CO[C@H]1C[C@H](C)CC2=C(NCC=C)C(=O)C=C(NC(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@H]1OC(=O)CN)C2=O

InChIKey=ZFBCWWKALCIUTI-OCJCMWQISA-N

C33H46N4O9

642.75

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Alpha amino acid esters Vinylogous amides Carbamate esters Secondary carboxylic acid amides Lactams Cyclic ketones Carboxylic acid esters Monocarboxylic acids and derivatives Enamines Dialkylamines Dialkyl ethers Azacyclic compounds Organic oxides Monoalkylamines Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Alpha-amino acid ester - Macrolactam - Alpha-amino acid or derivatives - Carbamic acid ester - Vinylogous amide - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Ketone - Lactam - Secondary carboxylic acid amide - Cyclic ketone - Organoheterocyclic compound - Azacycle - Secondary amine - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Enamine - Ether - Monocarboxylic acid or derivatives - Organic nitrogen compound - Carbonyl group - Primary amine - Hydrocarbon derivative - Amine - Organic oxide - Primary aliphatic amine - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aliphatic 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