1.0 2010-04-08 22:06:19 UTC 2025-11-18 22:56:52 UTC FDB004603 Rutinose Rutinose, also known as 6-O-(6-deoxy-alpha-L-mannopyranosyl)-D-glucose or (α-rhamnopyranosyl-β-glucopyranose, is a member of the class of compounds known as O-glycosyl compounds. O-glycosyl compounds are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Rutinose is soluble (in water) and a very weakly acidic compound (based on its pKa). Rutinose can be found in capers, which makes rutinose a potential biomarker for the consumption of this food product. Rutinose C12H22O10 326.2971 326.121296924 (2R,3R,4S,5S,6R)-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxane-2,3,4,5-tetrol rutinose 90-74-4 C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O InChI=1S/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12+/m0/s1 OVVGHDNPYGTYIT-BNXXONSGSA-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 Secondary alcohols Acetal Alcohol Aliphatic heteromonocyclic compound Disaccharide Hemiacetal Hydrocarbon derivative O-glycosyl compound Organoheterocyclic compound Oxacycle Oxane Polyol Secondary alcohol Disaccharides glycosylglucose logp -2.44 ALOGPS logs 0.10 ALOGPS solubility 4.07e+02 g/l ALOGPS melting_point 190.5 oC logp -3.7 ChemAxon pka_strongest_acidic 11.25 ChemAxon pka_strongest_basic -3.6 ChemAxon iupac (2R,3R,4S,5S,6R)-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxane-2,3,4,5-tetrol ChemAxon average_mass 326.2971 ChemAxon mono_mass 326.121296924 ChemAxon smiles C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O ChemAxon formula C12H22O10 ChemAxon inchi InChI=1S/C12H22O10/c1-3-5(13)7(15)10(18)12(21-3)20-2-4-6(14)8(16)9(17)11(19)22-4/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12+/m0/s1 ChemAxon inchikey OVVGHDNPYGTYIT-BNXXONSGSA-N ChemAxon polar_surface_area 169.3 ChemAxon refractivity 66.79 ChemAxon polarizability 30.17 ChemAxon rotatable_bond_count 3 ChemAxon acceptor_count 10 ChemAxon donor_count 7 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 53406 Specdb::MsMs 53407 Specdb::MsMs 53408 Specdb::MsMs 168816 Specdb::MsMs 168817 Specdb::MsMs 168818 Specdb::MsMs 3600674 Specdb::MsMs 3600675 Specdb::MsMs 3600676 Specdb::MsMs 3600677 Specdb::MsMs 3600678 Specdb::MsMs 3600679 27522 Apricot Type 1 specific Prunus armeniaca 36596 Asparagus Type 1 specific Asparagus officinalis 4686 Black tea Type 1 Blackberry Type 1 specific Rubus Capers Type 1 specific Capparis spinosa 65558 Cherry tomato Type 1 specific Solanum lycopersicum var. cerasiforme 195583 Fruit juice Type 2 specific Green tea Type 1 Olive Type 1 specific Olea europaea 4146 Sweet cherry Type 1 specific Prunus avium 42229