COC1=C(O)C2=C3C(CCN=C3CC3=CC=C(OC4=C(O)C=CC(CC5=NCCC6=CC(OC)=C(O2)C=C56)=C4)C=C3)=C1

InChIKey=YOHLJCJAHBBOFL-UHFFFAOYSA-N

C34H30N2O6

562.622

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Diarylethers Dihydroisoquinolines Anisoles Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Ketimines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Oxyneolignan skeleton - Diaryl ether - Dihydroisoquinoline - Anisole - Phenol ether - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Ketimine - Oxacycle - Ether - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Imine - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - 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