COC1=CC=C(C=C1)[C@H]([C@H](C)C(=O)C1=CC=CC=C1O)C(\C)=C(/O)C1=CC=CC=C1O

InChIKey=APJJMPVZJIHPQW-RSKWQERGSA-N

C26H26O5

418.489

Organic compounds

Lignans, neolignans and related compounds

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Lignans, neolignans and related compounds

2'-Hydroxy-dihydrochalcones Cinnamylphenols Alkyl-phenylketones Butyrophenones Phenylpropanes Methoxybenzenes Phenoxy compounds Benzoyl derivatives Aryl alkyl ketones Anisoles 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids Vinylogous acids Enols Hydrocarbon derivatives Organic oxides

Aromatic homomonocyclic compounds

Norlignan skeleton - 2'-hydroxy-dihydrochalcone - Linear 1,3-diarylpropanoid - Cinnamylphenol - Alkyl-phenylketone - Butyrophenone - Phenylpropane - Phenylketone - Phenoxy compound - Benzoyl - Phenol ether - Anisole - Aryl ketone - Aryl alkyl ketone - Methoxybenzene - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - Phenol - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Benzenoid - Vinylogous acid - Ketone - Ether - Enol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - 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.

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