opromazine has been researched along with fluphenazine in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 2 (40.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Creveling, CR; Daly, JW; Lewandowski, GA; McNeal, ET | 1 |
| Chan, C; Croft, SL; Douglas, KT; Fairlamb, AH; Garforth, J; Jaouhari, R; McKie, JH; Rock, PJ; Speers, P; Yardley, V; Yin, H | 1 |
| Pajeva, I; Wiese, M | 1 |
| Cho, YS; Hwang, EM; Jung, SY; Lim, SM; Min, SJ; Pae, AN; Park, KD; Viswanath, AN | 1 |
| Minervini, N; Witman, GB | 1 |
5 other study(ies) available for opromazine and fluphenazine
| Article | Year |
|---|---|
[3H]Batrachotoxinin A 20 alpha-benzoate binding to voltage-sensitive sodium channels: a rapid and quantitative assay for local anesthetic activity in a variety of drugs.
Topics: Adrenergic alpha-Antagonists; Adrenergic beta-Antagonists; Anesthetics, Local; Animals; Batrachotoxins; Calcium Channel Blockers; Cyclic AMP; Guinea Pigs; Histamine H1 Antagonists; In Vitro Techniques; Ion Channels; Neurotoxins; Sodium; Tranquilizing Agents; Tritium | 1985 |
Phenothiazine inhibitors of trypanothione reductase as potential antitrypanosomal and antileishmanial drugs.
Topics: Animals; Antiprotozoal Agents; Binding Sites; Crithidia fasciculata; Enzyme Inhibitors; Glutathione Disulfide; Glutathione Reductase; Kinetics; Leishmania donovani; Models, Chemical; NADH, NADPH Oxidoreductases; NADP; Phenothiazines; Trypanocidal Agents; Trypanosoma brucei brucei; Trypanosoma cruzi | 1998 |
Molecular modeling of phenothiazines and related drugs as multidrug resistance modifiers: a comparative molecular field analysis study.
Topics: Antineoplastic Agents; Cell Survival; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; Humans; Models, Molecular; Molecular Conformation; Phenothiazines; Thioxanthenes; Tumor Cells, Cultured | 1998 |
Identification of the first in silico-designed TREK1 antagonists that block channel currents dose dependently.
Topics: Animals; Computer Simulation; Crystallography, X-Ray; Dose-Response Relationship, Drug; HEK293 Cells; Humans; Mice; Mice, Knockout; Molecular Docking Simulation; Potassium Channels, Tandem Pore Domain | 2016 |
Role of calmodulin in the flagellar axoneme: effect of phenothiazines on reactivated axonemes of Chlamydomonas.
Topics: 2',3'-Cyclic-Nucleotide Phosphodiesterases; Calcium; Calcium-Binding Proteins; Calmodulin; Chlamydomonas; Chlorpromazine; Flagella; Fluphenazine; Movement; Phenothiazines | 1982 |