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<compound>
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  <common-name>[3,5-dioxo-4-(3-oxobutyl)-1,2-diphenylpyrazolidin-4-yl]methyl 2-phenylacetate</common-name>
  <description nil="true"/>
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  <pubchem-id>3039098</pubchem-id>
  <chemical-formula>C28H26N2O5</chemical-formula>
  <weight>470.5</weight>
  <appearance nil="true"/>
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  <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">2026-08-31T11:43:49Z</created-at>
  <updated-at type="dateTime">2026-08-31T11:43:49Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia nil="true"/>
  <uniprot-id nil="true"/>
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  <omim-id nil="true"/>
  <chebi-id nil="true"/>
  <biocyc-id nil="true"/>
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  <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>CC(=O)CCC1(C(=O)N(N(C1=O)C2=CC=CC=C2)C3=CC=CC=C3)COC(=O)CC4=CC=CC=C4</moldb-smiles>
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  <origin nil="true"/>
  <state nil="true"/>
  <logp>3.8</logp>
  <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>CHEM343777</chemdb-id>
  <dsstox-id nil="true"/>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id nil="true"/>
  <iupac>[3,5-dioxo-4-(3-oxobutyl)-1,2-diphenylpyrazolidin-4-yl]methyl 2-phenylacetate</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>Benzenoids</superklass>
  <klass>Benzene and substituted derivatives</klass>
  <subklass nil="true"/>
  <paper-count type="integer" nil="true"/>
  <sync-id>CED0298220</sync-id>
  <structure-inchikey>FDMZYKFWFOKYGX-UHFFFAOYSA-N</structure-inchikey>
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  <structure-pattern-fingerprint>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</structure-pattern-fingerprint>
  <structure-pickle>ï¾­Þ����������������#���&amp;���€���`�������(�������(�������`�������`������� ������(�������(�������(�������(�������(�������(������@(������@h�������@h�������@h�������@h�������@h�������@(������@h�������@h�������@h�������@h�������@h��������`�������(�������(�������(�������`������@(������@h�������@h�������@h�������@h�������@h����������������������������(��� �	�	
 
�(�	� �h��h���h���h���h��� ��h���h���h���h���h��������� ��(���������h���h�� h� !h�!"h�
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	����������������� !"�����������</structure-pickle>
  <structure-indexed-at type="dateTime">2026-09-19T05:46:26Z</structure-indexed-at>
</compound>
