COC1CC(C)CC2=C(OC)C(=O)\C(=C/NN3CCCCC3)C(=NC(=O)\C(C)=C/C=C\C(OC)C(OC(N)=O)\C(C)=C/C(C)C1O)C2=O

InChIKey=SOWFYJFDGWWPGL-YCFLNDBLSA-N

C35H50N4O9

670.804

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

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

Aliphatic heteropolycyclic compounds

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