CO[C@H]1C[C@H](C)CC2=C3N=C(NC(NCC4=CC=CC=C4)=NC)NC3=CC(=NC(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@H]1O)C2=O

InChIKey=MGQYGBCKFZNKNV-WRJALTGASA-N

C38H49N7O7

715.852

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Benzene and substituted derivatives Imidazoles Heteroaromatic compounds Carbamate esters Secondary alcohols N-acylimines Ketones Guanidines Propargyl-type 1,3-dipolar organic compounds Dialkyl ethers Carboximidamides Azacyclic compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Macrolactam - Monocyclic benzene moiety - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Carbamic acid ester - Guanidine - Ketone - Secondary alcohol - N-acylimine - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Hydrocarbon derivative - Organic oxide - Imine - Organic oxygen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Alcohol - Organic nitrogen 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