89691 <common-name>17ß,19-Dihydroxyandrost-4-en-3-one 17-benzoate</common-name> <description>17ß,19-Dihydroxyandrost-4-en-3-one 17-benzoate belongs to the steroid esters, a subclass of steroids and steroid derivatives within the organic compounds. It is categorized under the superclass of lipids and lipid-like molecules. The compound has the formula C26H32O4 and an average molecular weight of 408.54 g/mol.</description> <cas nil="true"/> <pubchem-id>22827731</pubchem-id> <chemical-formula>C26H32O4</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">2026-04-04T23:53:21Z</created-at> <updated-at type="dateTime">2026-04-04T23:53:21Z</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>CC12CCC3C(CCC4=CC(=O)CCC34CO)C1CCC2OC(=O)C1=CC=CC=C1</moldb-smiles> <moldb-formula>C26H32O4</moldb-formula> <moldb-inchi>InChI=1/C26H32O4/c1-25-13-12-22-20(8-7-18-15-19(28)11-14-26(18,22)16-27)21(25)9-10-23(25)30-24(29)17-5-3-2-4-6-17/h2-6,15,20-23,27H,7-14,16H2,1H3</moldb-inchi> <moldb-inchikey>OSPYUOYEOOYDPK-NVRZZMOUSA-N</moldb-inchikey> <moldb-average-mass type="decimal">408.538</moldb-average-mass> <moldb-mono-mass type="decimal">408.2300595</moldb-mono-mass> <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>CHEM085584</chemdb-id> <dsstox-id>DTXSID30942202</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00050626</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>Lipids and lipid-like molecules</superklass> <klass>Steroids and steroid derivatives</klass> <subklass>Steroid esters</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0114461</sync-id> <structure-inchikey>OSPYUOYEOOYDPK-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>888000400000000040000000020000000002000020400000000000000020000000008000000004000080000800000000000180000080010040000000200000000002000200000020000000000100000000000000000000000000010000000040000000000000000008020000000000000000000000100000000048000000810000000200000000200000000100200000000000000020020000000004000000000040084000000400000000000000040000000000000000000000000000000000400000000000000000000000000000200200000010020000000000000000000040000000000400000001000000004000000800000000</structure-fingerprint> 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