COC1CC(C)CC2=C(OC)C(=O)\C(=C/NC(C)(C)C)C(=NC(=O)C(C)=CC=CC(OC)C(OC(N)=O)C(C)=CC(C)C1O)C2=O

InChIKey=SVDZUQLPVCVSCL-VQBYCLGKSA-N

C34H49N3O9

643.778

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

O-quinomethanes M-quinomethanes Cyclohexenones Vinylogous esters Vinylogous amides Carbamate esters Secondary alcohols N-acylimines Allylamines Azacyclic compounds Enamines Dialkylamines Dialkyl ethers Propargyl-type 1,3-dipolar organic compounds Organic oxides Hydrocarbon derivatives

Aliphatic heteropolycyclic compounds

Macrolactam - M-quinomethane - O-quinomethane - Quinomethane - Cyclohexenone - Carbamic acid ester - Vinylogous ester - Vinylogous amide - Ketone - Secondary alcohol - N-acylimine - Cyclic ketone - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Enamine - Ether - Allylamine - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Amine - Carbonyl group - Alcohol - Organic nitrogen 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