C[N@@+]1([O-])CCC2=CC(O)=C3OC4=C5OC3=C2[C@@H]1CC1=CC(OC2=C(O)C=CC(CC3=NCCC(=C4)C3=C5)=C2)=CC=C1

InChIKey=ODWQPETWLJQNIG-YQPGIBNTSA-N

C33H28N2O6

548.595

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Dibenzo-p-dioxins Diarylethers Tetrahydroisoquinolines Dihydroisoquinolines 1-hydroxy-2-unsubstituted benzenoids Trialkyl amine oxides Ketimines Trisubstituted amine oxides and derivatives Oxacyclic compounds Azacyclic compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations

Aromatic heteropolycyclic compounds

Oxyneolignan skeleton - Dibenzo-p-dioxin - Diaryl ether - Dihydroisoquinoline - Tetrahydroisoquinoline - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Trialkyl amine oxide - Ketimine - N-oxide - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Trisubstituted n-oxide - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Imine - Organooxygen compound - Organic oxygen compound - Organic oxide - Organic salt - 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