CN(C[C@@H](CC(=O)C[C@H]1COCCCCCCC[C@H](CC(=O)[C@@H]2[C@@H]3[C@H](CN2C1=O)C3(C)C)C(=O)C(=O)CCC=C)C(C)(C)C)S(=O)(=O)C1=CC=CS1

InChIKey=XOXIYFHGPHBXSA-SDVAFVKWSA-N

C40H60N2O8S2

761.05

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Piperidines Alpha-diketones Organosulfonamides Thiophenes Tertiary carboxylic acid amides Pyrrolidines Aminosulfonyl compounds Heteroaromatic compounds Tertiary amines Amino acids and derivatives Lactams Oxacyclic compounds Azacyclic compounds Dialkyl ethers Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Macrolactam - Alpha-diketone - Piperidine - Organosulfonic acid amide - Pyrrolidine - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary carboxylic acid amide - Thiophene - Aminosulfonyl compound - Heteroaromatic compound - Carboxamide group - Tertiary amine - Ketone - Lactam - Amino acid or derivatives - Organoheterocyclic compound - Azacycle - Ether - Oxacycle - Dialkyl ether - Carboxylic acid derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Amine - 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