<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4470</id>
  <title>T3D4416</title>
  <common-name>Creatinine</common-name>
  <description>Creatinine or creatine anhydride, is a breakdown product of creatine phosphate in muscle. The loss of water molecule from creatine results in the formation of creatinine. Creatinine is transferred to the kidneys by blood plasma, whereupon it is eliminated from the body by glomerular filtration and partial tubular excretion. Creatinine is usually produced at a fairly constant rate by the body. Measuring serum creatinine is a simple test and it is the most commonly used indicator of renal function. A rise in blood creatinine levels is observed only with marked damage to functioning nephrons; therefore this test is not suitable for detecting early kidney disease. The typical reference range for women is considered about 45-90 umol/l, for men 60-110 umol/l. Creatine and creatinine are metabolized in the kidneys, muscle, liver and pancreas.</description>
  <cas>60-27-5</cas>
  <pubchem-id>588</pubchem-id>
  <chemical-formula>C4H7N3O</chemical-formula>
  <weight nil="true"/>
  <appearance>White powder.</appearance>
  <melting-point>303°C (decomposes)</melting-point>
  <boiling-point></boiling-point>
  <density nil="true"/>
  <solubility>80.1 mg/mL at 16°C</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">2014-08-29T06:51:09Z</created-at>
  <updated-at type="dateTime">2026-04-14T18:26:08Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Creatinine</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C00791</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>16737</chebi-id>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB11846</drugbank-id>
  <pdb-id nil="true"/>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CN1CC(=O)NC1=N</moldb-smiles>
  <moldb-formula>C4H7N3O</moldb-formula>
  <moldb-inchi>InChI=1S/C4H7N3O/c1-7-2-3(8)6-4(7)5/h2H2,1H3,(H2,5,6,8)</moldb-inchi>
  <moldb-inchikey>DDRJAANPRJIHGJ-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">113.1179</moldb-average-mass>
  <moldb-mono-mass type="decimal">113.058911861</moldb-mono-mass>
  <origin>Endogenous</origin>
  <state>Solid</state>
  <logp>-1.76</logp>
  <hmdb-id>HMDB00562</hmdb-id>
  <chembl-id>CHEMBL65567</chembl-id>
  <chemspider-id>568</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>Reddick, Rebecca E.; Kenyon, George L. Syntheses and NMR studies of specifically labeled [2-15N]phosphocreatine, [2-15N]creatinine, and related 15N-labeled compounds. Journal of the American Chemical Society (1987), 109(14), 4380-7.</synthesis-reference>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM003376</chemdb-id>
  <dsstox-id>DTXSID8045987</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00009814</susdat-id>
  <iupac>2-imino-1-methylimidazolidin-4-one</iupac>
</compound>
