C[C@@H](CO)N1C[C@H](C)[C@@H](CN(C)C(=O)C2CCCCC2)OCCCC[C@H](C)OC2=C(C=C(NS(=O)(=O)C3=C(C)ON=C3C)C=C2)C1=O

InChIKey=VCHXZHCJCJLLTK-ILSPQUDCSA-N

C34H52N4O8S

676.87

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Sulfanilides Alkyl aryl ethers Organosulfonamides Tertiary carboxylic acid amides Aminosulfonyl compounds Isoxazoles Heteroaromatic compounds Tertiary amines Amino acids and derivatives Lactams Oxacyclic compounds Azacyclic compounds Dialkyl ethers Primary alcohols Carbonyl compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

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