COC1=CC=C(CN(C)C[C@H]2OCCCC[C@H](C)OC3=C(C=C(NC(=O)NC4=CC=CC=C4)C=C3)C(=O)N(C[C@H]2C)[C@H](C)CO)C=C1

InChIKey=UCPZOXKPGUJWAP-RIKJNLPISA-N

C37H50N4O6

646.829

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

N-phenylureas Anisoles Benzylamines Methoxybenzenes Phenoxy compounds Phenylmethylamines Alkyl aryl ethers Aralkylamines Tertiary carboxylic acid amides Ureas Lactams Amino acids and derivatives Trialkylamines Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary alcohols

Aromatic heteropolycyclic compounds

Macrolactam - N-phenylurea - Anisole - Phenoxy compound - Benzylamine - Phenol ether - Phenylmethylamine - Methoxybenzene - Alkyl aryl ether - Aralkylamine - Benzenoid - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Amino acid or derivatives - Urea - Carboxamide group - Lactam - Tertiary amine - Tertiary aliphatic amine - Azacycle - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Amine - Carbonyl group - Organic oxygen compound - Primary alcohol - Organic nitrogen compound - Organooxygen compound - Alcohol - Organic oxide - 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