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<compound>
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  <common-name>3-methyl-5-phenylmethoxy-n'-propan-2-yl-1h-indole-2-carbohydrazide</common-name>
  <description nil="true"/>
  <cas nil="true"/>
  <pubchem-id>43849</pubchem-id>
  <chemical-formula>C20H23N3O2</chemical-formula>
  <weight>337.4</weight>
  <appearance nil="true"/>
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  <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">2026-08-29T22:52:03Z</created-at>
  <updated-at type="dateTime">2026-08-29T22:52:03Z</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>CC1=C(NC2=C1C=C(C=C2)OCC3=CC=CC=C3)C(=O)NNC(C)C</moldb-smiles>
  <moldb-formula>C20H23N3O2</moldb-formula>
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  <origin nil="true"/>
  <state nil="true"/>
  <logp>4.1</logp>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id nil="true"/>
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  <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>CHEM318514</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-methyl-5-phenylmethoxy-n'-propan-2-yl-1h-indole-2-carbohydrazide</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>Organoheterocyclic compounds</superklass>
  <klass>Indoles and derivatives</klass>
  <subklass>Indolecarboxylic acids and derivatives</subklass>
  <paper-count type="integer" nil="true"/>
  <sync-id>CED0273323</sync-id>
  <structure-inchikey>RLJOFJVMMNUCPH-UHFFFAOYSA-N</structure-inchikey>
  <structure-fingerprint>40000000000000080000800000100100000000000000000000000000000000080008001000000000200000000000000004000000000000000080001002000000000000000000000000000000000000000022000010000100000200002040000000000000010000000000000000100000000000000000000000000000000000000800000040200000800000200000000080000000000100000000000000000000200010000000000000040000080000000001004000280000000000040000000000000000000000000000000000000000000000000000002000004220000000000000000000000000000040000000000400001400000000000000000000000020</structure-fingerprint>
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  <structure-pickle>ï¾­Þ������������������������€���`������@(������@(������@8�������@(������@(������@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�B��������������	������������������</structure-pickle>
  <structure-indexed-at type="dateTime">2026-09-19T05:27:06Z</structure-indexed-at>
</compound>
