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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
Applied Microbiology and Biotechnology, ISSN 0175-7598, 5/2019, Volume 103, Issue 9, pp. 3761 - 3771
Sulfation is an important way for detoxifying xenobiotics and endobiotics including catechols. Enzymatic sulfation occurs usually with high chemo- and/or... 
Life Sciences | Biotechnology | p -Nitrophenyl sulfate | Directed evolution | Microbiology | Microbial Genetics and Genomics | Sulfotransferase | Catechols | 4-Aminoantipyrine | CELLS | METABOLITES | ASSAY | PHENOL | SCREENING SYSTEMS | INHIBITION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENZYMES | p-Nitrophenyl sulfate | Sulfates - metabolism | Magnetic Resonance Spectroscopy | Bacterial Proteins - chemistry | Bacterial Proteins - genetics | Arylsulfotransferase - chemistry | Substrate Specificity | Catechols - chemistry | Ampyrone - chemistry | Directed Molecular Evolution | Arylsulfotransferase - genetics | Desulfitobacterium - enzymology | Sulfates - chemistry | Bacterial Proteins - metabolism | Desulfitobacterium - chemistry | Desulfitobacterium - genetics | Kinetics | Ampyrone - metabolism | Arylsulfotransferase - metabolism | Catechols - metabolism | Tyrosine sulfation | Physiological aspects | Catechin | Observations | Transferases | Natural history | Stoichiometry | Nuclear magnetic resonance--NMR | Nitrophenol | Colorimetry | Sulfates | Coefficient of variation | Optimization | Magnetic resonance spectroscopy | Aromatic compounds | Efficiency | Evolution | Catalysis | Laboratory apparatus | Xenobiotics | Aryl sulfotransferase | Regioselectivity | p-Nitrophenol | Mass spectroscopy | Liquid chromatography | High-performance liquid chromatography | Sulfation | Screening | Sulfate | Mass spectrometry
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 2008, Volume 380, Issue 4, pp. 667 - 680
Journal Article
Analytical and Bioanalytical Chemistry, ISSN 1618-2642, 2/2013, Volume 405, Issue 4, pp. 1425 - 1429
Journal Article
Journal Article
Human Reproduction, ISSN 0268-1161, 07/2017, Volume 32, Issue 7, pp. 1465 - 1473
Abstract STUDY QUESTION Are bisphenol A (BPA) and BPA analogs (BPA-A) safe for male human reproductive function? SUMMARY ANSWER The endocrine function of human... 
anti-androgenic compounds | bisphenols | insulin-like factor 3 | testosterone | Leydig cells | endocrine disruptor | human testis | inhibin B | Sertoli cells | reproductive function | SPERM DNA-DAMAGE | UNITED-STATES | SERUM TESTOSTERONE CONCENTRATION | MASS-SPECTROMETRY METHOD | DIGLYCIDYL ETHER BADGE | SEMEN QUALITY | OBSTETRICS & GYNECOLOGY | REPRODUCTIVE BIOLOGY | HUMAN EXPOSURE | HORMONE CONCENTRATIONS | WIDESPREAD OCCURRENCE | HUMAN URINE | Gene Expression Regulation, Enzymologic - drug effects | Leydig Cells - cytology | Testis - metabolism | Apoptosis - drug effects | Benzhydryl Compounds - toxicity | Phenols - toxicity | Humans | Glucuronidase - metabolism | Male | Leydig Cells - drug effects | Testis - secretion | Nonsteroidal Anti-Androgens - chemistry | Benzhydryl Compounds - chemistry | Sertoli Cells - drug effects | Testis - drug effects | Glucuronosyltransferase - genetics | Testosterone - metabolism | Leydig Cells - metabolism | Sertoli Cells - cytology | Adult | Steryl-Sulfatase - metabolism | Sertoli Cells - metabolism | Steryl-Sulfatase - genetics | Nonsteroidal Anti-Androgens - toxicity | Reproducibility of Results | Sertoli Cells - secretion | Testosterone - secretion | Insulin - agonists | Sulfones - toxicity | Testis - cytology | Endocrine Disruptors - chemistry | Tissue Culture Techniques | Arylsulfotransferase - genetics | Epoxy Compounds - toxicity | Endocrine Disruptors - toxicity | Leydig Cells - secretion | Insulin - metabolism | Proteins - agonists | Proteins - metabolism | Glucuronidase - genetics | Glucuronosyltransferase - metabolism | Testosterone - antagonists & inhibitors | Phenols - chemistry | Arylsulfotransferase - metabolism | Proteins - antagonists & inhibitors | Index Medicus | Life Sciences | Santé publique et épidémiologie
Journal Article