1.0 2026-09-21 16:23:58 UTC 2026-09-21 16:23:58 UTC FDB116726 Kanosamine (2R,3S,4S,5R)-3-amino-2,4,5,6-tetrahydroxy-hexanal (2R,3S,4S,5R)-3-amino-2,4,5,6-tetrahydroxyhexanal C6H13NO5 179.172 179.079372523 (2R,3S,4S,5R)-3-amino-2,4,5,6-tetrahydroxyhexanal kanosamine [H][C@@](O)(CO)[C@@]([H])(O)[C@]([H])(N)[C@@]([H])(O)C=O InChI=1S/C6H13NO5/c7-5(3(10)1-8)6(12)4(11)2-9/h1,3-6,9-12H,2,7H2/t3-,4+,5+,6+/m0/s1 FOEXHEVNPRRHDY-SLPGGIOYSA-N belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity. Hexoses Organic compounds Organic oxygen compounds Organooxygen compounds Carbohydrates and carbohydrate conjugates Aliphatic acyclic compounds 1,2-aminoalcohols 1,3-aminoalcohols Alpha-hydroxyaldehydes Hydrocarbon derivatives Monoalkylamines Organic oxides Organopnictogen compounds Polyols Primary alcohols Secondary alcohols 1,2-aminoalcohol 1,3-aminoalcohol Alcohol Aldehyde Aliphatic acyclic compound Alpha-hydroxyaldehyde Amine Carbonyl group Hexose monosaccharide Hydrocarbon derivative Organic nitrogen compound Organic oxide Organonitrogen compound Organopnictogen compound Polyol Primary alcohol Primary aliphatic amine Primary amine Secondary alcohol D-kanosamine logp -2.67 ALOGPS logs 0.05 ALOGPS solubility 1.99e+02 g/l ALOGPS logp -3.7 ChemAxon pka_strongest_acidic 12.69 ChemAxon pka_strongest_basic 8.11 ChemAxon iupac (2R,3S,4S,5R)-3-amino-2,4,5,6-tetrahydroxyhexanal ChemAxon average_mass 179.172 ChemAxon mono_mass 179.079372523 ChemAxon smiles [H][C@@](O)(CO)[C@@]([H])(O)[C@]([H])(N)[C@@]([H])(O)C=O ChemAxon formula C6H13NO5 ChemAxon inchi InChI=1S/C6H13NO5/c7-5(3(10)1-8)6(12)4(11)2-9/h1,3-6,9-12H,2,7H2/t3-,4+,5+,6+/m0/s1 ChemAxon inchikey FOEXHEVNPRRHDY-SLPGGIOYSA-N ChemAxon polar_surface_area 124.01 ChemAxon refractivity 39 ChemAxon polarizability 16.61 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 6 ChemAxon donor_count 5 ChemAxon physiological_charge 1 ChemAxon formal_charge 0 ChemAxon