CC(C)(C)C1=CC=C(COC2=CC=CC=C2\C=C\C(CCCCC(O)=O)CC2=CC=C(C=C2)C2=NNN=N2)C=C1

InChIKey=GUZUKHAXEFOXRL-SFQUDFHCSA-N

C33H38N4O3

538.692

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Phenyltetrazoles and derivatives Phenylpropanes Medium-chain fatty acids Phenol ethers Phenoxy compounds Styrenes Alkyl aryl ethers Heterocyclic fatty acids Amino fatty acids Branched fatty acids Unsaturated fatty acids Heteroaromatic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic heteromonocyclic compounds

Norlignan skeleton - Phenyltetrazole - Phenylpropane - Phenoxy compound - Phenol ether - Styrene - Medium-chain fatty acid - Alkyl aryl ether - Amino fatty acid - Branched fatty acid - Heterocyclic fatty acid - Monocyclic benzene moiety - Fatty acyl - Fatty acid - Unsaturated fatty acid - Benzenoid - Azole - Tetrazole - Heteroaromatic compound - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organonitrogen compound - Aromatic heteromonocyclic 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