1.0 2010-04-08 22:04:38 UTC 2025-11-18 22:20:20 UTC FDB000611 Isosakuranetin 7-glucoside Isolated from Prunus subspecies Isosakuranetin 7-glucoside is found in fruits. (2S)-Poncirenin (S)-5,7-Dihydroxy-4'-methoxyflavanone 7-O-b-D-glucopyranoside Isosakuranetin 7-glucoside Isosakuranetin 7-O-b-D-glucopyranoside Isosakuranetin 7-O-b-D-glucoside Isosakuranin Poncirenin C22H24O10 448.42 448.136946988 5-hydroxy-2-(4-methoxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-one 5-hydroxy-2-(4-methoxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzopyran-4-one 491-69-0 COC1=CC=C(C=C1)C1CC(=O)C2=C(O1)C=C(OC1OC(CO)C(O)C(O)C1O)C=C2O InChI=1S/C22H24O10/c1-29-11-4-2-10(3-5-11)15-8-14(25)18-13(24)6-12(7-16(18)31-15)30-22-21(28)20(27)19(26)17(9-23)32-22/h2-7,15,17,19-24,26-28H,8-9H2,1H3 KEEWIHDTSNESJZ-UHFFFAOYSA-N belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Flavonoid-7-O-glycosides Organic compounds Phenylpropanoids and polyketides Flavonoids Flavonoid glycosides Aromatic heteropolycyclic compounds 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids 4'-O-methylated flavonoids 5-hydroxyflavonoids Acetals Alkyl aryl ethers Anisoles Aryl alkyl ketones Chromones Flavanones Hexoses Hydrocarbon derivatives Methoxybenzenes O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Phenolic glycosides Phenoxy compounds Polyols Primary alcohols Secondary alcohols Vinylogous acids 1-benzopyran 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid 4p-methoxyflavonoid-skeleton 5-hydroxyflavonoid Acetal Alcohol Alkyl aryl ether Anisole Aromatic heteropolycyclic compound Aryl alkyl ketone Aryl ketone Benzenoid Benzopyran Chromane Chromone Ether Flavan Flavanone Flavonoid-7-o-glycoside Glycosyl compound Hexose monosaccharide Hydrocarbon derivative Hydroxyflavonoid Ketone Methoxybenzene Monocyclic benzene moiety Monosaccharide O-glycosyl compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Phenol ether Phenolic glycoside Phenoxy compound Polyol Primary alcohol Secondary alcohol Vinylogous acid logp 0.47 ALOGPS logs -2.64 ALOGPS solubility 1.02e+00 g/l ALOGPS melting_point Mp 214° (184-187°) logp 0.71 ChemAxon pka_strongest_acidic 9.84 ChemAxon pka_strongest_basic -3 ChemAxon iupac 5-hydroxy-2-(4-methoxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-one ChemAxon average_mass 448.42 ChemAxon mono_mass 448.136946988 ChemAxon smiles COC1=CC=C(C=C1)C1CC(=O)C2=C(O1)C=C(OC1OC(CO)C(O)C(O)C1O)C=C2O ChemAxon formula C22H24O10 ChemAxon inchi InChI=1S/C22H24O10/c1-29-11-4-2-10(3-5-11)15-8-14(25)18-13(24)6-12(7-16(18)31-15)30-22-21(28)20(27)19(26)17(9-23)32-22/h2-7,15,17,19-24,26-28H,8-9H2,1H3 ChemAxon inchikey KEEWIHDTSNESJZ-UHFFFAOYSA-N ChemAxon polar_surface_area 155.14 ChemAxon refractivity 107.92 ChemAxon polarizability 44.84 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 10 ChemAxon donor_count 5 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 10596 Specdb::CMs 41392 Specdb::CMs 167070 Specdb::MsMs 76260 Specdb::MsMs 76261 Specdb::MsMs 76262 Specdb::MsMs 136056 Specdb::MsMs 136057 Specdb::MsMs 136058 Specdb::MsMs 440339 Specdb::MsMs 440340 Specdb::MsMs 440341 Specdb::MsMs 440342 Specdb::MsMs 440343 Specdb::MsMs 440344 Specdb::MsMs 440345 Specdb::MsMs 440346 Specdb::MsMs 440347 Specdb::MsMs 440348 Specdb::MsMs 440349 Specdb::MsMs 440350 Specdb::MsMs 440351 Specdb::MsMs 440352 Specdb::MsMs 440353 Specdb::MsMs 440354 Specdb::MsMs 440355 Specdb::MsMs 440356 Specdb::MsMs 440357 HMDB0029481 Fruits Unknown generic