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<compound>
  <id type="integer">118499</id>
  <title nil="true"/>
  <common-name>Echivulgarine</common-name>
  <description>Echivulgarine is an organic compound with the chemical formula C25H37NO8 and an average molecular weight of 479.57 g/mol. Echivulgarine belongs to the tricarboxylic acids and derivatives, a subclass of carboxylic acids and derivatives within the organic compounds.

The substance has been identified in or released from 13 recorded sources across several diverse sectors. Within electrical and electronic equipment, it is found in cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among one other source. In the textiles, leather and furnishings sector, it is associated with synthetic textiles as well as carpets and rugs. It is also present in food packaging within the food, food processing and cookware sector, and in medical devices under healthcare, pharmaceuticals and veterinary products. Additionally, the compound is found in lubricants used in both the energy, oil and gas sector and the industrial manufacturing and chemical processing sector, along with one further sector. Recorded routes of exposure for this compound include inhalation, oral ingestion, and touch.</description>
  <cas nil="true"/>
  <pubchem-id>122214229</pubchem-id>
  <chemical-formula>C25H37NO8</chemical-formula>
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  <appearance nil="true"/>
  <melting-point nil="true"/>
  <boiling-point nil="true"/>
  <density nil="true"/>
  <solubility nil="true"/>
  <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 nil="true"/>
  <use-source nil="true"/>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2026-04-06T01:44:20Z</created-at>
  <updated-at type="dateTime">2026-05-21T01:17:45Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
  <kegg-compound-id nil="true"/>
  <omim-id nil="true"/>
  <chebi-id nil="true"/>
  <biocyc-id nil="true"/>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id nil="true"/>
  <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>[H][C@]1(CCN2CC(COC(=O)[C@@](O)([C@H](C)OC(=O)C(\C)=C/C)C(C)(C)O)=C[C@]12[H])OC(=O)C(\C)=C/C</moldb-smiles>
  <moldb-formula>C25H37NO8</moldb-formula>
  <moldb-inchi>InChI=1S/C25H37NO8/c1-8-15(3)21(27)33-17(5)25(31,24(6,7)30)23(29)32-14-18-12-19-20(10-11-26(19)13-18)34-22(28)16(4)9-2/h8-9,12,17,19-20,30-31H,10-11,13-14H2,1-7H3/b15-8-,16-9-/t17-,19+,20+,25-/m0/s1</moldb-inchi>
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  <moldb-average-mass type="decimal">479.57</moldb-average-mass>
  <moldb-mono-mass type="decimal">479.2519171</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp nil="true"/>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id>95601211</chemspider-id>
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  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM114392</chemdb-id>
  <dsstox-id>DTXSID201020029</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00094187</susdat-id>
  <iupac>(1R,7aR)-6-[({(2R)-2,3-Dihydroxy-3-methyl-2-[(1S)-1-{[(2Z)-2-methylbut-2-enoyl]oxy}ethyl]butanoyl}oxy)methyl]-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-yl (2Z)-2-methylbut-2-enoate</iupac>
  <moldb-polar-surface-area nil="true"/>
  <moldb-refractivity nil="true"/>
  <moldb-polarizability nil="true"/>
  <moldb-rotatable-bond-count nil="true"/>
  <moldb-acceptor-count nil="true"/>
  <moldb-donor-count nil="true"/>
  <moldb-pka-strongest-acidic nil="true"/>
  <moldb-pka-strongest-basic nil="true"/>
  <moldb-physiological-charge nil="true"/>
  <moldb-number-of-rings nil="true"/>
  <moldb-alogps-logp nil="true"/>
  <moldb-alogps-logs nil="true"/>
  <moldb-alogps-solubility nil="true"/>
  <kingdom>Organic compounds</kingdom>
  <superklass>Organic acids and derivatives</superklass>
  <klass>Carboxylic acids and derivatives</klass>
  <subklass>Tricarboxylic acids and derivatives</subklass>
  <paper-count type="integer">9</paper-count>
  <sync-id>CED0036810</sync-id>
  <structure-inchikey>JZEITCZHHKPGHS-LTCADICWSA-N</structure-inchikey>
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  <structure-indexed-at type="dateTime">2026-09-19T04:44:05Z</structure-indexed-at>
</compound>
