mansonone f has been researched along with sesquiterpenes in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 5 (83.33) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cui, Z; Ikejima, T; Onodera, S; Tashiro, S; Wang, D; Xia, M | 1 |
Chae, JH; Choi, NS; Hyun, SS; Jeong, JM; Kim, SH; Kim, SN; Lee, KO; Lee, YS; Seo, SY; Shin, DY; Suh, YG | 1 |
Choi, EC; Choi, SH; Han, SM; Hyun, SS; Kim, SN; Lee, DS; Li, F; Min, KH; Shin, DY; Suh, YG | 1 |
Banerjee, AK; Ng, PS | 1 |
Gu, LQ; Huang, SL; Huang, ZS; Lee, KS; Li, MM; Liu, Z | 1 |
Chen, SB; Gu, LQ; Huang, SL; Huang, ZH; Huang, ZS; Li, D; Ou, JB; Ou, TM; Shen, LL; Tan, JH; Wu, WB | 1 |
6 other study(ies) available for mansonone f and sesquiterpenes
Article | Year |
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Cytotoxic effects of mansonone E and F isolated from Ulmus pumila.
Topics: Adult; Antineoplastic Agents, Phytogenic; Cell Line, Tumor; Cells, Cultured; Dose-Response Relationship, Drug; Growth Inhibitors; HeLa Cells; Humans; Leukocytes, Mononuclear; Naphthoquinones; Plant Extracts; Plant Roots; Sesquiterpenes; Ulmus | 2004 |
Syntheses and anti-MRSA activities of the C3 analogs of mansonone F, a potent anti-bacterial sesquiterpenoid: insights into its structural requirements for anti-MRSA activity.
Topics: Anti-Bacterial Agents; Humans; Methicillin Resistance; Microbial Sensitivity Tests; Naphthoquinones; Sesquiterpenes; Staphylococcus aureus; Structure-Activity Relationship | 2004 |
The structure-activity relationships of mansonone F, a potent anti-MRSA sesquiterpenoid quinone: SAR studies on the C6 and C9 analogs.
Topics: Anti-Infective Agents; Drug Resistance, Bacterial; Methicillin; Models, Chemical; Naphthoquinones; Quinones; Sesquiterpenes; Staphylococcal Infections; Staphylococcus aureus; Structure-Activity Relationship; Vancomycin | 2006 |
Alternative procedure for the synthesis of Mansonone F and Biflorin precursor.
Topics: Ketones; Magnetic Resonance Spectroscopy; Mass Spectrometry; Naphthols; Naphthoquinones; Pyrans; Sesquiterpenes; Spectrophotometry, Infrared; Tetralones | 2006 |
Inhibition of thioredoxin reductase by mansonone F analogues: Implications for anticancer activity.
Topics: Antineoplastic Agents; Apoptosis; Cell Cycle; Cell Proliferation; Cytochromes c; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Flow Cytometry; HeLa Cells; Humans; Intracellular Space; Kinetics; NADPH Oxidases; Naphthoquinones; Necrosis; Reactive Oxygen Species; Sesquiterpenes; Superoxides; Thioredoxin-Disulfide Reductase | 2009 |
Synthesis and evaluation of mansonone F derivatives as topoisomerase inhibitors.
Topics: Adenocarcinoma; Adenocarcinoma of Lung; Antigens, Neoplasm; Antineoplastic Agents; Carcinoma; Cell Line, Tumor; Cell Survival; DNA; DNA Topoisomerases, Type I; DNA Topoisomerases, Type II; DNA-Binding Proteins; Drug Screening Assays, Antitumor; Etoposide; Humans; Inhibitory Concentration 50; Lung Neoplasms; Naphthoquinones; Nasopharyngeal Carcinoma; Nasopharyngeal Neoplasms; Plasmids; Pyrans; Quinones; Sesquiterpenes; Structure-Activity Relationship; Telomerase; Topoisomerase Inhibitors | 2011 |