1.0 2016-09-30 23:23:57 UTC 2020-04-22 15:18:02 UTC BMDB0006599 BMDB06599 3-Galactosyllactose 3'-Galactosyllactose Galactosyl beta (1-3)-galactosyl beta (1-4)glucose Galactosyl alpha (1-3)-galactosyl beta (1-4)glucose Gal(beta1-3)-gal(beta1-4)GLC GAGGL Gal(alphal-3)-gal(betal-4)GLC C18H32O16 504.4371 504.169034976 (2R,3R,4R,5R)-4-{[(2S,3R,4S,5S,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,3,5,6-tetrahydroxyhexanal gaggl OC[C@@H](O)[C@@H](O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O)[C@H](O)[C@@H](O)C=O InChI=1S/C18H32O16/c19-1-5(23)9(25)15(6(24)2-20)33-18-14(30)16(11(27)8(4-22)32-18)34-17-13(29)12(28)10(26)7(3-21)31-17/h1,5-18,20-30H,2-4H2/t5-,6+,7+,8+,9+,10-,11-,12-,13+,14+,15+,16-,17-,18-/m0/s1 KZZUYHVLNLDKLB-KZCWKWOXSA-N belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. Organic compounds Organic oxygen compounds Organooxygen compounds Carbohydrates and carbohydrate conjugates Oligosaccharides Acetals Alkyl glycosides Alpha-hydroxyaldehydes Beta-hydroxy aldehydes Fatty alcohols Hydrocarbon derivatives O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Polyols Primary alcohols Secondary alcohols Acetal Alcohol Aldehyde Aliphatic heteromonocyclic compound Alkyl glycoside Alpha-hydroxyaldehyde Beta-hydroxy aldehyde Carbonyl group Fatty acyl Fatty acyl glycoside Fatty alcohol Glycosyl compound Hydrocarbon derivative O-glycosyl compound Oligosaccharide Organic oxide Organoheterocyclic compound Oxacycle Oxane Polyol Primary alcohol Secondary alcohol Aliphatic heteromonocyclic compounds Solid logp -2.84 ALOGPS logs -0.22 ALOGPS logp -7.1 ChemAxon pka_strongest_acidic 11.55 ChemAxon pka_strongest_basic -3.6 ChemAxon iupac (2R,3R,4R,5R)-4-{[(2S,3R,4S,5S,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,3,5,6-tetrahydroxyhexanal ChemAxon average_mass 504.4371 ChemAxon mono_mass 504.169034976 ChemAxon smiles OC[C@@H](O)[C@@H](O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)[C@H]1O)[C@H](O)[C@@H](O)C=O ChemAxon formula C18H32O16 ChemAxon inchi InChI=1S/C18H32O16/c19-1-5(23)9(25)15(6(24)2-20)33-18-14(30)16(11(27)8(4-22)32-18)34-17-13(29)12(28)10(26)7(3-21)31-17/h1,5-18,20-30H,2-4H2/t5-,6+,7+,8+,9+,10-,11-,12-,13+,14+,15+,16-,17-,18-/m0/s1 ChemAxon inchikey KZZUYHVLNLDKLB-KZCWKWOXSA-N ChemAxon polar_surface_area 276.52 ChemAxon refractivity 102.17 ChemAxon polarizability 46.27 ChemAxon rotatable_bond_count 11 ChemAxon acceptor_count 16 ChemAxon donor_count 11 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon number_of_rings 2 ChemAxon bioavailability 0 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::CMs 23959 Specdb::CMs 39053 Specdb::MsMs 319099 Specdb::MsMs 319100 Specdb::MsMs 319101 Specdb::MsMs 366088 Specdb::MsMs 366089 Specdb::MsMs 366090 189088 Deya, Eiki; Amaya, Mieko; Nojiri, Kaoru; Igarashi, Seiichio. Application of galactosyllactose for infant formula. I. Preparation of galactosyllactose by b-galactosidase. Yukijirushi Nyugyo Gijutsu Kenkyusho Hokoku (1982), (78), 19-26.