CC(C)[C@@H]1NC(=O)[C@H](CC2=CC(\C=C(/C3=C(N=C1O3)C#N)C1=CC=CC=C1O)=C(OCC1=CC=CC=C1)C=C2)NC(=O)OC(C)(C)C

InChIKey=OTVUZWPSJIJUHJ-JHEODLGVSA-N

C37H38N4O6

634.733

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Alpha amino acids and derivatives Phenol ethers 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Alkyl aryl ethers Benzene and substituted derivatives Oxazoles Heteroaromatic compounds Carbamate esters Secondary carboxylic acid amides Lactams Oxacyclic compounds Nitriles Azacyclic compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds

Aromatic heteropolycyclic compounds

Macrolactam - Alpha-amino acid or derivatives - Phenol ether - Alkyl aryl ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocyclic benzene moiety - Benzenoid - Azole - Oxazole - Heteroaromatic compound - Carbamic acid ester - Secondary carboxylic acid amide - Carboxamide group - Lactam - Azacycle - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Nitrile - Carbonitrile - Ether - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Carbonyl group - Cyanide - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic 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