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  <common-name>6-[(4,6-Dimethylpyrimidin-2-yl)sulfanyl]-3-(heptafluoropropyl)[1,2,4]triazolo[4,3-b]pyridazine</common-name>
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  <pubchem-id>549237</pubchem-id>
  <chemical-formula>C14H9F7N6S</chemical-formula>
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  <density nil="true"/>
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  <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">2026-04-06T05:13:34Z</created-at>
  <updated-at type="dateTime">2026-08-28T10:30:55Z</updated-at>
  <interacting-proteins nil="true"/>
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  <uniprot-id nil="true"/>
  <kegg-compound-id nil="true"/>
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  <chebi-id nil="true"/>
  <biocyc-id nil="true"/>
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  <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>CC1=CC(C)=NC(SC2=NN3C(C=C2)=NN=C3C(F)(F)C(F)(F)C(F)(F)F)=N1</moldb-smiles>
  <moldb-formula>C14H9F7N6S</moldb-formula>
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  <origin nil="true"/>
  <state nil="true"/>
  <logp>3.8</logp>
  <hmdb-id nil="true"/>
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  <biodb-id nil="true"/>
  <synthesis-reference nil="true"/>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM117818</chemdb-id>
  <dsstox-id>DTXSID00896283</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00109043</susdat-id>
  <iupac>6-[(4,6-Dimethylpyrimidin-2-yl)sulfanyl]-3-(heptafluoropropyl)[1,2,4]triazolo[4,3-b]pyridazine</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>Organosulfur compounds</superklass>
  <klass>Thioethers</klass>
  <subklass>Aryl thioethers</subklass>
  <paper-count type="integer">0</paper-count>
  <sync-id>CED0104300</sync-id>
  <structure-inchikey>FVSATDQRASQLEK-UHFFFAOYSA-N</structure-inchikey>
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  <structure-pickle>ï¾­Þ������������������������€���`������@(������@h�������@(�������`������@(������@(������� �����@(������@(������@(������@(������@h�������@h�������@(������@(������@(������� ����	� ����	� ������ ����	� ����	� ������ ����	� ����	� ����	� �����@(�����������h���h������h���h��������	h�	
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  <structure-indexed-at type="dateTime">2026-09-19T04:45:13Z</structure-indexed-at>
</compound>
