EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C20H20O11 |
| Net Charge | 0 |
| Average Mass | 436.369 |
| Monoisotopic Mass | 436.10056 |
| SMILES | O=C1c2c(O)cc(O)cc2O[C@H](c2ccc(O)c(O)c2)[C@@H]1O[C@H]1OC[C@@H](O)[C@@H](O)[C@@H]1O |
| InChI | InChI=1S/C20H20O11/c21-8-4-11(24)14-13(5-8)30-18(7-1-2-9(22)10(23)3-7)19(16(14)27)31-20-17(28)15(26)12(25)6-29-20/h1-5,12,15,17-26,28H,6H2/t12-,15-,17+,18-,19-,20-/m1/s1 |
| InChIKey | UKSPRKDZNYSFRL-FIZZSBNSSA-N |
| Roles Classification |
|---|
| Biological Role: | metabolite Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| (−)-epitaxifolin 3-O-α-D-arabinopyranoside (CHEBI:75748) has functional parent (−)-epitaxifolin (CHEBI:75747) |
| (−)-epitaxifolin 3-O-α-D-arabinopyranoside (CHEBI:75748) has functional parent α-D-arabinopyranose (CHEBI:46995) |
| (−)-epitaxifolin 3-O-α-D-arabinopyranoside (CHEBI:75748) has role metabolite (CHEBI:25212) |
| (−)-epitaxifolin 3-O-α-D-arabinopyranoside (CHEBI:75748) is a 3'-hydroxyflavanones (CHEBI:48024) |
| (−)-epitaxifolin 3-O-α-D-arabinopyranoside (CHEBI:75748) is a 4'-hydroxyflavanones (CHEBI:140331) |
| (−)-epitaxifolin 3-O-α-D-arabinopyranoside (CHEBI:75748) is a flavanone glycoside (CHEBI:72730) |
| (−)-epitaxifolin 3-O-α-D-arabinopyranoside (CHEBI:75748) is a monosaccharide derivative (CHEBI:63367) |
| (−)-epitaxifolin 3-O-α-D-arabinopyranoside (CHEBI:75748) is a tetrahydroxyflavanone (CHEBI:38742) |
| (−)-epitaxifolin 3-O-α-D-arabinopyranoside (CHEBI:75748) is a α-D-arabinopyranoside (CHEBI:75745) |
| IUPAC Name |
|---|
| (2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-3,4-dihydro-2H-chromen-3-yl α-D-arabinopyranoside |
| Synonym | Source |
|---|---|
| (2R,3S)-epitaxifolin 3-O-α-D-arabinopyranoside | ChEBI |
| Registry Numbers | Sources |
|---|---|
| Reaxys:20407031 | Reaxys |