CC(C)C1=CC=C(C=C1)C(CC(=O)C1=CC=CC=C1)C(C(O)=O)C1=CC=C(C=C1)[N+]([O-])=O

InChIKey=HVBNGCBBUVVMIM-UHFFFAOYSA-N

C26H25NO5

431.488

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 Nitrobenzenes Nitro fatty acids Cumenes Aryl alkyl ketones Benzoyl derivatives Nitroaromatic compounds Medium-chain fatty acids Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Carboxylic acids Monocarboxylic acids and derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Norlignan skeleton - Retro-dihydrochalcone - Linear 1,3-diarylpropanoid - Stilbene - Alkyl-phenylketone - Butyrophenone - 3-phenylpropanoic-acid - Aromatic monoterpenoid - Monocyclic monoterpenoid - Monoterpenoid - P-cymene - Phenylketone - Cumene - Nitro fatty acid - Nitrobenzene - Phenylpropane - Benzoyl - Aryl alkyl ketone - Aryl ketone - Medium-chain fatty acid - Nitroaromatic compound - Monocyclic benzene moiety - Fatty acyl - Fatty acid - Benzenoid - Organic nitro compound - Ketone - C-nitro compound - Carboxylic acid derivative - Carboxylic acid - Organic oxoazanium - Monocarboxylic acid or derivatives - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - 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