103574 <common-name>[5-(4-Fluorophenyl)-1-pentyl-1H-pyrrol-3-yl](naphthalen-1-yl)methanone</common-name> <description>[5-(4-Fluorophenyl)-1-pentyl-1H-pyrrol-3-yl](naphthalen-1-yl)methanone belongs to the naphthalenecarboxylic acids and derivatives, a subclass of naphthalenes within the organic compounds. This benzenoid compound has the chemical formula C26H24FNO and an average molecular weight of 385.48 g/mol.</description> <cas nil="true"/> <pubchem-id nil="true"/> <chemical-formula>C26H24FNO</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">2026-04-05T10:44:55Z</created-at> <updated-at type="dateTime">2026-04-05T10:44:55Z</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>CCCCCN1C=C(C=C1C1=CC=C(F)C=C1)C(=O)C1=CC=CC2=CC=CC=C12</moldb-smiles> <moldb-formula>C26H24FNO</moldb-formula> <moldb-inchi>InChI=1S/C26H24FNO/c1-2-3-6-16-28-18-21(17-25(28)20-12-14-22(27)15-13-20)26(29)24-11-7-9-19-8-4-5-10-23(19)24/h4-5,7-15,17-18H,2-3,6,16H2,1H3</moldb-inchi> <moldb-inchikey>PJCIYIFHTDCK-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">385.482</moldb-average-mass> <moldb-mono-mass type="decimal">385.1841926</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>CHEM099467</chemdb-id> <dsstox-id>DTXSID20658825</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00067996</susdat-id> <iupac>[5-(4-Fluorophenyl)-1-pentyl-1H-pyrrol-3-yl](naphthalen-1-yl)methanone</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>Benzenoids</superklass> <klass>Naphthalenes</klass> <subklass>Naphthalenecarboxylic acids and derivatives</subklass> <paper-count type="integer">2</paper-count> <sync-id>CED0053751</sync-id> <structure-inchikey>PJNACIYIFHTDCK-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>40000000000000000080200000000000000000000000000000000400000200000000000200000000000000000000000000000000000000000080000000000000000000000000000001000000000000002000000000001000000000000000000000002041000000000000000010000480000000011000000000000000000000000100004000000180008000000000401080000000010000000000000000000000000000000000400004000008400000200002000b010000000000000000000000000000040000000000001000000000020000080000000000000200000000000000000000000001000040020000010400800000000000000100000000000000</structure-fingerprint> 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