CC(C)(C)NC(=O)[C@@H]1CC2CCCCC2CN1C[C@@H](O)[C@@H]1CC2=CC=C(OCCOC3=CC4=CC=CC=C4C=C3C(=O)N[C@@H](CC(N)=O)C(=O)N1)C=C2

InChIKey=BXXKSGNCOZTWCZ-BKGDRJHFSA-N

C41H53N5O7

727.903

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Alpha amino acid amides Naphthalenes Piperidinecarboxamides Alkyl aryl ethers Aralkylamines 1,2-aminoalcohols Trialkylamines Secondary carboxylic acid amides Secondary alcohols Lactams Primary carboxylic acid amides Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides

Aromatic heteropolycyclic compounds

Macrolactam - Alpha-amino acid amide - Alpha-amino acid or derivatives - Naphthalene - 2-piperidinecarboxamide - Piperidinecarboxamide - Alkyl aryl ether - Aralkylamine - Piperidine - Benzenoid - Tertiary aliphatic amine - Amino acid or derivatives - Carboxamide group - Lactam - 1,2-aminoalcohol - Primary carboxylic acid amide - Secondary alcohol - Secondary carboxylic acid amide - Tertiary amine - Oxacycle - Ether - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - Amine - Alcohol - Carbonyl group - 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