CN(C)C1=C(C=CC(CC2SC(=O)NC2=O)=C1)C1=CC2=C(C=C1C)C(C)(C)CCC2(C)C

InChIKey=FOEGXADXCZJDNB-UHFFFAOYSA-N

C27H34N2O2S

450.64

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Phenylnaphthalenes Tetralins Dialkylarylamines Aniline and substituted anilines Thiazolidinediones Dicarboximides Thiocarbamic acid derivatives Amino acids and derivatives Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteropolycyclic compounds

Neolignan skeleton - Phenylnaphthalene - Tetralin - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Thiazolidinedione - Monocyclic benzene moiety - Benzenoid - Thiazolidine - Dicarboximide - Amino acid or derivatives - Thiocarbamic acid derivative - Tertiary amine - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Amine - 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