CO[C@H]1C[C@H](C)CC2=C3N=C(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)N1CCN(C)CC1

InChIKey=BXPKNONUVCYJLU-PVLDASJESA-N

C34H48N6O7

652.793

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

N-arylpiperazines Dialkylarylamines N-methylpiperazines Aminoimidazoles Heteroaromatic compounds Carbamate esters Trialkylamines Secondary alcohols N-acylimines Ketones Propargyl-type 1,3-dipolar organic compounds Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Macrolactam - N-arylpiperazine - Dialkylarylamine - N-methylpiperazine - N-alkylpiperazine - Aminoimidazole - 1,4-diazinane - Piperazine - Carbamic acid ester - Azole - Heteroaromatic compound - Imidazole - Amino acid or derivatives - N-acylimine - Tertiary amine - Tertiary aliphatic amine - Secondary alcohol - Ketone - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Amine - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - 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