1.0 2020-04-02 17:44:14 UTC 2025-11-19 03:07:45 UTC FDB097274 Eriodictyol-6-C-glucoside C21H22O11 450.396 450.116211528 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-1-benzopyran-4-one 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydro-1-benzopyran-4-one OC[C@@H]1O[C@H]([C@H](O)[C@H](O)[C@@H]1O)C1=C(O)C=C2O[C@H](CC(=O)C2=C1O)C1=CC(O)=C(O)C=C1 InChI=1S/C21H22O11/c22-6-14-17(27)19(29)20(30)21(32-14)16-11(26)5-13-15(18(16)28)10(25)4-12(31-13)7-1-2-8(23)9(24)3-7/h1-3,5,12,14,17,19-24,26-30H,4,6H2/t12-,14+,17-,19-,20-,21+/m1/s1 FNJRUYGFVNGXTL-NLONATAVSA-N belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Phenolic glycosides Organic compounds Organic oxygen compounds Organooxygen compounds Carbohydrates and carbohydrate conjugates Aromatic heteropolycyclic compounds 1-hydroxy-2-unsubstituted benzenoids Acetals Amino acids Aralkylamines Azacyclic compounds Carbonyl compounds Carboxylic acids Enamines Heteroaromatic compounds Hexoses Hydrocarbon derivatives Indolecarboxylic acids L-alpha-amino acids O-glycosyl compounds Organic oxides Organopnictogen compounds Oxacyclic compounds Oxanes Polyols Primary alcohols Pyridinecarboxylic acids Secondary alcohols Tertiary alkylarylamines Tricarboxylic acids and derivatives 1-hydroxy-2-unsubstituted benzenoid Acetal Alcohol Alpha-amino acid Alpha-amino acid or derivatives Amine Amino acid Amino acid or derivatives Aralkylamine Aromatic heteropolycyclic compound Azacycle Benzenoid Carbonyl group Carboxylic acid Carboxylic acid derivative Enamine Heteroaromatic compound Hexose monosaccharide Hydrocarbon derivative Indole or derivatives Indolecarboxylic acid Indolecarboxylic acid derivative L-alpha-amino acid Monosaccharide O-glycosyl compound Organic nitrogen compound Organic oxide Organoheterocyclic compound Organonitrogen compound Organopnictogen compound Oxacycle Oxane Phenolic glycoside Polyol Primary alcohol Pyridine Pyridine carboxylic acid Pyridine carboxylic acid or derivatives Secondary alcohol Tertiary aliphatic/aromatic amine Tertiary amine Tricarboxylic acid or derivatives logp -0.10 ALOGPS logs -2.15 ALOGPS solubility 3.18e+00 g/l ALOGPS logp -0.23 ChemAxon pka_strongest_acidic 7.42 ChemAxon pka_strongest_basic -3.6 ChemAxon iupac 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-1-benzopyran-4-one ChemAxon average_mass 450.396 ChemAxon mono_mass 450.116211528 ChemAxon smiles OC[C@@H]1O[C@H]([C@H](O)[C@H](O)[C@@H]1O)C1=C(O)C=C2O[C@H](CC(=O)C2=C1O)C1=CC(O)=C(O)C=C1 ChemAxon formula C21H22O11 ChemAxon inchi InChI=1S/C21H22O11/c22-6-14-17(27)19(29)20(30)21(32-14)16-11(26)5-13-15(18(16)28)10(25)4-12(31-13)7-1-2-8(23)9(24)3-7/h1-3,5,12,14,17,19-24,26-30H,4,6H2/t12-,14+,17-,19-,20-,21+/m1/s1 ChemAxon inchikey FNJRUYGFVNGXTL-NLONATAVSA-N ChemAxon polar_surface_area 197.37 ChemAxon refractivity 106.39 ChemAxon polarizability 44.12 ChemAxon rotatable_bond_count 3 ChemAxon acceptor_count 11 ChemAxon donor_count 8 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 239749 Specdb::MsMs 239750 Specdb::MsMs 239751 Specdb::MsMs 241804 Specdb::MsMs 241805 Specdb::MsMs 241806 Milk (Cow) Type 2 specific 38.495 117.0 0.58 uM