C[C@@H](CO)N1C[C@H](C)[C@@H](CN(C)C(=O)Nc2cccc3ccccc23)OCCCC[C@H](C)Oc2ccc(NS(=O)(=O)c3cn(C)cn3)cc2C1=O

InChIKey=OQAIXMVZSOTSGY-CBUCOWSNSA-N

C37H48N6O7S

720.89

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Sulfanilides Naphthalenes Alkyl aryl ethers Organosulfonamides N-substituted imidazoles Tertiary carboxylic acid amides Aminosulfonyl compounds Heteroaromatic compounds Ureas Lactams Oxacyclic compounds Azacyclic compounds Dialkyl ethers Primary alcohols Carbonyl compounds Organonitrogen compounds Hydrocarbon derivatives Organic oxides

Aromatic heteropolycyclic compounds

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