<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4402</id>
  <title>T3D4348</title>
  <common-name>D-Galactose</common-name>
  <description>D-Galactose is an aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. D-Galactose is an energy-providing nutrient and also a necessary basic substrate for the biosynthesis of many macromolecules in the body. Metabolic pathways for D-Galactose are important not only for the provision of these pathways but also for the prevention of D-Galactose and D-Galactose metabolite accumulation. The main source of D-Galactose is lactose in the milk of mammals, but it can also be found in some fruits and vegetables. Utilization of D-Galactose in all living cells is initiated by the phosphorylation of the hexose by the enzyme galactokinase (E.C. 2.7.1.6) (GALK) to form D-Galactose-1-phosphate. In the presence of D-Galactose-1-phosphate uridyltransferase (E.C. 2.7.7.12) (GALT) D-Galactose-1-phosphate is exchanged with glucose-1-phosphate in UDP-glucose to form UDP-galactose. Glucose-1-phosphate will then enter the glycolytic pathway for energy production. Deficiency of the enzyme GALT in galactosemic patients leads to the accumulation of D-Galactose-1-phosphate. Classic galactosemia-a term that denotes the presence of D-Galactose in the blood is the rare inborn error of D-Galactose metabolism, diagnosed by the deficiency of the second enzyme of the D-Galactose assimilation pathway, GALT, which, in turn, is caused by mutations at the GALT gene.  (A3437, A3438, A3439).</description>
  <cas>59-23-4</cas>
  <pubchem-id>439357</pubchem-id>
  <chemical-formula>C6H12O6</chemical-formula>
  <weight>180.16</weight>
  <appearance>White powder.</appearance>
  <melting-point>170°C</melting-point>
  <boiling-point></boiling-point>
  <density nil="true"/>
  <solubility>683.0 mg/mL</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure nil="true"/>
  <target nil="true"/>
  <mechanism-of-toxicity nil="true"/>
  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>This is an endogenously produced metabolite found in the human body. It is used in metabolic reactions, catabolic reactions or waste generation.</use-source>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2014-08-29T06:31:09Z</created-at>
  <updated-at type="dateTime">2026-05-14T19:12:16Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Hexose</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C00984</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>28061</chebi-id>
  <biocyc-id>GALACTOSE</biocyc-id>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB11735</drugbank-id>
  <pdb-id>GLA</pdb-id>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O</moldb-smiles>
  <moldb-formula>C6H12O6</moldb-formula>
  <moldb-inchi>InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6+/m1/s1</moldb-inchi>
  <moldb-inchikey>WQZGKKKJIJFFOK-PHYPRBDBSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">180.1559</moldb-average-mass>
  <moldb-mono-mass type="decimal">180.063388116</moldb-mono-mass>
  <origin>Endogenous</origin>
  <state>Solid</state>
  <logp>-3.6</logp>
  <hmdb-id>HMDB00143</hmdb-id>
  <chembl-id>CHEMBL1233058</chembl-id>
  <chemspider-id>388480</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference> Avigad, Gad. Synthesis of D-galactose-6-t and D-galactosides-6-t. Carbohydrate Research (1967), 3(4), 430-4.</synthesis-reference>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM003308</chemdb-id>
  <dsstox-id nil="true"/>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id nil="true"/>
  <iupac>(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal</iupac>
  <moldb-polar-surface-area>110.38000000000001</moldb-polar-surface-area>
  <moldb-refractivity>35.9234</moldb-refractivity>
  <moldb-polarizability>16.129783718715995</moldb-polarizability>
  <moldb-rotatable-bond-count>1</moldb-rotatable-bond-count>
  <moldb-acceptor-count>6</moldb-acceptor-count>
  <moldb-donor-count>5</moldb-donor-count>
  <moldb-pka-strongest-acidic>11.298101552080594</moldb-pka-strongest-acidic>
  <moldb-pka-strongest-basic>-2.9810792051782764</moldb-pka-strongest-basic>
  <moldb-physiological-charge>0</moldb-physiological-charge>
  <moldb-number-of-rings>1</moldb-number-of-rings>
  <moldb-alogps-logp>-2.57</moldb-alogps-logp>
  <moldb-alogps-logs>0.64</moldb-alogps-logs>
  <moldb-alogps-solubility>7.82e+02 g/l</moldb-alogps-solubility>
</compound>
