1.0 2010-04-08 22:11:59 UTC 2018-05-29 01:20:55 UTC FDB015680 Eucaglobulin Constituent of Eucalyptus globulus (Tasmanian blue gum) Eucaglobulin C23H30O12 498.4771 498.173726424 3,4,5-trihydroxy-6-{[4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carbonyloxy]methyl}oxan-2-yl 3,4,5-trihydroxybenzoate 3,4,5-trihydroxy-6-{[4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carbonyloxy]methyl}oxan-2-yl 3,4,5-trihydroxybenzoate 241130-84-7 CC(C)(O)C1CCC(=CC1)C(=O)OCC1OC(OC(=O)C2=CC(O)=C(O)C(O)=C2)C(O)C(O)C1O InChI=1S/C23H30O12/c1-23(2,32)12-5-3-10(4-6-12)20(30)33-9-15-17(27)18(28)19(29)22(34-15)35-21(31)11-7-13(24)16(26)14(25)8-11/h3,7-8,12,15,17-19,22,24-29,32H,4-6,9H2,1-2H3 GMBUWWLCKJYTTG-UHFFFAOYSA-N belongs to the class of organic compounds known as saccharolipids. Saccharolipids are compounds in which fatty acids are linked directly to a sugar backbone, forming structures that are compatible with membrane bilayers. In the saccharolipids, a sugar substitutes for the glycerol backbone that is present in glycerolipids and glycerophospholipids. The most familiar saccharolipids contain an acylated glucosamine. In contrast to others glycolipids, the fatty acid is not glycosidically linked to the sugar moiety. Saccharolipids Organic compounds Lipids and lipid-like molecules Saccharolipids Aromatic heteromonocyclic compounds 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Acetals Aromatic monoterpenoids Benzoyl derivatives Carbonyl compounds Dicarboxylic acids and derivatives Enoate esters Galloyl esters Hydrocarbon derivatives Menthane monoterpenoids Monocyclic monoterpenoids Monosaccharides Organic oxides Oxacyclic compounds Oxanes Polyols Pyrogallols and derivatives Secondary alcohols Tannins Tertiary alcohols m-Hydroxybenzoic acid esters p-Hydroxybenzoic acid alkyl esters 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid Acetal Alcohol Alpha,beta-unsaturated carboxylic ester Aromatic heteromonocyclic compound Aromatic monoterpenoid Benzenetriol Benzenoid Benzoate ester Benzoic acid or derivatives Benzoyl Carbonyl group Carboxylic acid derivative Carboxylic acid ester Dicarboxylic acid or derivatives Enoate ester Gallic acid or derivatives Galloyl ester Hydrocarbon derivative M-hydroxybenzoic acid ester Monocyclic benzene moiety Monocyclic monoterpenoid Monosaccharide Monoterpenoid Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane P-hydroxybenzoic acid alkyl ester P-hydroxybenzoic acid ester P-menthane monoterpenoid Phenol Polyol Pyrogallol derivative Saccharolipid Secondary alcohol Tannin Tertiary alcohol logp 1.14 ALOGPS logs -2.42 ALOGPS solubility 1.88e+00 g/l ALOGPS logp 0.92 ChemAxon pka_strongest_acidic 8.08 ChemAxon pka_strongest_basic -0.87 ChemAxon iupac 3,4,5-trihydroxy-6-{[4-(2-hydroxypropan-2-yl)cyclohex-1-ene-1-carbonyloxy]methyl}oxan-2-yl 3,4,5-trihydroxybenzoate ChemAxon average_mass 498.4771 ChemAxon mono_mass 498.173726424 ChemAxon smiles CC(C)(O)C1CCC(=CC1)C(=O)OCC1OC(OC(=O)C2=CC(O)=C(O)C(O)=C2)C(O)C(O)C1O ChemAxon formula C23H30O12 ChemAxon inchi InChI=1S/C23H30O12/c1-23(2,32)12-5-3-10(4-6-12)20(30)33-9-15-17(27)18(28)19(29)22(34-15)35-21(31)11-7-13(24)16(26)14(25)8-11/h3,7-8,12,15,17-19,22,24-29,32H,4-6,9H2,1-2H3 ChemAxon inchikey GMBUWWLCKJYTTG-UHFFFAOYSA-N ChemAxon polar_surface_area 203.44 ChemAxon refractivity 118.38 ChemAxon polarizability 49.12 ChemAxon rotatable_bond_count 8 ChemAxon acceptor_count 10 ChemAxon donor_count 7 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 21656 Specdb::CMs 45009 Specdb::CMs 151705 Specdb::MsMs 80922 Specdb::MsMs 80923 Specdb::MsMs 80924 Specdb::MsMs 141909 Specdb::MsMs 141910 Specdb::MsMs 141911 Specdb::MsMs 2722059 Specdb::MsMs 2722060 Specdb::MsMs 2722061 Specdb::MsMs 2959434 Specdb::MsMs 2959435 Specdb::MsMs 2959436 HMDB36742 #<Reference:0x000055ce32352dd8>