CC1=CC=C(C=C1)C(N1N=NC2=CC=CC=C12)=C(CC(=O)C1=CC=CC=C1)C1=CC=CC=C1

InChIKey=AOLLZMZJQLGAOY-UHFFFAOYSA-N

C29H23N3O

429.523

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 Butyrophenones Benzotriazoles Benzoyl derivatives Aryl alkyl ketones Toluenes Triazoles Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Norlignan skeleton - Retro-dihydrochalcone - Linear 1,3-diarylpropanoid - Stilbene - Alkyl-phenylketone - Butyrophenone - Phenylketone - Benzotriazole - Benzoyl - Aryl alkyl ketone - Aryl ketone - Toluene - Monocyclic benzene moiety - Benzenoid - Azole - Heteroaromatic compound - Triazole - 1,2,3-triazole - Ketone - Organoheterocyclic compound - Azacycle - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic 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