CO[C@H](C)C1[C@H](C)C[C@@H]2[C@H]3CC4\C=C\C(\O)=C5\C(=O)N[C@@H](C(O)CCNC(=O)\C=C/CC4[C@H]3[C@@H]3O[C@@H]3[C@@H]12)C5=O

InChIKey=OVLYZZGOLFUBSV-KJOCMSKESA-N

C30H40N2O7

540.657

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Iridoids and derivatives Oxepanes Pyrrolidine-3-ones Pyrrolidine-2-ones Vinylogous acids Secondary carboxylic acid amides Secondary alcohols Lactams Ketones Oxacyclic compounds Azacyclic compounds Dialkyl ethers Enols Epoxides Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds

Aliphatic heteropolycyclic compounds

Macrolactam - 11-noriridane monoterpenoid - Monoterpenoid - Oxepane - 3-pyrrolidone - 2-pyrrolidone - Pyrrolidone - Pyrrolidine - Vinylogous acid - Carboxamide group - Ketone - Lactam - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Dialkyl ether - Enol - Oxirane - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Alcohol - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - 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