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<compound>
  <id type="integer">81051</id>
  <title nil="true"/>
  <common-name>4,17-Dihydroxypregn-4-ene-3,20-dione 4-acetate 17-hexanoate</common-name>
  <description>4,17-Dihydroxypregn-4-ene-3,20-dione 4-acetate 17-hexanoate belongs to the pregnane steroids, a subclass of steroids and steroid derivatives within the organic compounds. This lipid and lipid-like molecule has the formula C29H42O6 and an average molecular weight of 486.65 g/mol.</description>
  <cas>94135-06-5</cas>
  <pubchem-id>44146576</pubchem-id>
  <chemical-formula>C29H42O6</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">2026-04-04T17:02:32Z</created-at>
  <updated-at type="dateTime">2026-04-04T17:02:32Z</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>CCCCCC(=O)O[C@@]1(CC[C@H]2[C@@H]3CCC4=C(OC(C)=O)C(=O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)=O</moldb-smiles>
  <moldb-formula>C29H42O6</moldb-formula>
  <moldb-inchi>InChI=1S/C29H42O6/c1-6-7-8-9-25(33)35-29(18(2)30)17-13-22-20-10-11-23-26(34-19(3)31)24(32)14-15-27(23,4)21(20)12-16-28(22,29)5/h20-22H,6-17H2,1-5H3/t20-,21+,22+,27-,28+,29+/m1/s1</moldb-inchi>
  <moldb-inchikey>WRZVFSQVZDEDIK-NTLFILIOSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">486.649</moldb-average-mass>
  <moldb-mono-mass type="decimal">486.298139</moldb-mono-mass>
  <origin nil="true"/>
  <state nil="true"/>
  <logp nil="true"/>
  <hmdb-id nil="true"/>
  <chembl-id nil="true"/>
  <chemspider-id>21166878</chemspider-id>
  <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>CHEM076944</chemdb-id>
  <dsstox-id>DTXSID40240741</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00040134</susdat-id>
  <iupac>[(8R,9S,10R,13S,14S,17R)-17-acetyl-4-acetyloxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl] hexanoate</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>Lipids and lipid-like molecules</superklass>
  <klass>Steroids and steroid derivatives</klass>
  <subklass>Pregnane steroids</subklass>
  <paper-count type="integer">0</paper-count>
  <sync-id>CED0144748</sync-id>
  <structure-inchikey>WRZVFSQVZDEDIK-NTLFILIOSA-N</structure-inchikey>
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  <structure-indexed-at type="dateTime">2026-09-19T04:27:48Z</structure-indexed-at>
</compound>
