1.0 2010-04-08 22:04:38 UTC 2025-11-18 22:20:14 UTC FDB000602 Isoorientin 2''-glucoside Constituent of the leaves of melon (Cucumis melo) and rice (Oryza sativa). Isoorientin 2''-glucoside is found in many foods, some of which are rice, cereals and cereal products, muskmelon, and fruits. 3',4',5,7-Tetrahydroxy-6-C-sophorosylflavone Isoorientin 2''-glucoside Isoorientin 2''-O-glucopyranoside Meloside L C27H30O16 610.5175 610.153384912 6-[4,5-dihydroxy-6-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one 6-[4,5-dihydroxy-6-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 55196-48-0 OCC1OC(OC2C(O)C(O)C(CO)OC2C2=C(O)C3=C(OC(=CC3=O)C3=CC=C(O)C(O)=C3)C=C2O)C(O)C(O)C1O InChI=1S/C27H30O16/c28-6-15-20(35)23(38)26(43-27-24(39)22(37)19(34)16(7-29)42-27)25(41-15)18-12(33)5-14-17(21(18)36)11(32)4-13(40-14)8-1-2-9(30)10(31)3-8/h1-5,15-16,19-20,22-31,33-39H,6-7H2 QWAZWXOCSOFIPS-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 -0.61 ALOGPS logs -1.95 ALOGPS solubility 6.92e+00 g/l ALOGPS melting_point Mp 212° logp -2.1 ChemAxon pka_strongest_acidic 6.2 ChemAxon pka_strongest_basic -3.6 ChemAxon iupac 6-[4,5-dihydroxy-6-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one ChemAxon average_mass 610.5175 ChemAxon mono_mass 610.153384912 ChemAxon smiles OCC1OC(OC2C(O)C(O)C(CO)OC2C2=C(O)C3=C(OC(=CC3=O)C3=CC=C(O)C(O)=C3)C=C2O)C(O)C(O)C1O ChemAxon formula C27H30O16 ChemAxon inchi InChI=1S/C27H30O16/c28-6-15-20(35)23(38)26(43-27-24(39)22(37)19(34)16(7-29)42-27)25(41-15)18-12(33)5-14-17(21(18)36)11(32)4-13(40-14)8-1-2-9(30)10(31)3-8/h1-5,15-16,19-20,22-31,33-39H,6-7H2 ChemAxon inchikey QWAZWXOCSOFIPS-UHFFFAOYSA-N ChemAxon polar_surface_area 276.52 ChemAxon refractivity 140.43 ChemAxon polarizability 58.81 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 16 ChemAxon donor_count 11 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::NmrOneD 15602 Specdb::NmrOneD 15603 Specdb::NmrOneD 15604 Specdb::NmrOneD 15605 Specdb::NmrOneD 15606 Specdb::NmrOneD 15607 Specdb::NmrOneD 15608 Specdb::NmrOneD 15609 Specdb::NmrOneD 15610 Specdb::NmrOneD 15611 Specdb::NmrOneD 15612 Specdb::NmrOneD 15613 Specdb::NmrOneD 15614 Specdb::NmrOneD 15615 Specdb::NmrOneD 15616 Specdb::NmrOneD 15617 Specdb::NmrOneD 15618 Specdb::NmrOneD 15619 Specdb::NmrOneD 15620 Specdb::NmrOneD 15621 Specdb::CMs 13078 Specdb::CMs 41390 Specdb::CMs 501372 Specdb::CMs 501373 Specdb::CMs 501374 Specdb::CMs 501375 Specdb::CMs 501376 Specdb::CMs 501377 Specdb::CMs 501378 Specdb::CMs 501379 Specdb::CMs 501380 Specdb::CMs 501381 Specdb::CMs 501382 Specdb::CMs 501383 Specdb::CMs 501384 Specdb::CMs 501385 Specdb::CMs 501386 Specdb::CMs 501387 Specdb::CMs 501388 Specdb::CMs 501389 Specdb::CMs 501390 Specdb::CMs 501391 Specdb::CMs 501392 Specdb::CMs 501393 Specdb::CMs 501394 Specdb::MsMs 72921 Specdb::MsMs 72922 Specdb::MsMs 72923 Specdb::MsMs 131976 Specdb::MsMs 131977 Specdb::MsMs 131978 Specdb::MsMs 2254740 Specdb::MsMs 2255847 Specdb::MsMs 2733789 Specdb::MsMs 2733790 Specdb::MsMs 2733791 Specdb::MsMs 2971692 Specdb::MsMs 2971693 Specdb::MsMs 2971694 HMDB29478 #<Reference:0x000055ce30d71078> Breakfast cereal Type 2 specific Cereals and cereal products Unknown generic Fruits Unknown generic Muskmelon Type 1 specific Cucumis melo 3656 Rice Type 1 specific Oryza sativa 4530