1.0 2012-01-13 17:26:27 UTC 2015-07-21 07:01:52 UTC FDB029920 Isopeonidin 3-arabinoside A polyphenol metabolite detected in biological fluids [PhenolExplorer] Isopeonidin 3-O-arabinoside C21H21O10 433.3854 433.113471892 3-{[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-1λ⁴-chromen-1-ylium 3-{[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-1λ⁴-chromen-1-ylium COC1=C(O)C=C(C=C1)C1=C(O[C@H]2O[C@H](CO)[C@@H](O)[C@@H]2O)C=C2C(O)=CC(O)=CC2=[O+]1 InChI=1S/C21H20O10/c1-28-14-3-2-9(4-13(14)25)20-16(30-21-19(27)18(26)17(8-22)31-21)7-11-12(24)5-10(23)6-15(11)29-20/h2-7,17-19,21-22,26-27H,8H2,1H3,(H2-,23,24,25)/p+1/t17-,18-,19+,21+/m1/s1 FXNWBJIHSLHFRS-BNDYYXHWSA-O belongs to the class of organic compounds known as anthocyanidin-3-o-glycosides. These are phenolic compounds containing one anthocyanidin moiety which is O-glycosidically linked to a carbohydrate moiety at the C3-position. Anthocyanidin-3-O-glycosides Organic compounds Phenylpropanoids and polyketides Flavonoids Flavonoid glycosides Aromatic heteropolycyclic compounds 1-benzopyrans 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids 3'-hydroxyflavonoids 4'-O-methylated flavonoids 5-hydroxyflavonoids 7-hydroxyflavonoids Acetals Alkyl aryl ethers Anisoles Anthocyanidins Flavonoid-3-O-glycosides Heteroaromatic compounds Hydrocarbon derivatives Methoxybenzenes Methoxyphenols O-glycosyl compounds Organic cations Oxacyclic compounds Pentoses Phenoxy compounds Primary alcohols Secondary alcohols Tetrahydrofurans 1-benzopyran 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid 3'-hydroxyflavonoid 4p-methoxyflavonoid-skeleton 5-hydroxyflavonoid 7-hydroxyflavonoid Acetal Alcohol Alkyl aryl ether Anisole Anthocyanidin Anthocyanidin-3-o-glycoside Aromatic heteropolycyclic compound Benzenoid Benzopyran Ether Flavonoid-3-o-glycoside Glycosyl compound Heteroaromatic compound Hydrocarbon derivative Hydroxyflavonoid Methoxybenzene Methoxyphenol Monocyclic benzene moiety Monosaccharide O-glycosyl compound Organic cation Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Pentose monosaccharide Phenol Phenol ether Phenoxy compound Primary alcohol Secondary alcohol Tetrahydrofuran logp 1.12 ALOGPS logs -3.18 ALOGPS solubility 3.08e-01 g/l ALOGPS logp 1.09 ChemAxon pka_strongest_acidic 6.4 ChemAxon pka_strongest_basic -3 ChemAxon iupac 3-{[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-1λ⁴-chromen-1-ylium ChemAxon average_mass 433.3854 ChemAxon mono_mass 433.113471892 ChemAxon smiles COC1=C(O)C=C(C=C1)C1=C(O[C@H]2O[C@H](CO)[C@@H](O)[C@@H]2O)C=C2C(O)=CC(O)=CC2=[O+]1 ChemAxon formula C21H21O10 ChemAxon inchi InChI=1S/C21H20O10/c1-28-14-3-2-9(4-13(14)25)20-16(30-21-19(27)18(26)17(8-22)31-21)7-11-12(24)5-10(23)6-15(11)29-20/h2-7,17-19,21-22,26-27H,8H2,1H3,(H2-,23,24,25)/p+1/t17-,18-,19+,21+/m1/s1 ChemAxon inchikey FXNWBJIHSLHFRS-BNDYYXHWSA-O ChemAxon polar_surface_area 162.21 ChemAxon refractivity 114.78 ChemAxon polarizability 42.22 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 9 ChemAxon donor_count 6 ChemAxon physiological_charge 0 ChemAxon formal_charge 1 ChemAxon Specdb::CMs 17533 Specdb::CMs 47527 Specdb::CMs 132929 Specdb::CMs 140663 Specdb::MsMs 304813 Specdb::MsMs 304814 Specdb::MsMs 304815 Specdb::MsMs 2453314 Specdb::MsMs 2453315 Specdb::MsMs 2453316 HMDB41750 #<Reference:0x000055ce30dc7ae0>