9,10-epoxy-9,10-dihydrophenanthrene has been researched along with phenanthrenes in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (40.00) | 18.7374 |
| 1990's | 3 (30.00) | 18.2507 |
| 2000's | 1 (10.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Blum, J; Lifshitz, Y; Sheradsky, T; Shtelzer, S; Stark, AA; Zeiger, E | 1 |
| Blum, J; Glatt, H; Oesch, F; Sheradsky, T; Shtelzer, S | 1 |
| Parfenov, EA; Serdiuk, OA; Sotnichenko, AI; Starovoĭtov, ML; Sukhanov, VA | 1 |
| Armstrong, RN; Shan, S | 1 |
| Armstrong, RN; Edwards, GH; Lacourciere, GM; Moos, M; Morris, DI; Tan, CP; Vakharia, VN | 1 |
| Armstrong, RN; Gilliland, GL; Ji, X; Johnson, WW; Liu, S | 1 |
| Mulholland, AJ; Ridder, L; Rietjens, IM; Vervoort, J | 1 |
| BOYLAND, E; SIMS, P | 1 |
| Arand, M; Bockamp, E; Haenel, K; Heck, R; Kindler, D; Marowsky, A; Mule, N; Rudin, M; Rutishauser, S | 1 |
| Bano, A; Habiba, U; Khan, BA; Khan, F; Khan, NN; Niazi, MBK; Uzair, B | 1 |
10 other study(ies) available for 9,10-epoxy-9,10-dihydrophenanthrene and phenanthrenes
| Article | Year |
|---|---|
Structure-activity relationships in the mutagenicity of N-substituted derivatives of phenanthrene-9,10-imine.
Topics: Alkylating Agents; Alkylation; Dose-Response Relationship, Drug; Mutagenicity Tests; Mutagens; Phenanthrenes; Salmonella typhimurium; Structure-Activity Relationship | 1986 |
Mutagenicity of N-substituted phenanthrene 9,10-imines in Salmonella typhimurium and Chinese hamster V79 cells.
Topics: Animals; Aziridines; Azirines; Cell Line; Cricetinae; Cricetulus; Mutagenicity Tests; Mutagens; Phenanthrenes; Salmonella typhimurium; Structure-Activity Relationship | 1986 |
[Chromatographic method of determining membrane epoxide hydrolase activity].
Topics: Animals; Chromatography, High Pressure Liquid; Epoxide Hydrolases; Intracellular Membranes; Male; Microsomes, Liver; Phenanthrenes; Rats; Rats, Inbred Strains; Substrate Specificity | 1985 |
Rational reconstruction of the active site of a class mu glutathione S-transferase.
Topics: Animals; Binding Sites; Butanones; Epoxy Compounds; Glutathione Transferase; Isoenzymes; Kinetics; Mutation; Phenanthrenes; Rats; Substrate Specificity | 1994 |
Interaction of hepatic microsomal epoxide hydrolase derived from a recombinant baculovirus expression system with an azarene oxide and an aziridine substrate analogue.
Topics: Animals; Baculoviridae; Cell Line; Chromatography; Chromatography, DEAE-Cellulose; Cloning, Molecular; Durapatite; Electrophoresis, Polyacrylamide Gel; Epoxide Hydrolases; Genetic Vectors; Hydroxyapatites; Insecta; Kinetics; Mathematics; Microsomes, Liver; Molecular Weight; Moths; Phenanthrenes; Phenanthrolines; Recombinant Proteins; Restriction Mapping; Substrate Specificity; Transfection | 1993 |
Tyrosine 115 participates both in chemical and physical steps of the catalytic mechanism of a glutathione S-transferase.
Topics: Amino Acid Sequence; Dinitrochlorobenzene; Glutathione; Glutathione Transferase; Hydrogen Bonding; Isoenzymes; Kinetics; Models, Molecular; Mutagenesis, Site-Directed; Phenanthrenes; Polymerase Chain Reaction; Protein Conformation; Protein Structure, Secondary; Recombinant Proteins; Tyrosine; Viscosity; X-Ray Diffraction | 1993 |
Quantum mechanical/molecular mechanical free energy simulations of the glutathione S-transferase (M1-1) reaction with phenanthrene 9,10-oxide.
Topics: Binding Sites; Computer Simulation; Glutathione Transferase; Hydrogen Bonding; Models, Chemical; Models, Molecular; Mutation; Phenanthrenes; Quantum Theory; Thermodynamics | 2002 |
METABOLISM OF POLYCYCLIC COMPOUNDS. THE METABOLISM OF 9,10-EPOXY-9,10-DIHYDROPHENANTHRENE IN RATS.
Topics: Acetylcysteine; Animals; Chromatography; Cysteine; Epoxy Compounds; Ethers; Ethers, Cyclic; Glutathione; Metabolism; Phenanthrenes; Polycyclic Compounds; Rabbits; Rats; Research | 1965 |
Genetic enhancement of microsomal epoxide hydrolase improves metabolic detoxification but impairs cerebral blood flow regulation.
Topics: Amino Acid Substitution; Animals; Catalytic Domain; Cerebral Cortex; Cerebrovascular Circulation; Cerebrovascular Disorders; Eicosanoids; Epoxide Hydrolases; Hippocampus; Inactivation, Metabolic; Mice; Mice, Mutant Strains; Microsomes, Liver; Neurons; Phenanthrenes; Point Mutation; Vascular Resistance; Vasodilation; Vasodilator Agents; Xenobiotics | 2016 |
In vitro antifungal activity of 9, 10-dihydrophenanthrene-2-carboxylic acid isolated from a marine bacterium: Pseudomonas putida.
Topics: Animals; Antifungal Agents; Candida albicans; Carboxylic Acids; Humans; Microbial Sensitivity Tests; Phenanthrenes; Pseudomonas putida | 2018 |