CCCCC(O)(C(CC1=CC=CC=C1)C[N+]1(C)CC[N+](C)(C)CC1)C1=CC=CC=C1

InChIKey=ZREZKDCYDMXZFD-UHFFFAOYSA-N

C27H42N2O

410.645

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Linear 1,3-diarylpropanoids N-methylpiperazines Aralkylamines Benzene and substituted derivatives Tetraalkylammonium salts Tertiary alcohols 1,3-aminoalcohols Azacyclic compounds Hydrocarbon derivatives Aromatic alcohols Organic cations

Aromatic heteromonocyclic compounds

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