General Characteristics
2D structure
NatID 75
Common Name 7-Hydroxyflavanone
Molecular Formula C15H12O3
Chemical Class Flavonoids > Flavans
Molecular Weight 240.079 g/mol
Other names (2S)-7-Hydroxyflavanone 7-hydroxyflavanone

 

Representations
Smiles O=C1C[C@@H](c2ccccc2)Oc2cc(O)ccc21
Inchi InChI=1S/C15H12O3/c16-11-6-7-12-13(17)9-14(18-15(12)8-11)10-4-2-1-3-5-10/h1-8,14,16H,9H2/t14-/m0/s1
Inchi Key SWAJPHCXKPCPQZ-AWEZNQCLSA-N
3D Structure

 

Calculated Properties
clogP 3.10
TPSA 46.53
HBD 1
HBA 3
Rotatable Bonds 1
Aromatic Rings 2
Heavy Atoms 18
Aromatic Carbocycles 2
Aromatic Heterocycles 0
Number of NO 3

 

Experiments
EID Source Semisynthetic? Confidence level References
9490 Zuccagnia punctata No Very High Pederiva, R., & Giordano, O. S. (1984). 37-Dihydroxy-8-methoxyflavone from Zuccagnia punctata. Phytochemistry, 23(6), 1340–1341. https://doi.org/10.1016/s0031-9422(00)80459-8 Svetaz, L., Tapia, A., López, S. N., Furlán, R. L. E., Petenatti, E., Pioli, R., Schmeda-Hirschmann, G., & Zacchino, S. A. (2004). Antifungal Chalcones and New Caffeic Acid Esters from Zuccagnia punctata Acting against Soybean Infecting Fungi. Journal of Agricultural and Food Chemistry, 52(11), 3297–3300. https://doi.org/10.1021/jf035213x
9932 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