1.0 2010-04-08 22:13:37 UTC 2019-11-26 03:15:59 UTC FDB018301 D-Galactopyranosyl-(1->3)-D-galactopyranosyl-(1->3)-L-arabinose Isolated from the hydrolysate of the gum of Spondias dulcis (ambarella). D-Galactopyranosyl-(1->3)-D-galactopyranosyl-(1->3)-L-arabinose is found in fruits. C17H30O15 474.4111 474.15847029 2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-[(2,3,5-trihydroxyoxan-4-yl)oxy]oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-[(2,3,5-trihydroxyoxan-4-yl)oxy]oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 79043-15-5 OCC1OC(OC2C(O)C(CO)OC(OC3C(O)COC(O)C3O)C2O)C(O)C(O)C1O InChI=1S/C17H30O15/c18-1-5-7(21)9(23)10(24)16(29-5)32-14-8(22)6(2-19)30-17(12(14)26)31-13-4(20)3-28-15(27)11(13)25/h4-27H,1-3H2 USDVNAMKKXRXGK-UHFFFAOYSA-N belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. O-glycosyl compounds Organic compounds Organic oxygen compounds Organooxygen compounds Carbohydrates and carbohydrate conjugates Aliphatic heteromonocyclic compounds Acetals Disaccharides Hemiacetals Hydrocarbon derivatives Oxacyclic compounds Oxanes Polyols Primary alcohols Secondary alcohols Acetal Alcohol Aliphatic heteromonocyclic compound Disaccharide Hemiacetal Hydrocarbon derivative O-glycosyl compound Organoheterocyclic compound Oxacycle Oxane Polyol Primary alcohol Secondary alcohol logp -2.79 ALOGPS logs 0.11 ALOGPS solubility 6.09e+02 g/l ALOGPS logp -5.8 ChemAxon pka_strongest_acidic 11.22 ChemAxon pka_strongest_basic -3.5 ChemAxon iupac 2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-[(2,3,5-trihydroxyoxan-4-yl)oxy]oxan-4-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol ChemAxon average_mass 474.4111 ChemAxon mono_mass 474.15847029 ChemAxon smiles OCC1OC(OC2C(O)C(CO)OC(OC3C(O)COC(O)C3O)C2O)C(O)C(O)C1O ChemAxon formula C17H30O15 ChemAxon inchi InChI=1S/C17H30O15/c18-1-5-7(21)9(23)10(24)16(29-5)32-14-8(22)6(2-19)30-17(12(14)26)31-13-4(20)3-28-15(27)11(13)25/h4-27H,1-3H2 ChemAxon inchikey USDVNAMKKXRXGK-UHFFFAOYSA-N ChemAxon polar_surface_area 248.45 ChemAxon refractivity 94.79 ChemAxon polarizability 44.04 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 15 ChemAxon donor_count 10 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::NmrOneD 29722 Specdb::NmrOneD 29723 Specdb::NmrOneD 29724 Specdb::NmrOneD 29725 Specdb::NmrOneD 29726 Specdb::NmrOneD 29727 Specdb::NmrOneD 29728 Specdb::NmrOneD 29729 Specdb::NmrOneD 29730 Specdb::NmrOneD 29731 Specdb::NmrOneD 29732 Specdb::NmrOneD 29733 Specdb::NmrOneD 29734 Specdb::NmrOneD 29735 Specdb::NmrOneD 29736 Specdb::NmrOneD 29737 Specdb::NmrOneD 29738 Specdb::NmrOneD 29739 Specdb::NmrOneD 29740 Specdb::NmrOneD 29741 Specdb::MsMs 87795 Specdb::MsMs 87796 Specdb::MsMs 87797 Specdb::MsMs 150384 Specdb::MsMs 150385 Specdb::MsMs 150386 Specdb::MsMs 2800264 Specdb::MsMs 2800265 Specdb::MsMs 2800266 Specdb::MsMs 2878370 Specdb::MsMs 2878371 Specdb::MsMs 2878372 Specdb::CMs 19501 Specdb::CMs 46109 Specdb::CMs 134093 Specdb::CMs 141827 Specdb::CMs 160907 Specdb::CMs 160910 Specdb::CMs 160912 Specdb::CMs 160914 Specdb::CMs 160916 Specdb::CMs 160918 Specdb::CMs 160921 Specdb::CMs 160923 Specdb::CMs 160924 Specdb::CMs 160926 Specdb::CMs 160928 Specdb::CMs 160930 Specdb::CMs 160932 Specdb::CMs 160934 Specdb::CMs 160936 Specdb::CMs 160938 Specdb::CMs 280308 HMDB38862 #<Reference:0x000055ce315c7cb8> Fruits Unknown generic