lawsone has been researched along with dichlone in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dunn, WJ; Hodnett, EM; Marrs, P; Wongwiechintana, C | 1 |
| Douglas, KT; Guedes, RC; Iley, J; Jaffar, M; Moreira, R; Valente, C | 1 |
| Carroll, PJ; DuHadaway, JB; Jaller, D; Kumar, S; LaLonde, JM; Malachowski, WP; Metz, R; Muller, AJ; Prendergast, GC | 1 |
| Camara, CA; Costa, VA; da Silva Júnior, EN; de Araujo, AS; de Castro, SL; de Melo, IM; de Oliveira, RN; de Simone, CA; de Souza Filho, JD; Diogo, EB; dos Santos, MR; Emery, FS; Menna-Barreto, RF; Valença, WO | 1 |
4 other study(ies) available for lawsone and dichlone
| Article | Year |
|---|---|
Substituted 1,4-naphthoquinones vs. the ascitic sarcoma 180 of mice.
Topics: Animals; Lethal Dose 50; Magnetic Resonance Spectroscopy; Mathematics; Mice; Naphthoquinones; Sarcoma 180; Structure-Activity Relationship | 1983 |
The 1,4-naphthoquinone scaffold in the design of cysteine protease inhibitors.
Topics: Cathepsin B; Cysteine; Cysteine Proteinase Inhibitors; Models, Molecular; Molecular Structure; Naphthoquinones; Pancreatic Elastase; Papain | 2007 |
Indoleamine 2,3-dioxygenase is the anticancer target for a novel series of potent naphthoquinone-based inhibitors.
Topics: Animals; Antineoplastic Agents; Binding Sites; Cell Proliferation; Cell Survival; Computer Simulation; Crystallography, X-Ray; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Indoleamine-Pyrrole 2,3,-Dioxygenase; Mice; Mice, Knockout; Mice, Nude; Models, Molecular; Molecular Structure; Naphthoquinones; Pyrones; Stereoisomerism; Structure-Activity Relationship; Vitamin K 3 | 2008 |
On the search for potential anti-Trypanosoma cruzi drugs: synthesis and biological evaluation of 2-hydroxy-3-methylamino and 1,2,3-triazolic naphthoquinoidal compounds obtained by click chemistry reactions.
Topics: Animals; Chemistry Techniques, Synthetic; Click Chemistry; Drug Discovery; Mice; Naphthoquinones; Triazoles; Trypanocidal Agents; Trypanosoma cruzi | 2012 |