COC1=C2OC3=CC=C(CC4C5=CC(OC6=C7C(CC(C=C1)=C2)[N+](C)(CC([O-])=O)CCC7=CC(OC)=C6OC)=C(OC)C=C5CC[N+]4(C)CC([O-])=O)C=C3

InChIKey=CUSHYNWDBFBRJS-UHFFFAOYSA-N

C42H46N2O10

738.834

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Diarylethers Tetrahydroisoquinolines Alpha amino acids Anisoles Alkyl aryl ethers Aralkylamines Dicarboxylic acids and derivatives Tetraalkylammonium salts Carboxylic acid salts Oxacyclic compounds Azacyclic compounds Carboxylic acids Organic salts Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic cations

Aromatic heteropolycyclic compounds

Oxyneolignan skeleton - Diaryl ether - Alpha-amino acid - Alpha-amino acid or derivatives - Tetrahydroisoquinoline - Anisole - Phenol ether - Alkyl aryl ether - Aralkylamine - Dicarboxylic acid or derivatives - Benzenoid - Tetraalkylammonium salt - Quaternary ammonium salt - Carboxylic acid salt - Carboxylic acid derivative - Oxacycle - Carboxylic acid - Azacycle - Organoheterocyclic compound - Ether - Amine - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic salt - Organonitrogen compound - Organooxygen compound - Organic cation - Aromatic heteropolycyclic 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