[I-].CC(C)C(O)(C(CN1CC[N+](C)(C)CC1)CC1=CC=CC=C1)C1=CC=CC=C1

InChIKey=LUEHCGUTTUKGRX-UHFFFAOYSA-M

C25H37IN2O

508.488

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Linear 1,3-diarylpropanoids Phenylpropanes N-methylpiperazines Aralkylamines Tetraalkylammonium salts Tertiary alcohols 1,3-aminoalcohols Trialkylamines Azacyclic compounds Organic zwitterions Organic iodide salts Hydrocarbon derivatives Aromatic alcohols

Aromatic heteromonocyclic compounds

Norlignan skeleton - Linear 1,3-diarylpropanoid - Phenylpropane - N-methylpiperazine - N-alkylpiperazine - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Piperazine - 1,4-diazinane - 1,3-aminoalcohol - Tertiary alcohol - Quaternary ammonium salt - Tetraalkylammonium salt - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Aromatic alcohol - Organic zwitterion - Organic salt - Organooxygen compound - Organonitrogen compound - Organic iodide salt - Hydrocarbon derivative - Organic oxygen compound - Amine - Alcohol - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.

Not available