COC(=O)CC(CCC1=CC=C(NS(=O)(=O)C2=CC=CC=C2)C=C1)C1=CC=CC(=C1)C(N)=N

InChIKey=GKIMFPDOQSVZBN-UHFFFAOYSA-N

C25H27N3O4S

465.57

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Linear 1,3-diarylpropanoids Sulfanilides Benzenesulfonamides Benzenesulfonyl compounds Fatty acid methyl esters Organosulfonamides Methyl esters Aminosulfonyl compounds Monocarboxylic acids and derivatives Carboximidamides Carboxamidines Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic homomonocyclic compounds

Norlignan skeleton - Linear 1,3-diarylpropanoid - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Fatty acid ester - Fatty acid methyl ester - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Organosulfonic acid amide - Methyl ester - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Carboxylic acid ester - Amidine - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Carboxylic acid amidine - Carboximidamide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organic oxygen compound - 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