COC1=CC(OC)=C(C=C1)C(=O)[C@@H](C)C1=CC=C(CC(C)C)C=C1

InChIKey=UVHJXEPTGFQBHN-HNNXBMFYSA-N

C21H26O3

326.436

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Alpha-methyldeoxybenzoin flavonoids Stilbenes Alkyl-phenylketones Monocyclic monoterpenoids Dimethoxybenzenes Aromatic monoterpenoids Phenylpropanes Phenoxy compounds Benzoyl derivatives Aryl alkyl ketones Anisoles Alkyl aryl ethers Organic oxides Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Alpha-methyldeoxybenzoin flavonoid - Neolignan skeleton - Stilbene - Alkyl-phenylketone - P-cymene - Aromatic monoterpenoid - Monocyclic monoterpenoid - M-dimethoxybenzene - Dimethoxybenzene - Monoterpenoid - Phenylketone - Phenylpropane - Phenoxy compound - Anisole - Benzoyl - Methoxybenzene - Aryl alkyl ketone - Phenol ether - Aryl ketone - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Ketone - Ether - 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