35930 <common-name>3b,17b-Dihydroxyetiocholane</common-name> <description>3b,17b-Dihydroxyetiocholane belongs to the androstane steroids, a subclass of steroids and steroid derivatives within the organic compounds. This lipid and lipid-like molecule has the formula C19H32O2 and an average molecular weight of 292.46 g/mol.</description> <cas>6038-31-9</cas> <pubchem-id nil="true"/> <chemical-formula>C19H32O2</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">2016-05-26T05:15:19Z</created-at> <updated-at type="dateTime">2026-04-06T12:00:11Z</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>C[C@]12CCC3C(CCC4C[C@@H](O)CC[C@]34C)C1CC[C@@H]2O</moldb-smiles> <moldb-formula>C19H32O2</moldb-formula> <moldb-inchi>InChI=1S/C19H32O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-17,20-21H,3-11H2,1-2H3/t12?,13-,14?,15?,16?,17-,18-,19-/m0/s1</moldb-inchi> <moldb-inchikey>CBMYJHIOYJEBSB-WTVXNACZSA-N</moldb-inchikey> <moldb-average-mass type="decimal">292.4562</moldb-average-mass> <moldb-mono-mass type="decimal">292.240230268</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>CHEM034825</chemdb-id> <dsstox-id nil="true"/> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00122674</susdat-id> <iupac nil="true"/> <moldb-polar-surface-area>40.46</moldb-polar-surface-area> <moldb-refractivity>84.63119999999998</moldb-refractivity> <moldb-polarizability>35.52615455598584</moldb-polarizability> <moldb-rotatable-bond-count>0</moldb-rotatable-bond-count> <moldb-acceptor-count>2</moldb-acceptor-count> <moldb-donor-count>2</moldb-donor-count> <moldb-pka-strongest-acidic>18.2963963211217</moldb-pka-strongest-acidic> <moldb-pka-strongest-basic>-0.7580100340749988</moldb-pka-strongest-basic> <moldb-physiological-charge>0</moldb-physiological-charge> <moldb-number-of-rings>4</moldb-number-of-rings> <moldb-alogps-logp>3.56</moldb-alogps-logp> <moldb-alogps-logs>-4.18</moldb-alogps-logs> <moldb-alogps-solubility>1.93e-02 g/l</moldb-alogps-solubility> <kingdom>Organic compounds</kingdom> <superklass>Lipids and lipid-like molecules</superklass> <klass>Steroids and steroid derivatives</klass> <subklass>Androstane steroids</subklass> <paper-count type="integer">4</paper-count> <sync-id>CED0044197</sync-id> <structure-inchikey>CBMYJHIOYJEBSB-WTVXNACZSA-N</structure-inchikey> 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