43686 <common-name>clindamycinsulfoxid</common-name> <description>Clindamycinsulfoxid has the formula C18H33ClN2O6S and an average molecular weight of 440.98 g/mol. Clindamycinsulfoxid belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds.</description> <cas>22431-46-5</cas> <pubchem-id>73046007</pubchem-id> <chemical-formula>C18H33ClN2O6S</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">2016-06-03T09:59:19Z</created-at> <updated-at type="dateTime">2026-03-27T00:38:18Z</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>CCCC1CC(N(C)C1)C(=O)NC(C(C)Cl)C1OC(C(O)C(O)C1O)S(C)=O</moldb-smiles> <moldb-formula>C18H33ClN2O6S</moldb-formula> <moldb-inchi>InChI=1S/C18H33ClN2O6S/c1-5-6-10-7-11(21(3)8-10)17(25)20-12(9(2)19)16-14(23)13(22)15(24)18(27-16)28(4)26/h9-16,18,22-24H,5-8H2,1-4H3,(H,20,25)</moldb-inchi> <moldb-inchikey>XSLGFIQRVCXUEU-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">440.98</moldb-average-mass> <moldb-mono-mass type="decimal">440.1747857</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp nil="true"/> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>9836904</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>CHEM042581</chemdb-id> <dsstox-id>DTXSID60675773</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin>Oertel et al., Poster RISKWa-Fachtagung</stoff-ident-origin> <stoff-ident-id>SI00000616</stoff-ident-id> <susdat-id>NS00006177</susdat-id> <iupac nil="true"/> <moldb-polar-surface-area>119.33000000000001</moldb-polar-surface-area> <moldb-refractivity>107.32000000000004</moldb-refractivity> <moldb-polarizability>45.39555551785246</moldb-polarizability> <moldb-rotatable-bond-count>7</moldb-rotatable-bond-count> <moldb-acceptor-count>7</moldb-acceptor-count> <moldb-donor-count>4</moldb-donor-count> <moldb-pka-strongest-acidic>12.191328836561198</moldb-pka-strongest-acidic> <moldb-pka-strongest-basic>6.851888334762812</moldb-pka-strongest-basic> <moldb-physiological-charge>1</moldb-physiological-charge> <moldb-number-of-rings>2</moldb-number-of-rings> <moldb-alogps-logp>1.01</moldb-alogps-logp> <moldb-alogps-logs>-1.57</moldb-alogps-logs> <moldb-alogps-solubility>1.20e+01 g/l</moldb-alogps-solubility> <kingdom>Organic compounds</kingdom> <superklass>Organic acids and derivatives</superklass> <klass>Carboxylic acids and derivatives</klass> <subklass>Amino acids, peptides, and analogues</subklass> <paper-count type="integer">0</paper-count> <sync-id>CED0150212</sync-id> <structure-inchikey>XSLGFIQRVCXUEU-UHFFFAOYSA-N</structure-inchikey> 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