Abstract
The paper briefly summarizes methods to determine the structure of β-diketones with emphasis on NMR methods. Density functional calculations are also briefly treated. Emphasis is on the tautomeric equilibria of β-diketones in relation to biological effects. Relevant physical parameters such as acidity and solubility are treated. A series of biologically active molecules are treated with respect to structure (tautomerism). Characteristic molecules or groups of molecules are usnic acids, tetramic and tetronic acids, o-hydroxydibenzoylmethanes, curcumines, lupulones, and hyperforines.
| Original language | English |
|---|---|
| Article number | 1189 |
| Journal | Pharmaceuticals |
| Volume | 14 |
| Issue number | 11 |
| ISSN | 1424-8247 |
| DOIs | |
| Publication status | Published - Nov 2021 |
Bibliographical note
This article belongs to the Special Issue β-Diketones and Their Derivatives: Synthesis, Characterization and Biomedical ApplicationsUN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- biological effects
- DFT calculations
- tautomerism
- SAR
Citation Styles
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver