103312 <common-name>(-)-Nuciferine</common-name> <description>(-)-Nuciferine is an organic compound with the chemical formula C19H21NO2 and an average molecular weight of 295.38 g/mol. (-)-Nuciferine belongs to the aporphines, a class of alkaloids and derivatives within the organic compounds. This compound is found in or released from 22 recorded sources across several sectors. Within the electrical and electronic equipment sector, it is associated with cell phones, capacitors, wires and cables, batteries, and printed circuit boards, among two other sources. In the food, food processing and cookware sector, it is linked to food packaging, food preservation, the preparation of vinegar, the preparation of wine or sparkling wine, and fermentation processes for beer, as well as one additional source. It is also found in the textiles, leather and furnishings sector, specifically in carpets, rugs, and synthetic textiles. Further recorded sources include household cleaning and consumer products, such as soap detergents and cigar cigarettes. The compound is also identified in drinking water and water supply, as well as in medical devices within the healthcare, pharmaceuticals and veterinary products sector, along with three other sectors. Recorded routes of exposure for (-)-Nuciferine include inhalation, oral ingestion, and touch.</description> <cas>475-83-2</cas> <pubchem-id>10146</pubchem-id> <chemical-formula>C19H21NO2</chemical-formula> <weight>295.4</weight> <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">2026-04-05T10:24:29Z</created-at> <updated-at type="dateTime">2026-08-20T03:11:41Z</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>[H][C@@]12CC3=CC=CC=C3C3=C1C(CCN2C)=CC(OC)=C3OC</moldb-smiles> <moldb-formula>C19H21NO2</moldb-formula> <moldb-inchi>InChI=1S/C19H21NO2/c1-20-9-8-13-11-16(21-2)19(22-3)18-14-7-5-4-6-12(14)10-15(20)17(13)18/h4-7,11,15H,8-10H2,1-3H3/t15-/m1/s1</moldb-inchi> <moldb-inchikey>ORJVQPIHKOARKV-OAHLLOKOSA-N</moldb-inchikey> <moldb-average-mass type="decimal">295.382</moldb-average-mass> <moldb-mono-mass type="decimal">295.1572289</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>3.4</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>9740</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>CHEM099205</chemdb-id> <dsstox-id>DTXSID40963862</dsstox-id> <toxcast-id nil="true"/> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00067009</susdat-id> <iupac>(9R)-15,16-dimethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(17),2,4,6,13,15-hexaene</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>Alkaloids and derivatives</superklass> <klass>Aporphines</klass> <subklass nil="true"/> <paper-count type="integer">1209</paper-count> <sync-id>CED0008001</sync-id> <structure-inchikey>ORJVQPIHKOARKV-OAHLLOKOSA-N</structure-inchikey> <structure-fingerprint>400000014000400000000000000000000400008000000000000000000800000000000002000000040000000000000000000000000000000000000000000100000000000000000000000000000000000040000000100000000000020100000000000080000010100000000040000000800000000000004000000000000100000000080000000000000000008000000000000000080080000000040000000000008400000000000080000000000000010000000000008000004000000008000000201200000000000010000000000000000040008800000000000000000020000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>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</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ������������������������€�� 4��������`������@(������@h�������@h�������@h�������@h�������@(������@(������@(������@(�������`�������`������� ������`������@h�������@(�������(�������`������@(�������(�������`��������������h���h���h���h���h��� � h� h� ������ � �� �h���h��� �����h��� ��� �� ����h���h�B��������� ����������� � ����� ����������</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:40:53Z</structure-indexed-at> </compound>