<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4653</id>
  <title>T3D4599</title>
  <common-name>Myristic acid</common-name>
  <description>Myristic acid is a saturated 14-carbon fatty acid occurring in most animal and vegetable fats, particularly butterfat and coconut, palm, and nutmeg oils. It is used to synthesize flavor and as an ingredient in soaps and cosmetics. (From Dorland, 28th ed). Myristic acid is also commonly added to a penultimate nitrogen terminus glycine in receptor-associated kinases to confer the membrane localisation of the enzyme. this is achieved by the myristic acid having a high enough hydrophobicity to become incorporated into the fatty acyl core of the phospholipid bilayer of the plasma membrane of the eukaryotic cell.(wikipedia).</description>
  <cas>544-63-8</cas>
  <pubchem-id>11005</pubchem-id>
  <chemical-formula>C14H28O2</chemical-formula>
  <weight>228.37</weight>
  <appearance>White powder.</appearance>
  <melting-point>53.9 °C</melting-point>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility>0.00107 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">2014-09-05T17:12:25Z</created-at>
  <updated-at type="dateTime">2026-04-17T17:40:34Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>Myristic acid</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C06424</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>28875</chebi-id>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB08231</drugbank-id>
  <pdb-id>MYR</pdb-id>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>CCCCCCCCCCCCCC(O)=O</moldb-smiles>
  <moldb-formula>C14H28O2</moldb-formula>
  <moldb-inchi>InChI=1S/C14H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h2-13H2,1H3,(H,15,16)</moldb-inchi>
  <moldb-inchikey>TUNFSRHWOTWDNC-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">228.3709</moldb-average-mass>
  <moldb-mono-mass type="decimal">228.20893014</moldb-mono-mass>
  <origin>Endogenous</origin>
  <state>Solid</state>
  <logp>6.11</logp>
  <hmdb-id>HMDB00806</hmdb-id>
  <chembl-id>CHEMBL111077</chembl-id>
  <chemspider-id>10539</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>Greaves, W. S.; Linstead, R. P.; Shephard, B. R.; Thomas, S. L. S.; Weedon, B. C. L.  Anodic syntheses. I. New syntheses of stearic, myristic, and other acids.    Journal of the Chemical Society  (1950),     3326-30.</synthesis-reference>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM003559</chemdb-id>
  <dsstox-id>DTXSID6021666</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id nil="true"/>
  <iupac>tetradecanoic acid</iupac>
</compound>
