alpha-naphthoflavone has been researched along with phenacetin in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (18.18) | 18.7374 |
| 1990's | 4 (36.36) | 18.2507 |
| 2000's | 2 (18.18) | 29.6817 |
| 2010's | 2 (18.18) | 24.3611 |
| 2020's | 1 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| Dai, R; Liu, Y; She, M; Wu, Z | 1 |
| Guo, HF; Jin, J; Li, ZR; Liu, ZY; Xie, ZS; Xue, ST; Yi, H; Zhang, L | 1 |
| Beaune, PH; Bercovici, JP; Berthou, F; Dreano, Y; Floch, HH; Kerlan, V | 1 |
| Lennard, MS; Loft, S; Otton, SV; Poulsen, HE; Tucker, GT | 1 |
| Borm, PJ; Frankhuijzen-Sierevogel, A; Noordhoek, J | 1 |
| Chiba, K; Echizen, H; Ishizaki, T; Tani, M; Yoshimoto, K | 1 |
| Greenblatt, DJ; Venkatakrishnan, K; von Moltke, LL | 1 |
| Hu, YZ; Yao, TW | 1 |
| Kamimura, H; Noguchi, K; Tenmizu, D | 1 |
| Boobis, AR; Brodie, MJ; Davies, DS; Kahn, GC; Whyte, C | 1 |
| Adcock, JM; Daniels, JS; Locuson, CW; Williams, P | 1 |
11 other study(ies) available for alpha-naphthoflavone and phenacetin
| Article | Year |
|---|---|
The inhibition study of human UDP-glucuronosyltransferases with cytochrome P450 selective substrates and inhibitors.
Topics: Cytochrome P-450 Enzyme Inhibitors; Enzyme Activation; Enzyme Inhibitors; Glucuronosyltransferase; Humans; Molecular Structure; Recombinant Proteins; Stereoisomerism; Structure-Activity Relationship; Substrate Specificity | 2011 |
Substituted benzothiophene and benzofuran derivatives as a novel class of bone morphogenetic Protein-2 upregulators: Synthesis, anti-osteoporosis efficacies in ovariectomized rats and a zebrafish model, and ADME properties.
Topics: Animals; Benzofurans; Bone Morphogenetic Protein 2; Caco-2 Cells; Disease Models, Animal; Dose-Response Relationship, Drug; Humans; Mice; Mice, Inbred BALB C; Molecular Structure; Osteoporosis; Ovariectomy; Rats; Rats, Sprague-Dawley; Structure-Activity Relationship; Thiophenes; Zebrafish | 2020 |
Nature of cytochromes P450 involved in the 2-/4-hydroxylations of estradiol in human liver microsomes.
Topics: Adolescent; Adult; Benzoflavones; Caffeine; Child, Preschool; Cytochrome P-450 CYP1A2; Cytochrome P-450 Enzyme Inhibitors; Cytochrome P-450 Enzyme System; Enzyme Activation; Estradiol; Female; Humans; Hydroxylation; Infant; Infant, Newborn; Isoenzymes; Kinetics; Male; Microsomes, Liver; Middle Aged; Norpregnenes; Oxidoreductases; Phenacetin; Progesterone Congeners; Tamoxifen; Testosterone | 1992 |
Characterization of metronidazole metabolism by human liver microsomes.
Topics: Acetone; Adult; Benzoflavones; Caffeine; Cytochrome P-450 Enzyme Inhibitors; Humans; Hydroxylation; In Vitro Techniques; Kinetics; Male; Mephenytoin; Metronidazole; Microsomes, Liver; Middle Aged; Nifedipine; Phenacetin; Quinidine; Theophylline; Tolbutamide | 1991 |
Kinetics of in vitro O-deethylation of phenacetin and 7-ethoxycoumarin by rat intestinal mucosal cells and microsomes. The effect of induction with 3-methylcholanthrene and inhibition with alpha-naphthoflavone.
Topics: Animals; Benzoflavones; Chromatography, High Pressure Liquid; Coumarins; Cytochrome P-450 Enzyme System; Flavonoids; Humans; Intestinal Mucosa; Kinetics; Male; Methylcholanthrene; Mice; Microsomes; Phenacetin; Rats; Rats, Inbred Strains | 1983 |
Identification of human CYP isoforms involved in the metabolism of propranolol enantiomers--N-desisopropylation is mediated mainly by CYP1A2.
Topics: Aged; Benzoflavones; Cytochrome P-450 CYP3A; Cytochrome P-450 Enzyme Inhibitors; Cytochrome P-450 Enzyme System; Desipramine; Ditiocarb; Female; Humans; Hydroxylation; In Vitro Techniques; Isoenzymes; Male; Mephenytoin; Microsomes, Liver; Middle Aged; Oxazines; Phenacetin; Propranolol; Quinidine; Recombinant Proteins; Stereoisomerism; Substrate Specificity; Sulfaphenazole; Tolbutamide; Troleandomycin | 1995 |
Human cytochromes P450 mediating phenacetin O-deethylation in vitro: validation of the high affinity component as an index of CYP1A2 activity.
Topics: Benzoflavones; Cytochrome P-450 CYP1A2; Cytochrome P-450 Enzyme System; Humans; In Vitro Techniques; Microsomes, Liver; Omeprazole; Phenacetin; Protein Isoforms; Reproducibility of Results; Sulfaphenazole | 1998 |
Induction of diphenytriazol on cytochrome CYP1A.
Topics: Abortifacient Agents, Nonsteroidal; Aminopyrine; Animals; Benzoflavones; beta-Naphthoflavone; Cytochrome P-450 CYP1A1; Cytochrome P-450 CYP2B1; Female; Fluvoxamine; Microsomes, Liver; Phenacetin; Rats; Rats, Sprague-Dawley; Triazoles | 2004 |
Elucidation of the effects of the CYP1A2 deficiency polymorphism in the metabolism of 4-cyclohexyl-1-ethyl-7-methylpyrido[2,3-d]pyrimidine-2-(1h)-one (YM-64227), a phosphodiesterase type 4 inhibitor, and its metabolites in dogs.
Topics: 3',5'-Cyclic-AMP Phosphodiesterases; Animals; Antibodies, Monoclonal; Area Under Curve; Benzoflavones; Cyclic Nucleotide Phosphodiesterases, Type 4; Cyclohexanes; Cytochrome P-450 CYP1A2; Dogs; Genotype; In Vitro Techniques; Microsomes, Liver; Molecular Structure; Phenacetin; Polymorphism, Single Nucleotide; Pyrimidines | 2006 |
Biphasic O-deethylation of phenacetin and 7-ethoxycoumarin by human and rat liver microsomal fractions.
Topics: 7-Alkoxycoumarin O-Dealkylase; Animals; Benzoflavones; Coumarins; Cytochrome P-450 Enzyme System; Humans; Kinetics; Male; Metyrapone; Microsomes, Liver; Phenacetin; Rats; Rats, Wistar; Subcellular Fractions; Substrate Specificity | 1981 |
Evaluation of tizanidine as a marker of canine CYP1A2 activity.
Topics: Adrenergic alpha-2 Receptor Agonists; Animals; Benzoflavones; Clonidine; Cytochrome P-450 CYP1A2; Cytochrome P-450 CYP1A2 Inhibitors; Dogs; Enrofloxacin; Female; Fluoroquinolones; Microsomes, Liver; Molecular Probes; Phenacetin; Substrate Specificity; Theophylline | 2016 |