<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4523</id>
  <title>T3D4469</title>
  <common-name>Dihydroxyacetone phosphate</common-name>
  <description>Dihydroxyacetone phosphate is an important intermediate in lipid biosynthesis and in glycolysis.</description>
  <cas>57-04-5</cas>
  <pubchem-id>668</pubchem-id>
  <chemical-formula>C3H7O6P</chemical-formula>
  <weight nil="true"/>
  <appearance>White powder.</appearance>
  <melting-point></melting-point>
  <boiling-point></boiling-point>
  <density nil="true"/>
  <solubility></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">2014-08-29T06:51:34Z</created-at>
  <updated-at type="dateTime">2026-05-14T18:07:38Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Dihydroxyacetone phosphate</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C00111</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>16108</chebi-id>
  <biocyc-id>DIHYDROXY-ACETONE-PHOSPHATE</biocyc-id>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB04326</drugbank-id>
  <pdb-id>13P</pdb-id>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>OCC(=O)COP(O)(O)=O</moldb-smiles>
  <moldb-formula>C3H7O6P</moldb-formula>
  <moldb-inchi>InChI=1S/C3H7O6P/c4-1-3(5)2-9-10(6,7)8/h4H,1-2H2,(H2,6,7,8)</moldb-inchi>
  <moldb-inchikey>GNGACRATGGDKBX-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">170.0578</moldb-average-mass>
  <moldb-mono-mass type="decimal">169.998024468</moldb-mono-mass>
  <origin>Endogenous</origin>
  <state>Solid</state>
  <logp>-1.7</logp>
  <hmdb-id>HMDB01473</hmdb-id>
  <chembl-id>CHEMBL1161998</chembl-id>
  <chemspider-id>648</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></synthesis-reference>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM003429</chemdb-id>
  <dsstox-id>DTXSID6058768</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id nil="true"/>
  <iupac>(3-hydroxy-2-oxopropoxy)phosphonic acid</iupac>
  <moldb-polar-surface-area>104.06</moldb-polar-surface-area>
  <moldb-refractivity>30.472099999999998</moldb-refractivity>
  <moldb-polarizability>12.641516377396067</moldb-polarizability>
  <moldb-rotatable-bond-count>4</moldb-rotatable-bond-count>
  <moldb-acceptor-count>5</moldb-acceptor-count>
  <moldb-donor-count>3</moldb-donor-count>
  <moldb-pka-strongest-acidic>1.1902795898513006</moldb-pka-strongest-acidic>
  <moldb-pka-strongest-basic>-3.3227461112640855</moldb-pka-strongest-basic>
  <moldb-physiological-charge>-2</moldb-physiological-charge>
  <moldb-number-of-rings>0</moldb-number-of-rings>
  <moldb-alogps-logp>-1.49</moldb-alogps-logp>
  <moldb-alogps-logs>-0.89</moldb-alogps-logs>
  <moldb-alogps-solubility>2.19e+01 g/l</moldb-alogps-solubility>
</compound>
