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  <common-name>Methyl 3-methoxy-O,ß-dimethyl-L-tyrosinate</common-name>
  <description nil="true"/>
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  <pubchem-id>21116374</pubchem-id>
  <chemical-formula>C13H19NO4</chemical-formula>
  <weight nil="true"/>
  <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">2026-04-04T21:41:01Z</created-at>
  <updated-at type="dateTime">2026-04-04T21:41:01Z</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>COC(=O)[C@@](C)(N)CC1=CC(OC)=C(OC)C=C1</moldb-smiles>
  <moldb-formula>C13H19NO4</moldb-formula>
  <moldb-inchi>InChI=1/C13H19NO4/c1-8(12(14)13(15)18-4)9-5-6-10(16-2)11(7-9)17-3/h5-8,12H,14H2,1-4H3</moldb-inchi>
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  <origin nil="true"/>
  <state nil="true"/>
  <logp nil="true"/>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id nil="true"/>
  <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 nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM082430</chemdb-id>
  <dsstox-id>DTXSID00941484</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00046894</susdat-id>
  <iupac nil="true"/>
  <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>Amino acids, peptides, and analogues</subklass>
  <paper-count type="integer">0</paper-count>
  <sync-id>CED0075676</sync-id>
  <structure-inchikey>PICGBRAYRQJNGT-ZDUSSCGKSA-N</structure-inchikey>
  <structure-fingerprint>200800200002000000800000000000000000000000000400000000000000200000000000000000000800000000000000000000000000000000000000000000000000000200000000020000010000100000000000000000000000021010000000040000000100080000000000000000000000000000000001000000040100000000000000000000080001020000000000000000400000000000000000000000000000000080000000000000000000000000000000000000080000000000000000000000000000000000000000000200000000220000000000000000000000000000040000000000400000000000020000000000000000000</structure-fingerprint>
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  <structure-pickle>ï¾­Þ������������������������€���`�������(�������(�������(������ $�������`�������`�������`������@(������@h�������@(�������(�������`������@(�������(�������`������@h�������@h������������ ��(�����������������	h�	
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	����������</structure-pickle>
  <structure-indexed-at type="dateTime">2026-09-19T04:30:56Z</structure-indexed-at>
</compound>
