OC[C@H](CC1=CC=C(OCC2=CC=CC=C2)C=C1)NC(=O)C[C@H]1CC=CC[C@H](CC2=CC=CC=C2)C(=O)OC[C@H](COCC2=CC=CC=C2)NC1=O

InChIKey=AMABIXJTEDTIGE-AJWAGCPHSA-N

C43H48N2O7

704.864

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Amphetamines and derivatives Benzylethers Phenoxy compounds Phenol ethers Alkyl aryl ethers Secondary carboxylic acid amides Lactones Lactams Carboxylic acid esters Oxacyclic compounds Azacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Hydrocarbon derivatives Carbonyl compounds Organic oxides Organonitrogen compounds Organopnictogen compounds Primary alcohols

Aromatic heteromonocyclic compounds

Macrolactam - Amphetamine or derivatives - Benzylether - Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Secondary carboxylic acid amide - Carboxylic acid derivative - Oxacycle - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic oxide - Primary alcohol - Carbonyl group - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

Not available