1.0 2010-04-08 22:14:58 UTC 2019-11-26 03:18:47 UTC FDB020343 Aloesol 7-glucoside Constituent of rhubarb Rheum species Aloesol 7-glucoside is found in green vegetables. Aloesol 7-glucoside Aloesol 7-O-b-D-glucopyranoside Aloesol 7-O-b-D-glucoside C19H24O9 396.3885 396.142032366 2-(2-hydroxypropyl)-5-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one 2-(2-hydroxypropyl)-5-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one 94356-36-2 CC(O)CC1=CC(=O)C2=C(O1)C=C(OC1OC(CO)C(O)C(O)C1O)C=C2C InChI=1S/C19H24O9/c1-8-3-10(27-19-18(25)17(24)16(23)14(7-20)28-19)6-13-15(8)12(22)5-11(26-13)4-9(2)21/h3,5-6,9,14,16-21,23-25H,4,7H2,1-2H3 OUFZAUOJAQUDOD-UHFFFAOYSA-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 Acetals Benzenoids Chromones Heteroaromatic compounds Hexoses Hydrocarbon derivatives O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Polyols Primary alcohols Pyranones and derivatives Secondary alcohols 1-benzopyran Acetal Alcohol Aromatic heteropolycyclic compound Benzenoid Benzopyran Chromone Heteroaromatic compound Hexose monosaccharide Hydrocarbon derivative Monosaccharide O-glycosyl compound Organic oxide Organoheterocyclic compound Oxacycle Oxane Phenolic glycoside Polyol Primary alcohol Pyran Pyranone Secondary alcohol logp -0.56 ALOGPS logs -2.21 ALOGPS solubility 2.44e+00 g/l ALOGPS melting_point Mp 191-193° logp -0.76 ChemAxon pka_strongest_acidic 12.2 ChemAxon pka_strongest_basic -2.6 ChemAxon iupac 2-(2-hydroxypropyl)-5-methyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one ChemAxon average_mass 396.3885 ChemAxon mono_mass 396.142032366 ChemAxon smiles CC(O)CC1=CC(=O)C2=C(O1)C=C(OC1OC(CO)C(O)C(O)C1O)C=C2C ChemAxon formula C19H24O9 ChemAxon inchi InChI=1S/C19H24O9/c1-8-3-10(27-19-18(25)17(24)16(23)14(7-20)28-19)6-13-15(8)12(22)5-11(26-13)4-9(2)21/h3,5-6,9,14,16-21,23-25H,4,7H2,1-2H3 ChemAxon inchikey OUFZAUOJAQUDOD-UHFFFAOYSA-N ChemAxon polar_surface_area 145.91 ChemAxon refractivity 97.1 ChemAxon polarizability 40.03 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 9 ChemAxon donor_count 5 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 25464 Specdb::CMs 46836 Specdb::CMs 136693 Specdb::CMs 144427 Specdb::MsMs 322414 Specdb::MsMs 322415 Specdb::MsMs 322416 Specdb::MsMs 370318 Specdb::MsMs 370319 Specdb::MsMs 370320 Specdb::MsMs 2272269 Specdb::MsMs 2272270 Specdb::MsMs 2272271 Specdb::MsMs 3069723 Specdb::MsMs 3069724 Specdb::MsMs 3069725 Specdb::NmrOneD 41982 Specdb::NmrOneD 41983 Specdb::NmrOneD 41984 Specdb::NmrOneD 41985 Specdb::NmrOneD 41986 Specdb::NmrOneD 41987 Specdb::NmrOneD 41988 Specdb::NmrOneD 41989 Specdb::NmrOneD 41990 Specdb::NmrOneD 41991 Specdb::NmrOneD 41992 Specdb::NmrOneD 41993 Specdb::NmrOneD 41994 Specdb::NmrOneD 41995 Specdb::NmrOneD 41996 Specdb::NmrOneD 41997 Specdb::NmrOneD 41998 Specdb::NmrOneD 41999 Specdb::NmrOneD 42000 Specdb::NmrOneD 42001 HMDB40565 #<Reference:0x000055ce31612880> Green vegetables Unknown generic