levobunolol has been researched along with cortistatin a in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, DY; Lim, CS; Nicolaou, KC; Peng, XS; Polet, D; Sun, YP; Zou, B | 1 |
| Chiu, P; Liu, LL | 1 |
| Himuro, M; Hirama, M; Iso, K; Kitajima, K; Yamashita, S | 1 |
| Chiu, P; Kuang, L; Liu, LL | 1 |
4 other study(ies) available for levobunolol and cortistatin a
| Article | Year |
|---|---|
Total synthesis and biological evaluation of cortistatins A and J and analogues thereof.
Topics: Biological Products; Cell Line, Tumor; Cell Proliferation; Heterocyclic Compounds, 4 or More Rings; Humans; Inhibitory Concentration 50; Isoquinolines; Polycyclic Compounds | 2009 |
An expeditious asymmetric synthesis of the pentacyclic core of the cortistatins by an intramolecular (4+3) cycloaddition.
Topics: Heterocyclic Compounds, 4 or More Rings; Isoquinolines; Polycyclic Compounds; Stereoisomerism; Substrate Specificity | 2011 |
Total synthesis of cortistatins A and J.
Topics: Alkaloids; Angiogenesis Inhibitors; Animals; Aquatic Organisms; Cyclization; Heterocyclic Compounds, 4 or More Rings; Isoquinolines; Ketones; Neovascularization, Pathologic; Neovascularization, Physiologic; Neuropeptides; Polycyclic Compounds; Porifera; Stereoisomerism; Steroids | 2011 |
Formal total synthesis of (+)-cortistatins A and J.
Topics: Cycloaddition Reaction; Epoxy Compounds; Heterocyclic Compounds, 4 or More Rings; Isoquinolines; Molecular Structure; Polycyclic Compounds; Silanes; Stereoisomerism | 2015 |