Características Generales
| NatID | 76 |
| Nombre Común | 7,4-Dihydroxy-3 -methoxyflavanone |
| Fórmula Molecular | C16H14O5 |
| Tipo Químico | Flavonoids > O-methylated flavonoids |
| Peso Molecular | 286.084 g/mol |
| Otros nombres |
Representaciones
| Smiles | COc1cc([C@@H]2CC(=O)c3ccc(O)cc3O2)ccc1O |
| Inchi | InChI=1S/C16H14O5/c1-20-16-6-9(2-5-12(16)18)14-8-13(19)11-4-3-10(17)7-15(11)21-14/h2-7,14,17-18H,8H2,1H3/t14-/m0/s1 |
| Inchi Key | VSYNGSXKXHXJHX-AWEZNQCLSA-N |
| Estructura 3D |
Propiedades calculadas
| clogP | 2.81 |
| TPSA | 75.99 |
| HBD | 2 |
| HBA | 5 |
| Enlaces Rotables | 2 |
| Anillos aromáticos | 2 |
| Átomos pesados | 21 |
| Carbociclos Aromáticos | 2 |
| Heterociclos Aromáticos | 0 |
| Número de NO | 5 |
Experimentos
| EID | Fuente | Semisintético? | Confidence level | Referencias |
|---|---|---|---|---|
| 9933 | Flourensia oolepis | No | High | Joray, M. B., Trucco, L. D., González, M. L., Napal, G. N. D., Palacios, S. M., Bocco, J. L., & Carpinella, M. C. (2015). Antibacterial and Cytotoxic Activity of Compounds Isolated fromFlourensia oolepis. Evidence-Based Complementary and Alternative Medicine, 2015, 1–11. https://doi.org/10.1155/2015/912484 |
| Bioassay ID | NPASS ID | Target | Activity type | Activity |
|---|---|---|---|---|
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