CC(C)C1=CC=C(C=C1)C(CC(=O)C1=CC=CC=C1)C(C(O)=O)C1=CC=CC=C1

InChIKey=MDTBRRQJXPODOI-UHFFFAOYSA-N

C26H26O3

386.491

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Retro-dihydrochalcones Stilbenes Alkyl-phenylketones Phenylpropanoic acids Butyrophenones Aromatic monoterpenoids Monocyclic monoterpenoids Phenylpropanes Cumenes Benzoyl derivatives Aryl alkyl ketones Medium-chain fatty acids Carboxylic acids Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Norlignan skeleton - Retro-dihydrochalcone - Linear 1,3-diarylpropanoid - Stilbene - Alkyl-phenylketone - Butyrophenone - 3-phenylpropanoic-acid - P-cymene - Aromatic monoterpenoid - Monocyclic monoterpenoid - Monoterpenoid - Phenylketone - Cumene - Phenylpropane - Benzoyl - Aryl alkyl ketone - Aryl ketone - Medium-chain fatty acid - Fatty acid - Fatty acyl - Benzenoid - Monocyclic benzene moiety - Ketone - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - 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