COC1=CC(=CC(OC)=C1O)[C@@H](O)C(COC(=O)CC(C)C)OC1=C(OC)C=C(\C=C\COC(=O)CC(C)C)C=C1OC

InChIKey=XEANKIUMNPSAJK-GQNRPDPSSA-N

C32H44O11

604.693

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Methoxyphenols Dimethoxybenzenes Styrenes Phenoxy compounds Anisoles Fatty acid esters Alkyl aryl ethers Dicarboxylic acids and derivatives Secondary alcohols Carboxylic acid esters Organic oxides Hydrocarbon derivatives Carbonyl compounds Aromatic alcohols

Aromatic homomonocyclic compounds

Neolignan skeleton - Methoxyphenol - Dimethoxybenzene - M-dimethoxybenzene - Anisole - Phenoxy compound - Phenol ether - Styrene - Methoxybenzene - Phenol - Alkyl aryl ether - Fatty acid ester - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Dicarboxylic acid or derivatives - Secondary alcohol - Carboxylic acid ester - Carboxylic acid derivative - Ether - Organooxygen compound - Aromatic alcohol - Carbonyl group - Alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - 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