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Drug Metabolism and Disposition, ISSN 0090-9556, 06/2018, Volume 46, Issue 6, pp. 860 - 864
Journal Article
Molecular Biology Reports, ISSN 0301-4851, 12/2018, Volume 45, Issue 6, pp. 2571 - 2584
N-ethyl-N-nitrosourea (ENU) is highly used in rodent models of tumerogenesis/carcinogenesis. Xenografting human-cancer tissues/cells with estradiol (E2)... 
Estrogen sulfotransferase | Oxidative stress | Hepatocellular toxicity | N-ethyl-N-nitrosourea (ENU) | Xenograft-estradiol | SPRAGUE-DAWLEY RATS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLUTATHIONE-PEROXIDASE | INDUCED MAMMARY-TUMORS | SPECIAL EMPHASIS | GAMMA-GLUTAMYL-TRANSPEPTIDASE | REDOX REGULATION | GENE-EXPRESSION | PRENEOPLASTIC LESIONS | SUPEROXIDE-DISMUTASE | Estradiol - blood | Catalase - drug effects | Rats, Wistar | Antioxidants - metabolism | Humans | Oxidants - metabolism | Superoxide Dismutase-1 - drug effects | Breast Neoplasms - metabolism | Sulfotransferases - drug effects | Heterografts | Female | Estradiol - pharmacology | DNA Damage - drug effects | Sulfotransferases - genetics | Estradiol - metabolism | Oxidation-Reduction | Liver - metabolism | Rats | Xenograft Model Antitumor Assays - methods | Breast Neoplasms - drug therapy | Ethylnitrosourea - pharmacology | Catalase - metabolism | Ethylnitrosourea - metabolism | Animals | Oxidative Stress - drug effects | Antioxidants | Phosphatases | Arsenic | Phenols | Genetic research | Breast cancer | Glutamate | Estradiol | Alkaline phosphatase | Animal models | Toxicity | DNA damage | Liver | Acetylcysteine | Estrone sulfotransferase | Pyruvic acid | Superoxide dismutase | Carcinogenesis | Catalase | Rodents | Xenografts | Peroxidase | Bioinformatics | Enzyme-linked immunosorbent assay | Free radicals | Gynecology | Data processing | Exploration | Ethyl nitrosourea | Peritoneum | Index Medicus
Journal Article
Environmental Toxicology and Pharmacology, ISSN 1382-6689, 03/2018, Volume 58, pp. 196 - 201
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, pp. e73587 - e73587
Drug metabolizing enzymes play a key role in the metabolism, elimination and detoxification of xenobiotics, drugs and endogenous molecules. While their... 
HUMAN CATECHOLAMINE SULFOTRANSFERASE | SITE | CRYSTAL-STRUCTURE | ESTROGEN SULFOTRANSFERASE | DOCKING | MULTIDISCIPLINARY SCIENCES | DRUG DISCOVERY | SUBSTRATE-INHIBITION | STRUCTURAL GENOMICS | METABOLIZING-ENZYMES | PREDICTIVE MODELS | Protein Structure, Tertiary | Humans | Arylsulfotransferase - chemistry | Models, Molecular | Crystallography, X-Ray | Small Molecule Libraries - metabolism | Xenobiotics - chemistry | Molecular Dynamics Simulation | Small Molecule Libraries - chemistry | Thermodynamics | Computer Simulation | Protein Binding | Ligands | Sulfotransferases - metabolism | Molecular Structure | Xenobiotics - metabolism | Arylsulfotransferase - metabolism | Binding Sites | Quantitative Structure-Activity Relationship | Sulfotransferases - chemistry | Complications and side effects | Enzymes | Analysis | Molecular dynamics | Physiological aspects | Xenobiotics | Investigations | Drugs | Energy use | Toxicity | Estrone sulfotransferase | Thyroid gland | Hormones | Structure-activity relationships | Flexibility | Proteins | Metabolites | Docking | Atomic structure | Pollutants | Bioinformatics | Excretion | Automation | Dopamine | Computer simulation | Detoxification | Bioavailability | Metabolism | Binders | Substrates | Side effects | Molecular modelling | Isoforms | Predictions | Binding sites | Index Medicus
Journal Article
Breast cancer research : BCR, ISSN 1465-5411, 06/2004, Volume 6, Issue 5, pp. R488 - 498
Journal Article
Journal of Steroid Biochemistry and Molecular Biology, ISSN 0960-0760, 09/2017, Volume 172, pp. 46 - 54
Celecoxib is known to alter the preferred position of SULT2A1-catalyzed sulfonation of 17β-estradiol (17β-E2) and other estrogens from the 3- to the... 
Sulfotransferases | Estrogen | Quercetin | Celecoxib | Triclosan | Steroids | Cancer | CONJUGATED EQUINE ESTROGENS | HUMAN-BREAST-CANCER | MCF-7 | BIOCHEMISTRY & MOLECULAR BIOLOGY | PREVENTION | HORMONAL BASIS | HUMAN CYTOSOLIC SULFOTRANSFERASES | INHIBITION | METABOLISM | ENDOCRINOLOGY & METABOLISM | POSTMENOPAUSAL WOMEN | MAMMARY EPITHELIAL-CELLS | Liver - enzymology | Species Specificity | Humans | Male | Isoenzymes - chemistry | Triclosan - pharmacology | Celecoxib - chemistry | Nitrophenols - chemistry | Hepatocytes - cytology | Liver - drug effects | Nitrophenols - pharmacology | Isoenzymes - metabolism | Sulfates - chemistry | Adult | Female | Sulfotransferases - metabolism | Estradiol - pharmacology | Hepatocytes - drug effects | Recombinant Proteins - metabolism | Sulfotransferases - genetics | Estradiol - metabolism | Estrone - pharmacology | Gene Expression | Quercetin - chemistry | Sulfates - metabolism | Isoenzymes - genetics | Arylsulfotransferase - chemistry | Models, Molecular | Rats | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Celecoxib - pharmacology | Arylsulfotransferase - genetics | Rats, Sprague-Dawley | Triclosan - chemistry | Animals | Quercetin - pharmacology | Estrone - metabolism | Liver - cytology | Molecular Docking Simulation | Structural Homology, Protein | Primary Cell Culture | Arylsulfotransferase - metabolism | Sulfotransferases - chemistry | Hepatocytes - enzymology | COX-2 inhibitors | Dehydroepiandrosterone | Liver | Phenols | Tryptophan | Angiogenesis inhibitors | Sulfates | Estradiol | Estrogens | Estrone sulfotransferase | 17β-Estradiol | p-Nitrophenol | Breast cancer | Glycine | Cytosol | Studies | Steroid sulfatase | Rodents | Sulfonation | Estrone | Sulfate | Steroid hormones | Index Medicus
Journal Article
Journal Article
Journal Article