CC(C)[C@H]1NC(=O)[C@@H](N)CC2=CC([C@@H](O)[C@@](O)(C3=C(N=C1O3)C#N)C1=CC=CC=C1OCC1=CC=CC=C1)=C(OCC1=CC=CC=C1)C=C2

InChIKey=MBQYWEISEIKBLT-RWPCCXGOSA-N

C39H38N4O6

658.755

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Alpha amino acid amides Phenoxy compounds Phenol ethers Alkyl aryl ethers Aralkylamines Tertiary alcohols Oxazoles Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols 1,2-diols Lactams Oxacyclic compounds Nitriles Azacyclic compounds Monoalkylamines Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Macrolactam - Alpha-amino acid amide - Alpha-amino acid or derivatives - Phenoxy compound - Phenol ether - Alkyl aryl ether - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Oxazole - Heteroaromatic compound - Azole - Tertiary alcohol - Secondary carboxylic acid amide - Secondary alcohol - Lactam - Carboxamide group - Amino acid or derivatives - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Carbonitrile - Nitrile - Cyanide - Organic oxygen compound - Carbonyl group - Alcohol - Organic nitrogen compound - Organic oxide - Primary amine - Organooxygen compound - Primary aliphatic amine - Amine - Hydrocarbon derivative - Organonitrogen 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