Life Sciences, ISSN 0024-3205, 2005, Volume 76, Issue 16, pp. 1835 - 1847
The purine analogue, allopurinol, has been in clinical use for more than 30 years as an inhibitor of xanthine oxidase (XO) in the treatment of hyperuricemia...
Pyrimidine metabolism | Xanthine oxidase inhibitor | Febuxostat | Purine metabolism | MEDICINE, RESEARCH & EXPERIMENTAL | TEI-6720 | xanthine oxidase inhibitor | purine metabolism | NUCLEOSIDE-PHOSPHORYLASE | ALLOPURINOL HYPERSENSITIVITY SYNDROME | OROTIDYLATE DECARBOXYLASE | OXIDASE INHIBITOR | KINETIC-PROPERTIES | pyrimidine metabolism | THERAPY | RENAL-FAILURE | PHARMACOLOGY & PHARMACY | febuxostat | PHOSPHORIBOSYLTRANSFERASE | ENZYMATIC SYNTHESIS | Animals | Milk - enzymology | Xanthine Dehydrogenase - antagonists & inhibitors | Enzyme Inhibitors - chemistry | Enzyme Inhibitors - pharmacology | Thiazoles - chemistry | Molecular Structure | Thiazoles - pharmacology | Kinetics | Xanthine Oxidase - antagonists & inhibitors | Oxidases | Care and treatment | Biological products | Iron compounds | Metabolites | Molybdenum compounds | Heterocyclic compounds | Gout | Physiological aspects | Phosphorylase
Pyrimidine metabolism | Xanthine oxidase inhibitor | Febuxostat | Purine metabolism | MEDICINE, RESEARCH & EXPERIMENTAL | TEI-6720 | xanthine oxidase inhibitor | purine metabolism | NUCLEOSIDE-PHOSPHORYLASE | ALLOPURINOL HYPERSENSITIVITY SYNDROME | OROTIDYLATE DECARBOXYLASE | OXIDASE INHIBITOR | KINETIC-PROPERTIES | pyrimidine metabolism | THERAPY | RENAL-FAILURE | PHARMACOLOGY & PHARMACY | febuxostat | PHOSPHORIBOSYLTRANSFERASE | ENZYMATIC SYNTHESIS | Animals | Milk - enzymology | Xanthine Dehydrogenase - antagonists & inhibitors | Enzyme Inhibitors - chemistry | Enzyme Inhibitors - pharmacology | Thiazoles - chemistry | Molecular Structure | Thiazoles - pharmacology | Kinetics | Xanthine Oxidase - antagonists & inhibitors | Oxidases | Care and treatment | Biological products | Iron compounds | Metabolites | Molybdenum compounds | Heterocyclic compounds | Gout | Physiological aspects | Phosphorylase
Journal Article
Hypertension, ISSN 0194-911X, 05/2013, Volume 61, Issue 5, pp. 1091 - 1102
Elevation of circulating nitrite (NO2) levels causes vasodilatation and lowers blood pressure in healthy volunteers. Whether these effects and the underpinning...
red blood cells | nitric oxide | vascular biology | hypertension | CHRONIC HEART-FAILURE | ORAL NITRITE | RESISTANT HYPERTENSION | DIETARY NITRATE | BLOOD-PRESSURE | OXIDE SYNTHASE | L-ARGININE | PERIPHERAL VASCULAR DISEASE | ISCHEMIA-REPERFUSION | HUMAN CIRCULATION | INORGANIC NITRATE | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Middle Aged | Rats, Inbred WKY | Hypertension - drug therapy | Male | Dose-Response Relationship, Drug | Hypertension - blood | Nitrites - blood | Female | Blood Pressure - drug effects | Blood Pressure - physiology | Erythrocytes - enzymology | Vasodilation - physiology | Disease Models, Animal | Rats, Inbred SHR | Xanthine Dehydrogenase - drug effects | Translational Medical Research | Enzyme Inhibitors - pharmacology | Rats | Nitrites - pharmacology | Hypertension - physiopathology | Nitrites - therapeutic use | Cross-Over Studies | Animals | Xanthine Dehydrogenase - physiology | Allopurinol - pharmacology | Signal Transduction - physiology | Vasodilation - drug effects
red blood cells | nitric oxide | vascular biology | hypertension | CHRONIC HEART-FAILURE | ORAL NITRITE | RESISTANT HYPERTENSION | DIETARY NITRATE | BLOOD-PRESSURE | OXIDE SYNTHASE | L-ARGININE | PERIPHERAL VASCULAR DISEASE | ISCHEMIA-REPERFUSION | HUMAN CIRCULATION | INORGANIC NITRATE | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Middle Aged | Rats, Inbred WKY | Hypertension - drug therapy | Male | Dose-Response Relationship, Drug | Hypertension - blood | Nitrites - blood | Female | Blood Pressure - drug effects | Blood Pressure - physiology | Erythrocytes - enzymology | Vasodilation - physiology | Disease Models, Animal | Rats, Inbred SHR | Xanthine Dehydrogenase - drug effects | Translational Medical Research | Enzyme Inhibitors - pharmacology | Rats | Nitrites - pharmacology | Hypertension - physiopathology | Nitrites - therapeutic use | Cross-Over Studies | Animals | Xanthine Dehydrogenase - physiology | Allopurinol - pharmacology | Signal Transduction - physiology | Vasodilation - drug effects
Journal Article
Nature Communications, ISSN 2041-1723, 03/2015, Volume 6, Issue 1, p. 6555
Activation of the NLRP3 inflammasome by microbial ligands or tissue damage requires intracellular generation of reactive oxygen species (ROS). We present...
ALLOPURINOL | OXIDASE | IL-1-BETA PRODUCTION | CONVERSION | MULTIDISCIPLINARY SCIENCES | IDENTIFICATION | HYPERTENSION | INHIBITOR | URIC-ACID | DEHYDROGENASE | NALP3 INFLAMMASOME | Phosphorylation | Calcium - metabolism | NLR Family, Pyrin Domain-Containing 3 Protein | Xanthine Dehydrogenase - antagonists & inhibitors | Xanthine Dehydrogenase - genetics | Caspase 1 - immunology | Carrier Proteins - drug effects | Autophagy | Gene Knockdown Techniques | Macrophages - secretion | Xanthine Dehydrogenase - immunology | Reactive Oxygen Species - immunology | Proto-Oncogene Proteins c-akt - metabolism | Real-Time Polymerase Chain Reaction | Calcium Phosphates - pharmacology | Carrier Proteins - immunology | Macrophages - immunology | Interleukin-1beta - secretion | Signal Transduction | Mice, Inbred C57BL | Peritonitis - immunology | Xanthine Oxidase - immunology | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Uric Acid - immunology | Monocytes | Animals | Lipopolysaccharides - pharmacology | Mice | In Vitro Techniques
ALLOPURINOL | OXIDASE | IL-1-BETA PRODUCTION | CONVERSION | MULTIDISCIPLINARY SCIENCES | IDENTIFICATION | HYPERTENSION | INHIBITOR | URIC-ACID | DEHYDROGENASE | NALP3 INFLAMMASOME | Phosphorylation | Calcium - metabolism | NLR Family, Pyrin Domain-Containing 3 Protein | Xanthine Dehydrogenase - antagonists & inhibitors | Xanthine Dehydrogenase - genetics | Caspase 1 - immunology | Carrier Proteins - drug effects | Autophagy | Gene Knockdown Techniques | Macrophages - secretion | Xanthine Dehydrogenase - immunology | Reactive Oxygen Species - immunology | Proto-Oncogene Proteins c-akt - metabolism | Real-Time Polymerase Chain Reaction | Calcium Phosphates - pharmacology | Carrier Proteins - immunology | Macrophages - immunology | Interleukin-1beta - secretion | Signal Transduction | Mice, Inbred C57BL | Peritonitis - immunology | Xanthine Oxidase - immunology | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Uric Acid - immunology | Monocytes | Animals | Lipopolysaccharides - pharmacology | Mice | In Vitro Techniques
Journal Article
Advances in experimental medicine and biology, ISSN 0065-2598, 2019, Volume 1127, p. 59
Inhibition of xanthine oxidoreductase (XOR) has proven beneficial in a plethora of inflammatory disease processes due to a net reduction in pro-inflammatory...
Nitrates - chemistry | Oxidants - chemistry | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Inflammation | Fatty Acids - pharmacology
Nitrates - chemistry | Oxidants - chemistry | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Inflammation | Fatty Acids - pharmacology
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2015, Volume 10, Issue 5, p. e0124150
Ectopic calcification is a driving force for a variety of diseases, including kidney stones and atherosclerosis, but initiating factors remain largely unknown....
MALPIGHIAN TUBULES | NANOBACTERIA | XANTHINE OXIDOREDUCTASE | MEDICAL-MANAGEMENT | MULTIDISCIPLINARY SCIENCES | CALCIUM | GROWTH | RISK | CALCIFICATION | PLAQUE | INSIGHTS | Xanthine Dehydrogenase - metabolism | RNA, Small Interfering - genetics | Cation Transport Proteins - antagonists & inhibitors | Kidney - pathology | Xanthine Dehydrogenase - antagonists & inhibitors | Zinc - metabolism | Humans | Xanthine Dehydrogenase - genetics | Drosophila Proteins - metabolism | Drosophila melanogaster - genetics | Malpighian Tubules - chemistry | Drosophila melanogaster - metabolism | Kidney - metabolism | Cation Transport Proteins - metabolism | Dietary Proteins - pharmacology | Cation Transport Proteins - genetics | Malpighian Tubules - drug effects | Drosophila Proteins - antagonists & inhibitors | Disease Models, Animal | X-Ray Absorption Spectroscopy | Gene Expression | Kidney - drug effects | Chelating Agents - pharmacology | Kidney Calculi - metabolism | Kidney Calculi - pathology | Ethylenediamines - pharmacology | Animals | Dogs | Allopurinol - pharmacology | Drosophila Proteins - genetics | Malpighian Tubules - pathology | Kidney Calculi - genetics | Kidney Calculi - prevention & control | RNA, Small Interfering - metabolism | Care and treatment | Drosophila | Fossilization | Diagnosis | Research | Risk factors | Zinc | Kidney stones | Calcification (ectopic) | Dehydrogenases | Disease | Xanthine dehydrogenase | Biology | Hydroxyapatite | Stone | Urology | Etiology | Mineralization | Rodents | Atherosclerosis | Aging | Physiology | Inhibition | Plaques | Spectroscopy | Kidneys | Pharmacology | Xanthine | Metabolism | Zinc transporter | Diet | Insects | Arteriosclerosis | Calcification | Lithiasis | Trace elements | Mutation | Transporter | Kidney transplantation
MALPIGHIAN TUBULES | NANOBACTERIA | XANTHINE OXIDOREDUCTASE | MEDICAL-MANAGEMENT | MULTIDISCIPLINARY SCIENCES | CALCIUM | GROWTH | RISK | CALCIFICATION | PLAQUE | INSIGHTS | Xanthine Dehydrogenase - metabolism | RNA, Small Interfering - genetics | Cation Transport Proteins - antagonists & inhibitors | Kidney - pathology | Xanthine Dehydrogenase - antagonists & inhibitors | Zinc - metabolism | Humans | Xanthine Dehydrogenase - genetics | Drosophila Proteins - metabolism | Drosophila melanogaster - genetics | Malpighian Tubules - chemistry | Drosophila melanogaster - metabolism | Kidney - metabolism | Cation Transport Proteins - metabolism | Dietary Proteins - pharmacology | Cation Transport Proteins - genetics | Malpighian Tubules - drug effects | Drosophila Proteins - antagonists & inhibitors | Disease Models, Animal | X-Ray Absorption Spectroscopy | Gene Expression | Kidney - drug effects | Chelating Agents - pharmacology | Kidney Calculi - metabolism | Kidney Calculi - pathology | Ethylenediamines - pharmacology | Animals | Dogs | Allopurinol - pharmacology | Drosophila Proteins - genetics | Malpighian Tubules - pathology | Kidney Calculi - genetics | Kidney Calculi - prevention & control | RNA, Small Interfering - metabolism | Care and treatment | Drosophila | Fossilization | Diagnosis | Research | Risk factors | Zinc | Kidney stones | Calcification (ectopic) | Dehydrogenases | Disease | Xanthine dehydrogenase | Biology | Hydroxyapatite | Stone | Urology | Etiology | Mineralization | Rodents | Atherosclerosis | Aging | Physiology | Inhibition | Plaques | Spectroscopy | Kidneys | Pharmacology | Xanthine | Metabolism | Zinc transporter | Diet | Insects | Arteriosclerosis | Calcification | Lithiasis | Trace elements | Mutation | Transporter | Kidney transplantation
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 10/2016, Volume 99, pp. 472 - 484
Xanthine oxidoreductase (XOR) is generally known as the final enzyme in purine metabolism and as a source of reactive oxygen species (ROS). In addition, this...
Hypertension | Oxidative stress | Endothelial nitric oxide synthase | Reactive oxygen species | Nitrate | Febuxostat | Nitric oxide | Xanthine oxidoreductase | Xanthine oxidase | Superoxide | Nitrite | Uric acid | NADPH OXIDASE | METABOLIC SYNDROME | OXIDASE INHIBITOR FEBUXOSTAT | BIOCHEMISTRY & MOLECULAR BIOLOGY | BLOOD-PRESSURE | REACTIVE SPECIES GENERATION | INDUCED HYPERTENSION | SYNTHASE ACTIVITY | ENDOCRINOLOGY & METABOLISM | DIETARY INORGANIC NITRATE | Xanthine Dehydrogenase - metabolism | Xanthine Dehydrogenase - antagonists & inhibitors | Xanthine Dehydrogenase - genetics | Nitrates - pharmacology | Male | Nitric Oxide Synthase Type III - deficiency | Febuxostat - pharmacology | Nitric Oxide Synthase Type II - antagonists & inhibitors | Nitric Oxide Synthase Type I - antagonists & inhibitors | Nitrites - blood | Superoxides - metabolism | Blood Pressure - drug effects | NG-Nitroarginine Methyl Ester - pharmacology | Nitrates - blood | Nitric Oxide - blood | Oxidation-Reduction | Signal Transduction | Nitric Oxide Synthase Type II - deficiency | Enzyme Inhibitors - pharmacology | Gene Expression Regulation | Nitric Oxide Synthase Type III - genetics | Nitrites - pharmacology | Mice, Knockout | Nitric Oxide Synthase Type I - deficiency | Nitric Oxide Synthase Type III - antagonists & inhibitors | Animals | Nitric Oxide Synthase Type II - genetics | Mice | Nitric Oxide Synthase Type I - genetics | Oxidases | Iron compounds | Homeostasis | Biological Sciences | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Cell Biology | Clinical Medicine | Naturvetenskap | Endokrinologi och diabetes | Biologiska vetenskaper | Natural Sciences | Cellbiologi | Endocrinology and Diabetes
Hypertension | Oxidative stress | Endothelial nitric oxide synthase | Reactive oxygen species | Nitrate | Febuxostat | Nitric oxide | Xanthine oxidoreductase | Xanthine oxidase | Superoxide | Nitrite | Uric acid | NADPH OXIDASE | METABOLIC SYNDROME | OXIDASE INHIBITOR FEBUXOSTAT | BIOCHEMISTRY & MOLECULAR BIOLOGY | BLOOD-PRESSURE | REACTIVE SPECIES GENERATION | INDUCED HYPERTENSION | SYNTHASE ACTIVITY | ENDOCRINOLOGY & METABOLISM | DIETARY INORGANIC NITRATE | Xanthine Dehydrogenase - metabolism | Xanthine Dehydrogenase - antagonists & inhibitors | Xanthine Dehydrogenase - genetics | Nitrates - pharmacology | Male | Nitric Oxide Synthase Type III - deficiency | Febuxostat - pharmacology | Nitric Oxide Synthase Type II - antagonists & inhibitors | Nitric Oxide Synthase Type I - antagonists & inhibitors | Nitrites - blood | Superoxides - metabolism | Blood Pressure - drug effects | NG-Nitroarginine Methyl Ester - pharmacology | Nitrates - blood | Nitric Oxide - blood | Oxidation-Reduction | Signal Transduction | Nitric Oxide Synthase Type II - deficiency | Enzyme Inhibitors - pharmacology | Gene Expression Regulation | Nitric Oxide Synthase Type III - genetics | Nitrites - pharmacology | Mice, Knockout | Nitric Oxide Synthase Type I - deficiency | Nitric Oxide Synthase Type III - antagonists & inhibitors | Animals | Nitric Oxide Synthase Type II - genetics | Mice | Nitric Oxide Synthase Type I - genetics | Oxidases | Iron compounds | Homeostasis | Biological Sciences | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Cell Biology | Clinical Medicine | Naturvetenskap | Endokrinologi och diabetes | Biologiska vetenskaper | Natural Sciences | Cellbiologi | Endocrinology and Diabetes
Journal Article
Circulation Research, ISSN 0009-7330, 10/2008, Volume 103, Issue 9, pp. 957 - 964
Reduction of nitrite (NO2) provides a major source of nitric oxide (NO) in the circulation, especially in hypoxemic conditions. Our previous studies suggest...
Blood vessels | Hypoxia | Cardiovascular research | Nitric oxide | HEMOGLOBIN | hypoxia | nitric oxide | OXIDATIVE STRESS | CARDIAC & CARDIOVASCULAR SYSTEMS | blood vessels | INDUCED VASODILATION | cardiovascular research | ISCHEMIA-REPERFUSION INJURY | IN-VIVO | S-NITROSOTHIOLS | MEDIATED DECOMPOSITION | PERIPHERAL VASCULAR DISEASE | RED-BLOOD-CELLS | REDUCES NITRITE | HEMATOLOGY | Xanthine Dehydrogenase - metabolism | Rats, Wistar | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Nitrites - metabolism | Male | omega-N-Methylarginine - pharmacology | Fluorometry | Cell Hypoxia | Nitrite Reductases - antagonists & inhibitors | Nitrites - blood | Erythrocytes - enzymology | Nitric Oxide Synthase Type III - metabolism | Aorta - enzymology | NG-Nitroarginine Methyl Ester - pharmacology | Nitric Oxide - blood | Oxidation-Reduction | Cells, Cultured | Enzyme Inhibitors - pharmacology | Rats | Xanthine Dehydrogenase - blood | Erythrocytes - drug effects | Nitric Oxide Synthase Type III - antagonists & inhibitors | Xanthine - metabolism | Nitric Oxide Synthase Type III - blood | Animals | Allopurinol - pharmacology | Nitric Oxide - metabolism | Endothelial Cells - enzymology | Arginine - metabolism | Endothelial Cells - drug effects | Hydrogen-Ion Concentration | Nitric Oxide Synthase Type II - metabolism | Nitrite Reductases - metabolism
Blood vessels | Hypoxia | Cardiovascular research | Nitric oxide | HEMOGLOBIN | hypoxia | nitric oxide | OXIDATIVE STRESS | CARDIAC & CARDIOVASCULAR SYSTEMS | blood vessels | INDUCED VASODILATION | cardiovascular research | ISCHEMIA-REPERFUSION INJURY | IN-VIVO | S-NITROSOTHIOLS | MEDIATED DECOMPOSITION | PERIPHERAL VASCULAR DISEASE | RED-BLOOD-CELLS | REDUCES NITRITE | HEMATOLOGY | Xanthine Dehydrogenase - metabolism | Rats, Wistar | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Nitrites - metabolism | Male | omega-N-Methylarginine - pharmacology | Fluorometry | Cell Hypoxia | Nitrite Reductases - antagonists & inhibitors | Nitrites - blood | Erythrocytes - enzymology | Nitric Oxide Synthase Type III - metabolism | Aorta - enzymology | NG-Nitroarginine Methyl Ester - pharmacology | Nitric Oxide - blood | Oxidation-Reduction | Cells, Cultured | Enzyme Inhibitors - pharmacology | Rats | Xanthine Dehydrogenase - blood | Erythrocytes - drug effects | Nitric Oxide Synthase Type III - antagonists & inhibitors | Xanthine - metabolism | Nitric Oxide Synthase Type III - blood | Animals | Allopurinol - pharmacology | Nitric Oxide - metabolism | Endothelial Cells - enzymology | Arginine - metabolism | Endothelial Cells - drug effects | Hydrogen-Ion Concentration | Nitric Oxide Synthase Type II - metabolism | Nitrite Reductases - metabolism
Journal Article
Journal of Pharmacology and Experimental Therapeutics, ISSN 0022-3565, 01/2011, Volume 336, Issue 1, pp. 95 - 103
4-[5-(Pyridin-4-yl)-1H-1,2,4-triazol-3-yl]pyridine-2-carbonitrile (FYX-051) is a potent inhibitor of bovine milk xanthine oxidoreductase (XOR). Steady-state...
ALLOPURINOL | TEI-6720 | ACID | MECHANISM | CRYSTAL-STRUCTURE | PURIFICATION | OXIDASE INHIBITOR | PHARMACOLOGY & PHARMACY | DEHYDROGENASE | Xanthine Dehydrogenase - metabolism | Nitriles - pharmacology | Rats, Wistar | Pyridines - chemistry | Xanthine Dehydrogenase - antagonists & inhibitors | Rats | Crystallography, X-Ray | Male | Structure-Activity Relationship | Binding, Competitive - drug effects | Animals | Cattle | Nitriles - chemistry | Xanthine Dehydrogenase - isolation & purification | Pyridines - pharmacology
ALLOPURINOL | TEI-6720 | ACID | MECHANISM | CRYSTAL-STRUCTURE | PURIFICATION | OXIDASE INHIBITOR | PHARMACOLOGY & PHARMACY | DEHYDROGENASE | Xanthine Dehydrogenase - metabolism | Nitriles - pharmacology | Rats, Wistar | Pyridines - chemistry | Xanthine Dehydrogenase - antagonists & inhibitors | Rats | Crystallography, X-Ray | Male | Structure-Activity Relationship | Binding, Competitive - drug effects | Animals | Cattle | Nitriles - chemistry | Xanthine Dehydrogenase - isolation & purification | Pyridines - pharmacology
Journal Article
British Journal of Pharmacology, ISSN 0007-1188, 07/2015, Volume 172, Issue 13, pp. 3341 - 3352
Background and Purpose Hypoxic conditions favour the reduction of nitrite to nitric oxide (NO) to elicit vasodilatation, but the mechanism(s) responsible for...
XANTHINE OXIDOREDUCTASE | OXIDE | CONCISE GUIDE | MECHANISM | PHARMACOLOGY | TOLERANCE | NITROGLYCERIN | PHARMACOLOGY & PHARMACY | DIETARY NITRATE | GLYCERYL TRINITRATE | BLOOD | Aldehyde Dehydrogenase - antagonists & inhibitors | Aldehyde Dehydrogenase, Mitochondrial | Humans | Middle Aged | Heart Failure - physiopathology | Male | Nitroglycerin - pharmacology | Aldehyde Dehydrogenase - physiology | Regional Blood Flow - drug effects | Arteries - physiology | Aldehydes - pharmacology | Forearm - blood supply | Female | Nitric Oxide Donors - pharmacology | Vasodilation - physiology | Spermine - analogs & derivatives | Vasodilator Agents - pharmacology | Mitochondrial Proteins - antagonists & inhibitors | Mitochondrial Proteins - physiology | Arteries - drug effects | Nitrites - pharmacology | Rats, Sprague-Dawley | Animals | Spermine - pharmacology | Hypoxia - physiopathology | Aged | Cyanamide - pharmacology | In Vitro Techniques | Heart failure | Heart | Dilatation | Vasodilators | Nitric oxide | Blood vessels | Nitrates | Aldehydes | Hypoxia | Coronary vessels | Dehydrogenases | Research Papers
XANTHINE OXIDOREDUCTASE | OXIDE | CONCISE GUIDE | MECHANISM | PHARMACOLOGY | TOLERANCE | NITROGLYCERIN | PHARMACOLOGY & PHARMACY | DIETARY NITRATE | GLYCERYL TRINITRATE | BLOOD | Aldehyde Dehydrogenase - antagonists & inhibitors | Aldehyde Dehydrogenase, Mitochondrial | Humans | Middle Aged | Heart Failure - physiopathology | Male | Nitroglycerin - pharmacology | Aldehyde Dehydrogenase - physiology | Regional Blood Flow - drug effects | Arteries - physiology | Aldehydes - pharmacology | Forearm - blood supply | Female | Nitric Oxide Donors - pharmacology | Vasodilation - physiology | Spermine - analogs & derivatives | Vasodilator Agents - pharmacology | Mitochondrial Proteins - antagonists & inhibitors | Mitochondrial Proteins - physiology | Arteries - drug effects | Nitrites - pharmacology | Rats, Sprague-Dawley | Animals | Spermine - pharmacology | Hypoxia - physiopathology | Aged | Cyanamide - pharmacology | In Vitro Techniques | Heart failure | Heart | Dilatation | Vasodilators | Nitric oxide | Blood vessels | Nitrates | Aldehydes | Hypoxia | Coronary vessels | Dehydrogenases | Research Papers
Journal Article
10.
Full Text
Hyperuricemia-related diseases and xanthine oxidoreductase (XOR) inhibitors: An overview
Medical Science Monitor, ISSN 1234-1010, 07/2016, Volume 22, pp. 2501 - 2512
Uric acid is the final oxidation product of purine metabolism in humans. Xanthine oxidoreductase (XOR) catalyzes oxidative hydroxylation of hypoxanthine to...
Cardiovascular diseases | Hyperuricemia | Gout | MEDICINE, RESEARCH & EXPERIMENTAL | Cardiovascular Diseases | OXIDASE INHIBITORS | TOXIC EPIDERMAL NECROLYSIS | SERUM URIC-ACID | DOSE-RESPONSE METAANALYSIS | ALL-CAUSE MORTALITY | GENERAL-POPULATION | NITRIC-OXIDE | DOUBLE-BLIND | DRUG-DELIVERY SYSTEMS | STEVENS-JOHNSON-SYNDROME | Xanthine Dehydrogenase - metabolism | Animals | Reactive Oxygen Species - metabolism | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Risk Factors | Enzyme Inhibitors - pharmacology | Allopurinol - pharmacology | Hyperuricemia - therapy | Enzyme Inhibitors - therapeutic use | Hyperuricemia - enzymology | Febuxostat - pharmacology
Cardiovascular diseases | Hyperuricemia | Gout | MEDICINE, RESEARCH & EXPERIMENTAL | Cardiovascular Diseases | OXIDASE INHIBITORS | TOXIC EPIDERMAL NECROLYSIS | SERUM URIC-ACID | DOSE-RESPONSE METAANALYSIS | ALL-CAUSE MORTALITY | GENERAL-POPULATION | NITRIC-OXIDE | DOUBLE-BLIND | DRUG-DELIVERY SYSTEMS | STEVENS-JOHNSON-SYNDROME | Xanthine Dehydrogenase - metabolism | Animals | Reactive Oxygen Species - metabolism | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Risk Factors | Enzyme Inhibitors - pharmacology | Allopurinol - pharmacology | Hyperuricemia - therapy | Enzyme Inhibitors - therapeutic use | Hyperuricemia - enzymology | Febuxostat - pharmacology
Journal Article
European Journal of Pharmacology, ISSN 0014-2999, 06/2016, Volume 780, pp. 224 - 231
Topiroxostat, a xanthine oxidoreductase (XOR) inhibitor, has been shown to decrease the urinary albumin-to-creatinine ratio compared with placebo in...
Diabetic nephropathy | Albuminuria | Topiroxostat | Xanthine oxidoreductase | Diabetic Nephropathies - urine | Diabetic Nephropathies - enzymology | Nitriles - pharmacology | Xanthine Dehydrogenase - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Pyridines - pharmacokinetics | Male | Diabetic Nephropathies - blood | Xanthine Dehydrogenase - blood | Nitriles - pharmacokinetics | Febuxostat - pharmacology | Animals | Enzyme Inhibitors - pharmacokinetics | Febuxostat - pharmacokinetics | Mice | Pyridines - pharmacology | Albuminuria - urine | Alkaloids | Chronic kidney failure | Analysis | Liver | Albumin | Xanthine | Uric acid | Diabetic nephropathies
Diabetic nephropathy | Albuminuria | Topiroxostat | Xanthine oxidoreductase | Diabetic Nephropathies - urine | Diabetic Nephropathies - enzymology | Nitriles - pharmacology | Xanthine Dehydrogenase - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Pyridines - pharmacokinetics | Male | Diabetic Nephropathies - blood | Xanthine Dehydrogenase - blood | Nitriles - pharmacokinetics | Febuxostat - pharmacology | Animals | Enzyme Inhibitors - pharmacokinetics | Febuxostat - pharmacokinetics | Mice | Pyridines - pharmacology | Albuminuria - urine | Alkaloids | Chronic kidney failure | Analysis | Liver | Albumin | Xanthine | Uric acid | Diabetic nephropathies
Journal Article
International Journal of Cardiology, ISSN 0167-5273, 2015, Volume 213, pp. 23 - 27
Abstract Hyperuricemia has long been established as the major etiologic factor in gout. Alongside with an inflammatory state triggered by urate crystal...
Cardiovascular | Oxidative stress | Hyperuricemia | Xanthine oxidase inhibitors | CARDIAC & CARDIOVASCULAR SYSTEMS | MANAGEMENT | GOUT | OXIDOREDUCTASE | FEBUXOSTAT | ALLOPURINOL | HEART | COLCHICINE | INFLAMMATION | CARDIOVASCULAR-DISEASE | XANTHINE-OXIDASE INHIBITION | Gout Suppressants - therapeutic use | Uric Acid - metabolism | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Enzyme Inhibitors - pharmacology | Oxidative Stress - drug effects | Enzyme Inhibitors - therapeutic use | Hyperuricemia - drug therapy | Heart failure | Hypertension | Enzymes | Care and treatment | Physiological aspects | Uric acid | Oxidases | Iron compounds | Safety and security measures | Food
Cardiovascular | Oxidative stress | Hyperuricemia | Xanthine oxidase inhibitors | CARDIAC & CARDIOVASCULAR SYSTEMS | MANAGEMENT | GOUT | OXIDOREDUCTASE | FEBUXOSTAT | ALLOPURINOL | HEART | COLCHICINE | INFLAMMATION | CARDIOVASCULAR-DISEASE | XANTHINE-OXIDASE INHIBITION | Gout Suppressants - therapeutic use | Uric Acid - metabolism | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Enzyme Inhibitors - pharmacology | Oxidative Stress - drug effects | Enzyme Inhibitors - therapeutic use | Hyperuricemia - drug therapy | Heart failure | Hypertension | Enzymes | Care and treatment | Physiological aspects | Uric acid | Oxidases | Iron compounds | Safety and security measures | Food
Journal Article
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 02/2012, Volume 32, Issue 2, pp. 291 - 298
OBJECTIVE—Hyperuricemia is common in patients with metabolic syndrome. We investigated the role of xanthine oxidoreductase (XOR) in atherosclerosis...
atherosclerosis | macrophages | xanthine oxidoreductase | cytokines | cell physiology | METABOLIC SYNDROME | MYOCARDIAL-INFARCTION | HIGH-FAT DIET | SERUM URIC-ACID | APOLIPOPROTEIN-E | PERCUTANEOUS CORONARY INTERVENTION | OXIDASE | PPAR-GAMMA | PERIPHERAL VASCULAR DISEASE | ANIMAL-MODEL | HEMATOLOGY | TRANSGENIC MICE | ATP Binding Cassette Transporter, Sub-Family G, Member 1 | Apolipoproteins E - deficiency | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Foam Cells - drug effects | Lipoproteins - metabolism | ATP-Binding Cassette Transporters - metabolism | ATP Binding Cassette Transporter 1 | Cell Differentiation - physiology | Foam Cells - pathology | Foam Cells - metabolism | Disease Models, Animal | Xanthine Dehydrogenase - drug effects | Cytokines - metabolism | Macrophages - pathology | Atherosclerosis - physiopathology | Cells, Cultured | Enzyme Inhibitors - pharmacology | Atherosclerosis - metabolism | Mice, Knockout | Macrophages - metabolism | Animals | Xanthine Dehydrogenase - physiology | Apolipoproteins E - genetics | Lipid Metabolism - drug effects | Allopurinol - pharmacology | Macrophages - drug effects | Mice
atherosclerosis | macrophages | xanthine oxidoreductase | cytokines | cell physiology | METABOLIC SYNDROME | MYOCARDIAL-INFARCTION | HIGH-FAT DIET | SERUM URIC-ACID | APOLIPOPROTEIN-E | PERCUTANEOUS CORONARY INTERVENTION | OXIDASE | PPAR-GAMMA | PERIPHERAL VASCULAR DISEASE | ANIMAL-MODEL | HEMATOLOGY | TRANSGENIC MICE | ATP Binding Cassette Transporter, Sub-Family G, Member 1 | Apolipoproteins E - deficiency | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Foam Cells - drug effects | Lipoproteins - metabolism | ATP-Binding Cassette Transporters - metabolism | ATP Binding Cassette Transporter 1 | Cell Differentiation - physiology | Foam Cells - pathology | Foam Cells - metabolism | Disease Models, Animal | Xanthine Dehydrogenase - drug effects | Cytokines - metabolism | Macrophages - pathology | Atherosclerosis - physiopathology | Cells, Cultured | Enzyme Inhibitors - pharmacology | Atherosclerosis - metabolism | Mice, Knockout | Macrophages - metabolism | Animals | Xanthine Dehydrogenase - physiology | Apolipoproteins E - genetics | Lipid Metabolism - drug effects | Allopurinol - pharmacology | Macrophages - drug effects | Mice
Journal Article
Drug Metabolism and Pharmacokinetics, ISSN 1347-4367, 02/2018, Volume 33, Issue 1, pp. 77 - 81
Hyperuricemia induces gout and kidney stones and accelerates the progression of renal and cardiovascular diseases. Adenosine 5′-triphosphate-binding cassette...
Hyperuricemia therapy | Oxypurinol | Febuxostat | Allopurinol | A serum uric acid lowering drug | GOUT | RESISTANCE PROTEIN TRANSPORTER | RISK | LOCI | BCRP/ABCG2 | PHARMACOKINETICS | KIDNEY-FUNCTION | PHARMACOLOGY & PHARMACY | URIC-ACID | GENOME-WIDE ASSOCIATION | Xanthine Dehydrogenase - metabolism | Oxypurinol - metabolism | Enzyme Inhibitors - metabolism | ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Hyperuricemia - metabolism | Neoplasm Proteins - metabolism | Hep G2 Cells | HEK293 Cells | Biological Transport - physiology | Cell Membrane - metabolism | Allopurinol - metabolism
Hyperuricemia therapy | Oxypurinol | Febuxostat | Allopurinol | A serum uric acid lowering drug | GOUT | RESISTANCE PROTEIN TRANSPORTER | RISK | LOCI | BCRP/ABCG2 | PHARMACOKINETICS | KIDNEY-FUNCTION | PHARMACOLOGY & PHARMACY | URIC-ACID | GENOME-WIDE ASSOCIATION | Xanthine Dehydrogenase - metabolism | Oxypurinol - metabolism | Enzyme Inhibitors - metabolism | ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism | Xanthine Dehydrogenase - antagonists & inhibitors | Humans | Hyperuricemia - metabolism | Neoplasm Proteins - metabolism | Hep G2 Cells | HEK293 Cells | Biological Transport - physiology | Cell Membrane - metabolism | Allopurinol - metabolism
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2003, Volume 278, Issue 3, pp. 1848 - 1855
TEI-6720 (2-(3-cyano-4-isobutoxyphenyl)-4-methyl-5thiazolecarboxylic acid) is an extremely potent inhibitor of xanthine oxidoreductase. Steady state kinetics...
RAT-LIVER | DEHYDROGENASE TYPE | ALLOPURINOL | OXYGEN | PROTEIN | BOVINE-MILK | CONVERSION | BIOCHEMISTRY & MOLECULAR BIOLOGY | PURIFICATION | ELECTRON-DENSITY MAPS | OXIDASE INHIBITOR | Milk - enzymology | Febuxostat | Xanthine Dehydrogenase - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Models, Molecular | Spectrometry, Fluorescence | Crystallography, X-Ray | Animals | Cattle | Enzyme Inhibitors - chemistry | Thiazoles - chemistry | Molecular Structure | Thiazoles - pharmacology | Kinetics | Xanthine Dehydrogenase - chemistry
RAT-LIVER | DEHYDROGENASE TYPE | ALLOPURINOL | OXYGEN | PROTEIN | BOVINE-MILK | CONVERSION | BIOCHEMISTRY & MOLECULAR BIOLOGY | PURIFICATION | ELECTRON-DENSITY MAPS | OXIDASE INHIBITOR | Milk - enzymology | Febuxostat | Xanthine Dehydrogenase - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Models, Molecular | Spectrometry, Fluorescence | Crystallography, X-Ray | Animals | Cattle | Enzyme Inhibitors - chemistry | Thiazoles - chemistry | Molecular Structure | Thiazoles - pharmacology | Kinetics | Xanthine Dehydrogenase - chemistry
Journal Article