Page last updated: 2024-08-23

selegiline and oxepins

selegiline has been researched along with oxepins in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (22.22)18.2507
2000's7 (77.78)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Furst, P; Kragten, E; Lalande, I; Muller, D; Roggo, S; Schindler, P; van Oostrum, J; Waldmeier, P; Zimmermann, K1
Fürst, P; Kragten, E; Roggo, S; Waldmeier, P; Zimmermann, K1
Borden, KE; Carlile, GW; Chalmers-Redman, RM; Pong, A; Tatton, NA; Tatton, WG1
Hengerer, B; Spooren, WP; Waldmeier, PC1
Boulton, AA; Cools, AR; Kato, AC; Tatton, WG; Waldmeier, PC1
Jenner, P1
LeWitt, PA1
Drinkwater, D; Ji, Q; Liu, F; Pan, C; Vivilecchia, R; Wang, W1
Bae, BI; Cascio, MB; Dawson, TM; Dawson, VL; Hara, MR; Hester, LD; Sawa, A; Snyder, SH; Thomas, B1

Reviews

2 review(s) available for selegiline and oxepins

ArticleYear
Preclinical evidence for neuroprotection with monoamine oxidase-B inhibitors in Parkinson's disease.
    Neurology, 2004, Oct-12, Volume: 63, Issue:7 Suppl 2

    Topics: Amphetamines; Animals; Antiparkinson Agents; Apoptosis; Clinical Trials as Topic; Drug Evaluation, Preclinical; Haplorhini; Humans; Inactivation, Metabolic; Indans; Mice; Mice, Transgenic; Models, Neurological; Monoamine Oxidase Inhibitors; Neurons; Neuroprotective Agents; Oxepins; Oxidative Stress; Pargyline; Parkinson Disease; Propylamines; Selegiline

2004
Clinical trials of neuroprotection for Parkinson's disease.
    Neurology, 2004, Oct-12, Volume: 63, Issue:7 Suppl 2

    Topics: Antiparkinson Agents; Clinical Trials as Topic; Creatine; Dopamine Agonists; Double-Blind Method; Humans; Indans; Minocycline; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Multicenter Studies as Topic; Nerve Tissue Proteins; Neuroprotective Agents; Oxepins; Parkinson Disease; Picolinic Acids; Randomized Controlled Trials as Topic; Riluzole; Selegiline; Ubiquinone

2004

Other Studies

7 other study(ies) available for selegiline and oxepins

ArticleYear
Glyceraldehyde-3-phosphate dehydrogenase, the putative target of the antiapoptotic compounds CGP 3466 and R-(-)-deprenyl.
    The Journal of biological chemistry, 1998, Mar-06, Volume: 273, Issue:10

    Topics: Animals; Antiparkinson Agents; Apoptosis; Biosensing Techniques; Brain; Cell Line; Gene Expression Regulation; Glyceraldehyde-3-Phosphate Dehydrogenases; Humans; Microscopy, Fluorescence; Molecular Structure; Muscles; Neuroblastoma; Neuroprotective Agents; Oligonucleotides, Antisense; Oxepins; Parkinson Disease; Photoaffinity Labels; Propylamines; Protein Binding; Rabbits; Rats; Selegiline

1998
Synthesis of tools for target identification of the anti-apoptotic compound CGP 3466; Part I.
    Bioorganic & medicinal chemistry letters, 1998, May-19, Volume: 8, Issue:10

    Topics: Animals; Apoptosis; Chromatography, Affinity; Fluorescent Dyes; Hippocampus; Indicators and Reagents; Molecular Structure; Neurons; Neuroprotective Agents; Oxepins; Rats; Selegiline; Structure-Activity Relationship

1998
Reduced apoptosis after nerve growth factor and serum withdrawal: conversion of tetrameric glyceraldehyde-3-phosphate dehydrogenase to a dimer.
    Molecular pharmacology, 2000, Volume: 57, Issue:1

    Topics: Amphetamines; Animals; Apoptosis; Blood Proteins; Dimerization; Glyceraldehyde-3-Phosphate Dehydrogenases; Monoamine Oxidase Inhibitors; Nerve Growth Factor; Oxepins; PC12 Cells; Protein Conformation; Rats; Selegiline

2000
CGP 3466 protects dopaminergic neurons in lesion models of Parkinson's disease.
    Naunyn-Schmiedeberg's archives of pharmacology, 2000, Volume: 362, Issue:6

    Topics: 1-Methyl-4-phenylpyridinium; Animals; Antiparkinson Agents; Brain; Cell Culture Techniques; Cell Death; Disease Models, Animal; Dopamine; Female; Liver; Mesencephalon; Mice; Mice, Inbred C57BL; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Neurons; Oxepins; Oxidopamine; Parkinsonian Disorders; Pregnancy; Rats; Selegiline; Substantia Nigra; Tritium; Tyrosine 3-Monooxygenase

2000
Neurorescuing effects of the GAPDH ligand CGP 3466B.
    Journal of neural transmission. Supplementum, 2000, Issue:60

    Topics: Animals; Animals, Newborn; Brain; Cell Survival; Cells, Cultured; Disease Models, Animal; Glyceraldehyde-3-Phosphate Dehydrogenases; Ligands; Mice; Mice, Inbred C57BL; Neurons; Neuroprotective Agents; Oxepins; Parkinson Disease; Rats; Rats, Wistar; Selegiline

2000
The use of LC/MS, GC/MS, and LC/NMR hyphenated techniques to identify a drug degradation product in pharmaceutical development.
    Journal of pharmaceutical and biomedical analysis, 2006, Feb-24, Volume: 40, Issue:3

    Topics: Chromatography, Liquid; Drug Contamination; Gas Chromatography-Mass Spectrometry; Magnetic Resonance Spectroscopy; Mass Spectrometry; Oxepins; Pharmaceutical Preparations; Selegiline; Stereoisomerism

2006
Neuroprotection by pharmacologic blockade of the GAPDH death cascade.
    Proceedings of the National Academy of Sciences of the United States of America, 2006, Mar-07, Volume: 103, Issue:10

    Topics: Animals; Antiparkinson Agents; Apoptosis; Cell Line; Glyceraldehyde-3-Phosphate Dehydrogenases; Humans; In Vitro Techniques; Male; Mice; MPTP Poisoning; Nerve Degeneration; Neuroprotective Agents; Nitric Oxide; Nuclear Proteins; Oxepins; Parkinson Disease; Selegiline; Ubiquitin-Protein Ligases

2006