NC(N)=NC1=CC=C(C=C1)C(=O)C1(C=CC=N1)C1=CC2=C(OCC(CC(O)=O)C2)C=C1

InChIKey=JUPHBCWHOWCVMD-UHFFFAOYSA-N

C23H22N4O4

418.453

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Stilbenes Alkyl-phenylketones 1-benzopyrans Benzoyl derivatives Aryl alkyl ketones Alkyl aryl ethers Guanidines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organic oxides Imines Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Neolignan skeleton - Stilbene - Alkyl-phenylketone - Chromane - Benzopyran - 1-benzopyran - Phenylketone - Benzoyl - Aryl alkyl ketone - Aryl ketone - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Guanidine - Ketone - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Ether - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Organic oxide - Hydrocarbon derivative - Imine - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - 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