2,3-dimethoxy-5-methyl-6-decyl-1,4-benzoquinone and cyclosporine

2,3-dimethoxy-5-methyl-6-decyl-1,4-benzoquinone has been researched along with cyclosporine in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P1
Bernardi, P; Fontaine, E; Ichas, F1
Hua, DH; Lou, K; Perchellet, EM; Perchellet, JP; Wang, Y; Ward, MM1
Barajas, M; Griffiths, KK; Homma, S; Levy, RJ; Liu, R; Matsumoto, K; Wang, A1

Other Studies

4 other study(ies) available for 2,3-dimethoxy-5-methyl-6-decyl-1,4-benzoquinone and cyclosporine

ArticleYear
Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.
    Bioorganic & medicinal chemistry, 2012, Nov-15, Volume: 20, Issue:22

    Topics: Acetylcholinesterase; Amyloid beta-Peptides; Benzophenanthridines; Binding Sites; Butyrylcholinesterase; Catalytic Domain; Cholinesterase Inhibitors; Humans; Isoquinolines; Kinetics; Molecular Docking Simulation; Structure-Activity Relationship

2012
A ubiquinone-binding site regulates the mitochondrial permeability transition pore.
    The Journal of biological chemistry, 1998, Oct-02, Volume: 273, Issue:40

    Topics: Animals; Arsenicals; Atractyloside; Binding Sites; Calcium; Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone; Cyclosporine; Intracellular Membranes; Ion Channels; Mitochondria, Liver; Molecular Structure; Permeability; Porins; Quinones; Rats; Ubiquinone

1998
Rapid collapse of mitochondrial transmembrane potential in HL-60 cells and isolated mitochondria treated with anti-tumor 1,4-anthracenediones.
    Anti-cancer drugs, 2005, Volume: 16, Issue:9

    Topics: Alamethicin; Animals; Anthraquinones; ATP Binding Cassette Transporter, Subfamily B, Member 1; Bongkrekic Acid; Calcium Chloride; Carbonyl Cyanide m-Chlorophenyl Hydrazone; Cyclosporine; Cysteine Proteinase Inhibitors; Daunorubicin; Dose-Response Relationship, Drug; Drug Resistance, Multiple; Female; Gramicidin; HL-60 Cells; Humans; Intracellular Membranes; Ion Channels; Membrane Potentials; Mice; Mitochondria; Mitochondrial Membrane Transport Proteins; Mitochondrial Permeability Transition Pore; Mitoxantrone; Ruthenium Red; Staurosporine; Ubiquinone

2005
The newborn Fmr1 knockout mouse: a novel model of excess ubiquinone and closed mitochondrial permeability transition pore in the developing heart.
    Pediatric research, 2021, Volume: 89, Issue:3

    Topics: Animals; Atractyloside; Cyclosporine; Disease Models, Animal; Electron Transport; Fetal Heart; Fragile X Mental Retardation Protein; Fragile X Syndrome; Guanosine Diphosphate; Male; Mice; Mice, Knockout; Mitochondria, Heart; Mitochondrial Permeability Transition Pore; Myocytes, Cardiac; Oxygen Consumption; Proton-Motive Force; Single-Blind Method; Ubiquinone

2021