CC(C)C1=C(O)C(=O)\C(=C/NC2=CC=C(C=C2)C(O)=O)C2=C(O)C(=C(C)C=C12)C1=C(C)C=C2C(C(C)C)=C(O)C(=O)\C(=C/NC3=CC=C(C=C3)C(O)=O)C2=C1O

InChIKey=FORIMSFSVWQEEG-LZUTUTKMSA-N

C44H40N2O10

756.808

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Sesquiterpenoids Naphthalenes Aminobenzoic acids Benzoic acids Benzoyl derivatives Aniline and substituted anilines 1-hydroxy-4-unsubstituted benzenoids Vinylogous amides Cyclic ketones Enols Enamines Carboxylic acids Organic oxides Hydrocarbon derivatives

Aromatic homopolycyclic compounds

Neolignan skeleton - Cadinane sesquiterpenoid - Sesquiterpenoid - Aminobenzoic acid - Aminobenzoic acid or derivatives - Naphthalene - Benzoic acid or derivatives - Benzoic acid - Benzoyl - Aniline or substituted anilines - Phenol - 1-hydroxy-4-unsubstituted benzenoid - Benzenoid - Monocyclic benzene moiety - Vinylogous amide - Cyclic ketone - Ketone - Enol - Enamine - Carboxylic acid - Carboxylic acid derivative - Organooxygen compound - Carbonyl group - Amine - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Aromatic homopolycyclic 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