C[C@H](CO)N1C[C@@H](C)[C@@H](CN(C)C(=O)C2=CC=NC=C2)OCCCC[C@H](C)OC2=C(C=C(NS(=O)(=O)C3=CN(C)C=N3)C=C2)C1=O

InChIKey=ODNWKNHKBXENDA-IDCDSMMUSA-N

C32H44N6O7S

656.8

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Sulfanilides Pyridinecarboxamides Alkyl aryl ethers Organosulfonamides N-substituted imidazoles Tertiary carboxylic acid amides Aminosulfonyl compounds Heteroaromatic compounds Tertiary amines Amino acids and derivatives Lactams Oxacyclic compounds Azacyclic compounds Dialkyl ethers Primary alcohols Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Macrolactam - Sulfanilide - Pyridinecarboxamide - Pyridine carboxylic acid or derivatives - Alkyl aryl ether - N-substituted imidazole - Pyridine - Organosulfonic acid amide - Benzenoid - Azole - Imidazole - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary carboxylic acid amide - Aminosulfonyl compound - Carboxamide group - Tertiary amine - Amino acid or derivatives - Lactam - Oxacycle - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Dialkyl ether - Ether - Amine - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Alcohol - Primary alcohol - 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