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flavanone glycoside
A member of the class of flavanones having one or more glycosyl residues attached at unspecified positions.
ChEBI ID: 72730
Members (10)
| Member | Definition | Role |
|---|---|---|
| astilbin | A flavanone glycoside that is (+)-taxifolin substituted by a alpha-L-rhamnosyl moiety at position 3 via a glycosidic linkage. | astilbin |
| butrin | A flavanone glycoside that is butin substituted by two beta-D-glucopyranosyl residues at positions 7 and 3' respectively. | butrin |
| eriocitrin | A disaccharide derivative that consists of eriodictyol substituted by a 6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. | eriocitrin |
| eriodictyol 7-O-beta-D-glucopyranoside | A flavanone glycoside that is eriodictyol attached to a beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage. It is an Nrf2 activator and provides protection against cisplatin-induced toxicity. | eriodictyol 7-O-beta-D-glucopyranoside |
| hesperidin | A disaccharide derivative that consists of hesperetin substituted by a 6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. | hesperidin |
| likviriton | A flavanone glycoside that is liquiritigenin attached to a beta-D-glucopyranosyl residue at position 4' via a glycosidic linkage. | liquiritin |
| methyl hesperidin | A flavanone glycoside that is hesperidin in which the hydroxy group at position 3' has been replaced by a methoxy group. | methyl hesperidin |
| neoastilbin | A flavanone glycoside that is (-)-taxifolin substituted by a alpha-L-rhamnosyl moiety at position 3 via a glycosidic linkage. | neoastilbin |
| neoeriocitrin | A flavanone glycoside that is eriodictyol substituted by a 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl residue at position 7 via a glycosidic linkage. | neoeriocitrin |
| phellamurin | A member of the class of dihydroflavonols that is (+)-dihydrokaempferol substituted by a prenyl group at position 8 and a beta-D-glucopyranosyl group at position 7 via a glycosidic linkage. Isolated from Phellodendron amurense and Commiphora africana, it exhibits inhibition of intestinal P-glycoprotein. | phellamurin |
Research
Studies (2,167)
| Timeframe | Studies, Drugs in This Class (%) | All Drugs % |
|---|---|---|
| pre-1990 | 135 (6.23) | 18.7374 |
| 1990's | 111 (5.12) | 18.2507 |
| 2000's | 349 (16.11) | 29.6817 |
| 2010's | 1,023 (47.21) | 24.3611 |
| 2020's | 549 (25.33) | 2.80 |
Study Types
| Publication Type | Studies, Drugs in This Class (%) | All Drugs (%) |
|---|---|---|
| Trials | 121 (5.25%) | 5.53% |
| Reviews | 90 (3.91%) | 6.00% |
| Case Studies | 7 (0.30%) | 4.05% |
| Observational | 7 (0.30%) | 0.25% |
| Other | 2,079 (90.23%) | 84.16% |