OC(=O)CCNC(=O)C1=CC=C(C=C1)C(=O)C(=CC(=O)C1=CC=C(OC(F)(F)F)C=C1)C1=CC=C(OC2=CC=CC=C2)C=C1

InChIKey=OLWMDXNMNCZYCG-UHFFFAOYSA-N

C33H24F3NO7

603.55

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Retrochalcones Stilbenes Diphenylethers Cinnamic acids and derivatives Beta amino acids and derivatives Diarylethers Benzamides Aryl ketones Benzoyl derivatives Styrenes Phenoxy compounds Phenol ethers Alpha-branched alpha,beta-unsaturated ketones Enones Acryloyl compounds Trihalomethanes Secondary carboxylic acid amides Carboxylic acids Monocarboxylic acids and derivatives Alkyl fluorides Hydrocarbon derivatives Organic oxides Organofluorides Organonitrogen compounds

Aromatic homomonocyclic compounds

Norlignan skeleton - Retrochalcone - Linear 1,3-diarylpropanoid - Stilbene - Diphenylether - Cinnamic acid or derivatives - Diaryl ether - Beta amino acid or derivatives - Benzamide - Benzoic acid or derivatives - Phenoxy compound - Phenol ether - Benzoyl - Styrene - Aryl ketone - Alpha-branched alpha,beta-unsaturated-ketone - Benzenoid - Monocyclic benzene moiety - Acryloyl-group - Enone - Alpha,beta-unsaturated ketone - Trihalomethane - Carboxamide group - Secondary carboxylic acid amide - Ketone - Ether - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Carboxylic acid - Organohalogen compound - Alkyl halide - Organooxygen compound - Alkyl fluoride - Carbonyl group - Hydrocarbon derivative - Halomethane - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Organofluoride - Organonitrogen compound - 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