Compounds > n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide

n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide and malondialdehyde

n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide has been researched along with malondialdehyde in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Boscá, L; Fernández, AP; Leza, JC; Lizasoain, I; Lorenzo, P; Madrigal, JL; Moro, MA; Rodrigo, J	1
Gupta, A; Kulkarni, SK; Kumar, A	1

Other Studies

2 other study(ies) available for n-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide and malondialdehyde

Article	Year
Induction of cyclooxygenase-2 accounts for restraint stress-induced oxidative status in rat brain. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2003, Volume: 28, Issue:9 Topics: Animals; Antioxidants; Blotting, Western; Brain; Brain Chemistry; Calcium; Cell Nucleus; Cell Size; Corticosterone; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxygenase Inhibitors; Cytosol; Dinoprostone; Dizocilpine Maleate; Drug Interactions; Electrophoretic Mobility Shift Assay; Glutathione; Immobilization; Immunohistochemistry; Isoenzymes; Male; Malondialdehyde; Neurons; Neuroprotective Agents; NF-kappa B; Nitric Oxide Synthase; Nitrobenzenes; Proline; Prostaglandin-Endoperoxide Synthases; Rats; Rats, Wistar; Stress, Physiological; Sulfonamides; Thiocarbamates; Time Factors	2003
Targeting oxidative stress, mitochondrial dysfunction and neuroinflammatory signaling by selective cyclooxygenase (COX)-2 inhibitors mitigates MPTP-induced neurotoxicity in mice. Progress in neuro-psychopharmacology & biological psychiatry, 2011, Jun-01, Volume: 35, Issue:4 Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Caspase 3; Catatonia; Cyclooxygenase 2 Inhibitors; Inflammation; Isoxazoles; Lipid Peroxidation; Male; Malondialdehyde; Mice; Mitochondria; Motor Activity; MPTP Poisoning; NADH Dehydrogenase; Neuroprotective Agents; Nitrites; Nitrobenzenes; Oxidative Stress; Signal Transduction; Sulfhydryl Compounds; Sulfonamides; Tetrazolium Salts; Thiazoles; Thiobarbituric Acid Reactive Substances; Transcription Factor RelA	2011

Article

Year

Induction of cyclooxygenase-2 accounts for restraint stress-induced oxidative status in rat brain.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2003, Volume: 28, Issue:9

Topics: Animals; Antioxidants; Blotting, Western; Brain; Brain Chemistry; Calcium; Cell Nucleus; Cell Size; Corticosterone; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxygenase Inhibitors; Cytosol; Dinoprostone; Dizocilpine Maleate; Drug Interactions; Electrophoretic Mobility Shift Assay; Glutathione; Immobilization; Immunohistochemistry; Isoenzymes; Male; Malondialdehyde; Neurons; Neuroprotective Agents; NF-kappa B; Nitric Oxide Synthase; Nitrobenzenes; Proline; Prostaglandin-Endoperoxide Synthases; Rats; Rats, Wistar; Stress, Physiological; Sulfonamides; Thiocarbamates; Time Factors

2003

Targeting oxidative stress, mitochondrial dysfunction and neuroinflammatory signaling by selective cyclooxygenase (COX)-2 inhibitors mitigates MPTP-induced neurotoxicity in mice.

Progress in neuro-psychopharmacology & biological psychiatry, 2011, Jun-01, Volume: 35, Issue:4

Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Caspase 3; Catatonia; Cyclooxygenase 2 Inhibitors; Inflammation; Isoxazoles; Lipid Peroxidation; Male; Malondialdehyde; Mice; Mitochondria; Motor Activity; MPTP Poisoning; NADH Dehydrogenase; Neuroprotective Agents; Nitrites; Nitrobenzenes; Oxidative Stress; Signal Transduction; Sulfhydryl Compounds; Sulfonamides; Tetrazolium Salts; Thiazoles; Thiobarbituric Acid Reactive Substances; Transcription Factor RelA

2011