COC1=NC(=CC(O[C@@H]2C[C@@H]3[C@@H](C2)C(=O)N(C)CCCC\C=C/[C@H]2C[C@]2(NC3=O)C(O)=O)=N1)C1=CC=CC=C1

InChIKey=SSDGPAAYKSSYSI-KBRSMJGZSA-N

C29H34N4O6

534.613

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Phenylpyrimidines Alpha amino acids and derivatives Alkyl aryl ethers Benzene and substituted derivatives Cyclopropanecarboxylic acids Tertiary carboxylic acid amides Heteroaromatic compounds Tertiary amines Secondary carboxylic acid amides Amino acids Lactams Carboxylic acids Azacyclic compounds Monocarboxylic acids and derivatives Hydrocarbon derivatives Organic oxides Carbonyl compounds

Aromatic heteropolycyclic compounds

Macrolactam - 4-phenylpyrimidine - Alpha-amino acid or derivatives - Alkyl aryl ether - Cyclopropanecarboxylic acid or derivatives - Pyrimidine - Benzenoid - Cyclopropanecarboxylic acid - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Heteroaromatic compound - Tertiary amine - Secondary carboxylic acid amide - Amino acid or derivatives - Amino acid - Carboxamide group - Lactam - Azacycle - Carboxylic acid derivative - Carboxylic acid - Organoheterocyclic compound - Ether - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Amine - Organic oxide - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - 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