isoscopoletin has been researched along with esculetin in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (40.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
---|---|
Hecht, SM; Jones, SH; Ma, J | 1 |
Ferrari, AM; Gamberini, MC; Rastelli, G; Sgobba, M | 1 |
Adachi, I; Hirono, S; Kato, A; Kobayashi, K; Minoshima, Y; Narukawa, K; Nash, RJ | 1 |
Bari, SB; Deshmukh, PK; Donda, ST; Firke, SD; Patil, DA; Patil, PO | 1 |
Ge, GB; Gonzalez, FJ; Li, SY; Liu, Y; Wang, JJ; Wang, P; Xia, YL | 1 |
1 review(s) available for isoscopoletin and esculetin
Article | Year |
---|---|
A comprehensive review on synthesis and designing aspects of coumarin derivatives as monoamine oxidase inhibitors for depression and Alzheimer's disease.
Topics: Alzheimer Disease; Coumarins; Depression; Drug Design; Humans; Models, Molecular; Molecular Structure; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Structure-Activity Relationship | 2013 |
4 other study(ies) available for isoscopoletin and esculetin
Article | Year |
---|---|
A coumarin from Mallotus resinosus that mediates DNA cleavage.
Topics: Coumarins; DNA; DNA Damage; Mallotus Plant; Philippines; Plant Roots; Plants, Medicinal; Scopoletin | 2004 |
Relationship between quantum-chemical descriptors of proton dissociation and experimental acidity constants of various hydroxylated coumarins. Identification of the biologically active species for xanthine oxidase inhibition.
Topics: Coumarins; Hydrogen-Ion Concentration; Molecular Structure; Protons; Quantum Theory; Structure-Activity Relationship; Xanthine Oxidase | 2007 |
6,7-Dihydroxy-4-phenylcoumarin as inhibitor of aldose reductase 2.
Topics: Aldehyde Reductase; Animals; Binding Sites; Computer Simulation; Coumarins; Galactitol; L-Iditol 2-Dehydrogenase; Lens, Crystalline; Protein Structure, Tertiary; Rats; Rhodanine; Structure-Activity Relationship; Thiazolidines | 2010 |
Synthesis and structure-activity relationship of coumarins as potent Mcl-1 inhibitors for cancer treatment.
Topics: A549 Cells; Antineoplastic Agents; Cell Proliferation; Cell Survival; Coumarins; Dose-Response Relationship, Drug; Humans; Models, Molecular; Molecular Structure; Myeloid Cell Leukemia Sequence 1 Protein; Structure-Activity Relationship; Tumor Cells, Cultured | 2021 |