[H][C@@](CC(O)=O)(C=C(C1=CC=CC=C1)C1=CC=CC=C1)C1=C(C)C=C(C)C=C1C

InChIKey=VAMMKVBFILUKHR-QHCPKHFHSA-N

C26H26O2

370.492

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Linear 1,3-diarylpropanoids Diphenylmethanes Phenylpropanoic acids Monocyclic monoterpenoids Aromatic monoterpenoids Styrenes Medium-chain fatty acids Unsaturated fatty acids Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic homomonocyclic compounds

Norlignan skeleton - Linear 1,3-diarylpropanoid - Diphenylmethane - 3-phenylpropanoic-acid - P-cymene - Aromatic monoterpenoid - Monoterpenoid - Monocyclic monoterpenoid - Medium-chain fatty acid - Styrene - Monocyclic benzene moiety - Fatty acyl - Fatty acid - Benzenoid - Unsaturated fatty acid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Organooxygen 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.

Not available