COC1=CC=C(NC(=CC(=O)C2=CC=CC=C2)C(=O)C2=CC=CC=C2)C=C1

InChIKey=CFTXUSBBDUWMBA-UHFFFAOYSA-N

C23H19NO3

357.409

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Aminophenyl ethers Methoxyanilines Anisoles Aryl ketones Benzoyl derivatives Phenoxy compounds Methoxybenzenes Alkyl aryl ethers Alpha-branched alpha,beta-unsaturated ketones Alpha-amino ketones Acryloyl compounds Enones Vinylogous amides Enamines Hydrocarbon derivatives Organic oxides

Aromatic homomonocyclic compounds

Norlignan skeleton - Methoxyaniline - Aminophenyl ether - Anisole - Benzoyl - Phenol ether - Aryl ketone - Aniline or substituted anilines - Phenoxy compound - Methoxybenzene - Alkyl aryl ether - Alpha-branched alpha,beta-unsaturated-ketone - Monocyclic benzene moiety - Benzenoid - Alpha,beta-unsaturated ketone - Acryloyl-group - Vinylogous amide - Enone - Alpha-aminoketone - Ketone - Ether - Enamine - Organic oxygen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aromatic homomonocyclic 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