1.0 2019-10-15 23:07:11 UTC 2019-10-15 23:07:11 UTC FDB093693 Enterodiol glucuronide C24H30O10 478.494 478.183897166 (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{3-[(2R,3R)-4-hydroxy-2-(hydroxymethyl)-3-[(3-hydroxyphenyl)methyl]butyl]phenoxy}oxane-2-carboxylic acid (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{3-[(2R,3R)-4-hydroxy-2-(hydroxymethyl)-3-[(3-hydroxyphenyl)methyl]butyl]phenoxy}oxane-2-carboxylic acid [H][C@@](CO)(CC1=CC(O)=CC=C1)[C@]([H])(CO)CC1=CC(O[C@]2([H])O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(O)[C@@]2([H])O)=CC=C1 InChI=1S/C24H30O10/c25-11-15(7-13-3-1-5-17(27)9-13)16(12-26)8-14-4-2-6-18(10-14)33-24-21(30)19(28)20(29)22(34-24)23(31)32/h1-6,9-10,15-16,19-22,24-30H,7-8,11-12H2,(H,31,32)/t15-,16-,19-,20-,21+,22-,24+/m0/s1 AHSOMLRDSRNEEA-NXZKRJRCSA-N belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones. Lignan glycosides Organic compounds Lignans, neolignans and related compounds Lignan glycosides Aromatic heteromonocyclic compounds 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Acetals Beta hydroxy acids and derivatives Carbonyl compounds Carboxylic acids Dibenzylbutanediol lignans Hydrocarbon derivatives Monocarboxylic acids and derivatives Monosaccharides O-glucuronides O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Phenol ethers Phenolic glycosides Phenoxy compounds Polyols Primary alcohols Pyrans Secondary alcohols 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid 1-o-glucuronide Acetal Alcohol Aromatic heteromonocyclic compound Benzenoid Beta-hydroxy acid Carbonyl group Carboxylic acid Carboxylic acid derivative Dibenzylbutane lignan skeleton Dibenzylbutanediol Glucuronic acid or derivatives Glycosyl compound Hydrocarbon derivative Hydroxy acid Lignan glycoside Monocarboxylic acid or derivatives Monocyclic benzene moiety Monosaccharide O-glucuronide O-glycosyl compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Phenol Phenol ether Phenolic glycoside Phenoxy compound Polyol Primary alcohol Pyran Secondary alcohol logp 0.89 ALOGPS logs -2.99 ALOGPS solubility 4.85e-01 g/l ALOGPS logp 0.7 ChemAxon pka_strongest_acidic 3.37 ChemAxon pka_strongest_basic -2.6 ChemAxon iupac (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{3-[(2R,3R)-4-hydroxy-2-(hydroxymethyl)-3-[(3-hydroxyphenyl)methyl]butyl]phenoxy}oxane-2-carboxylic acid ChemAxon average_mass 478.494 ChemAxon mono_mass 478.183897166 ChemAxon smiles [H][C@@](CO)(CC1=CC(O)=CC=C1)[C@]([H])(CO)CC1=CC(O[C@]2([H])O[C@]([H])(C(O)=O)[C@@]([H])(O)[C@]([H])(O)[C@@]2([H])O)=CC=C1 ChemAxon formula C24H30O10 ChemAxon inchi InChI=1S/C24H30O10/c25-11-15(7-13-3-1-5-17(27)9-13)16(12-26)8-14-4-2-6-18(10-14)33-24-21(30)19(28)20(29)22(34-24)23(31)32/h1-6,9-10,15-16,19-22,24-30H,7-8,11-12H2,(H,31,32)/t15-,16-,19-,20-,21+,22-,24+/m0/s1 ChemAxon inchikey AHSOMLRDSRNEEA-NXZKRJRCSA-N ChemAxon polar_surface_area 177.14 ChemAxon refractivity 118.37 ChemAxon polarizability 47.97 ChemAxon rotatable_bond_count 10 ChemAxon acceptor_count 10 ChemAxon donor_count 7 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 137515 Specdb::CMs 145249 Specdb::MsMs 2375423 Specdb::MsMs 2375424 Specdb::MsMs 2375425 Specdb::MsMs 2559402 Specdb::MsMs 2559403 Specdb::MsMs 2559404 FOBI:030616