase I - metabolism | Carbonic Anhydrase II - antagonists & inhibitors | Mannich Bases - chemical synthesis | Dose-Response Relationship, Drug | Chalcones - chemical synthesis | Isoenzymes - metabolism | Chalcones - pharmacology | Mannich Bases - pharmacology | Antineoplastic Agents - pharmacology | Halogens - chemistry | Molecular Structure | Phenols - pharmacology | Cell Line | Solubility | Carbonic Anhydrase Inhibitors - chemical synthesis | Carbonic Anhydrase Inhibitors - pharmacology | Antineoplastic Agents - chemistry | Mannich Bases - chemistry | Carcinoma, Squamous Cell - drug therapy | Halogens - pharmacology | Carbonic Anhydrase I - antagonists & inhibitors | Mouth Neoplasms - pathology | Phenols - chemistry | Cell Proliferation - drug effects | Isoenzymes - antagonists & inhibitors | Drug Screening Assays, Antitumor
Journal Article
Journal of Food Science, ISSN 0022-1147, 09/2016, Volume 81, Issue 9, pp. C2218 - C2223
A simple and efficient method based on high‐performance thin‐layer chromatography coupled with 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) bioautography (HPTLC‐DPPH)... 
Coreopsis tinctoria | identification | HPTLC‐DPPH | antioxidant activity | herbal tea | Herbal tea | Identification | HPTLC-DPPH | Antioxidant activity | NUTT | CAFFEOYLQUINIC ACIDS | FOOD SCIENCE & TECHNOLOGY | COMPONENTS | FLAVONOIDS | MASS-SPECTROMETRY | LIQUID-CHROMATOGRAPHY | PRODUCTS | SEPARATION | EXTRACTS | GLUCOSE-TOLERANCE | Chlorogenic Acid - analysis | Plant Extracts - chemistry | Quinic Acid - analogs & derivatives | Chlorogenic Acid - pharmacology | Plant Extracts - pharmacology | Chromatography, Thin Layer - methods | Flavanones - pharmacology | Picrates - metabolism | Flavanones - analysis | Antioxidants - pharmacology | Biphenyl Compounds - metabolism | Chlorogenic Acid - analogs & derivatives | Chalcones - pharmacology | Coreopsis - chemistry | Chalcones - analysis | Quinic Acid - analysis | Quinic Acid - pharmacology | Teas, Herbal - analysis | Densitometry | Antioxidants - analysis | Chrysanthemum - chemistry | Quality Control | Antioxidants | Nutritional aspects | Tea (Plant) | Comparative analysis | High performance liquid chromatography | Methods | Herbs | Principal components analysis | Chromatography | Quality control | Cluster analysis | Scanning | Ethanol | Chlorogenic acid | Pharmacology | Clustering | Biological activity | Densitometers | Tea | Acids | Functional foods | Supermarkets | Biomarkers | Thin layer chromatography | Ethyl alcohol | Chemometrics
Journal Article
International Journal of Developmental Neuroscience, ISSN 0736-5748, 2011, Volume 29, Issue 7, pp. 701 - 710
• A novel effect of dietary compounds on neuroblastoma viability is presented. • A p53- and caspase-3 independent mechanism of cell death is demonstrated. •... 
Ayurveda | Pediatric cancer | Chemotherapy | Akt | Nutrition | OXIDATIVE STRESS | ACTIVATION | CURCUMIN | RATS | DEVELOPMENTAL BIOLOGY | CHEMOTHERAPY-INDUCED APOPTOSIS | NEUROSCIENCES | TRAUMATIC BRAIN-INJURY | FERULIC ACID | PATHWAY | COMBINATION KAN-JANG | NF-KAPPA-B | Plant Extracts - chemistry | Humans | bcl-X Protein - genetics | NF-kappa B - metabolism | Antineoplastic Agents - therapeutic use | Antineoplastic Agents - administration & dosage | Diterpenes, Abietane - administration & dosage | Curcumin - administration & dosage | Proto-Oncogene Proteins c-akt - genetics | Tumor Suppressor Protein p53 - genetics | Proto-Oncogene Proteins c-bcl-2 - metabolism | Caspases - metabolism | Neuroblastoma - diet therapy | Diterpenes - administration & dosage | Chalcones - pharmacology | Anti-Inflammatory Agents - administration & dosage | Antineoplastic Agents - pharmacology | Cell Death - drug effects | Chromones - pharmacology | Proto-Oncogene Proteins c-akt - metabolism | Neuroblastoma - pathology | Diterpenes - pharmacology | Cell Survival - drug effects | Anti-Inflammatory Agents - pharmacology | Coumarins - administration & dosage | Curcumin - pharmacology | Tumor Suppressor Protein p53 - metabolism | Morpholines - pharmacology | Coumarins - pharmacology | Diterpenes, Abietane - pharmacology | Diet | Chalcones - administration & dosage | Neuroblastoma - drug therapy | Cell Line, Tumor | bcl-X Protein - metabolism | Proto-Oncogene Proteins c-bcl-2 - genetics | Proto-Oncogene Proteins c-akt - antagonists & inhibitors | Medicine, Ayurvedic | Cell death | Biochemistry | Neuroblastoma | Tumor proteins | Cancer | nutrition | chemotherapy | pediatric cancer
Journal Article
Journal Article
Journal Article
Biological and Pharmaceutical Bulletin, ISSN 0918-6158, 2007, Volume 30, Issue 1, pp. 193 - 196
Journal Article
BioMetals, ISSN 0966-0844, 6/2016, Volume 29, Issue 3, pp. 515 - 526
Complexes [Au(PyCT4BrPh)Cl]Cl (1), [Pt(PyCT4BrPh)Cl]0.5KCl (2), and [Pd(PyCT4BrPh)Cl]KCl (3) were obtained with 3-(4-bromophenyl)-1-pyridin-2-ylprop-2-en-1-one... 
Biochemistry, general | Microbiology | Thiosemicarbazone | Topoisomerase IB | Plant Physiology | Medicine/Public Health, general | Thioredoxin reductase | Chalcone | Cell Biology | Life Sciences | Pharmacology/Toxicology | Metal complexes | Cytotoxic activities | TUMOR-CELL LINES | BIOCHEMISTRY & MOLECULAR BIOLOGY | COMPOUND | THIOREDOXIN REDUCTASE-ACTIVITY | INHIBITION | SEMICARBAZONES | PHARMACOLOGY | AGENTS | CHALCONE-DERIVED THIOSEMICARBAZONES | BIOACTIVITIES | Pyridines - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Structure-Activity Relationship | Enzyme Inhibitors - chemical synthesis | Dose-Response Relationship, Drug | Thiosemicarbazones - chemistry | Thioredoxin-Disulfide Reductase - metabolism | Enzyme Inhibitors - chemistry | Coordination Complexes - pharmacology | Antineoplastic Agents - pharmacology | Molecular Structure | Thiosemicarbazones - pharmacology | Cell Survival - drug effects | DNA Topoisomerases, Type I - metabolism | Enzyme Inhibitors - pharmacology | Pyridines - chemical synthesis | Thiosemicarbazones - chemical synthesis | Antineoplastic Agents - chemistry | Coordination Complexes - chemistry | Cell Line, Tumor | Coordination Complexes - chemical synthesis | Cell Proliferation - drug effects | Pyridines - pharmacology | Thioredoxin-Disulfide Reductase - antagonists & inhibitors | Drug Screening Assays, Antitumor | Enzymes | Leukemia | Investigations | Gold | Cytotoxicity | Biochemistry
Journal Article