Effects of hydroxylation of flavonoids on affinities.
| Class | Ring | Position | Example | Affinity | Inhibition |
|---|---|---|---|---|---|
| Flavone | A | 5H→OH | 7-OH flavone → chrysin | ↓ | ↑ |
| 6H→OH | Chrysin → baicalein | ↑ | ↓ | ||
| 7H→OH | Flavone → 7-OH flavone | ↓ | ↑ | ||
| Baicalin → baicalein | ↓ | ↑ | |||
| B | 3′H→OH | Apigenin → luteolin | ↑ | ↑ | |
| 4′H→OH | Chrysin → apigenin | ↓ | ↑ | ||
| C | 3H→OH | Chrysin → galangin | ↑ | ↑ | |
| Apigenin → kaempferol | ↑ | ↓ | |||
| Luteolin → quercetin | ↓ | ↑ | |||
| Flavonol | A | 5H→OH | Fisetin → quercetin | ↓ | ↑ |
| B | 3′H→OH | Kaempferol → quercetin | ↑ | ↑ | |
| 4′H→OH | Galangin → kaempferol | ↑ | ↑ | ||
| 5′H→OH | Quercetin → myricetin | ↓ | ↓ | ||
| Isoflavone | A | 5H→OH | Daidzein → genistein | ↑ | ↓ |
| Formononetin → biochanin A | ↓ | ↓ | |||
| Flavanone | A | 7H→OH | Naringin → naringenin | ↓ | ↑ |