doxorubicin hydrochloride and resveratrol

doxorubicin hydrochloride has been researched along with resveratrol 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	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Barnes, J; Bryce, RA; Caraher, MC; Doncaster, JR; Humphries, MP; Nolan, KA; Stratford, IJ; Tirelli, N; Whitehead, RC	1
Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P	1

Other Studies

2 other study(ies) available for doxorubicin hydrochloride and resveratrol

Article	Year
Triazoloacridin-6-ones as novel inhibitors of the quinone oxidoreductases NQO1 and NQO2. Bioorganic & medicinal chemistry, 2010, Jan-15, Volume: 18, Issue:2 Topics: Acridines; Animals; Cell Line, Tumor; Cell Proliferation; Crystallography, X-Ray; DNA; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Humans; Male; Models, Molecular; Molecular Structure; NAD(P)H Dehydrogenase (Quinone); Quinone Reductases; Salmon; Spermatozoa; Structure-Activity Relationship; Transition Temperature; Triazoles	2010
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

Article

Year

Triazoloacridin-6-ones as novel inhibitors of the quinone oxidoreductases NQO1 and NQO2.

Bioorganic & medicinal chemistry, 2010, Jan-15, Volume: 18, Issue:2

Topics: Acridines; Animals; Cell Line, Tumor; Cell Proliferation; Crystallography, X-Ray; DNA; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Humans; Male; Models, Molecular; Molecular Structure; NAD(P)H Dehydrogenase (Quinone); Quinone Reductases; Salmon; Spermatozoa; Structure-Activity Relationship; Transition Temperature; Triazoles

2010

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