CC[C@H](NC[C@@H]1CC2=CC(OC[C@H](C)NC(=O)C3=CC(=CC(=C3)C(=O)N1)N(C)S(C)(=O)=O)=CC=C2)C(=O)NCC(C)C

InChIKey=NEEUNENCTTURRW-PPNCUWOSSA-N

C30H43N5O6S

601.76

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

Alpha amino acid amides Sulfanilides Alkyl aryl ethers Aralkylamines Organosulfonamides Organic sulfonamides N-acyl amines Aminosulfonyl compounds Secondary carboxylic acid amides Lactams Azacyclic compounds Oxacyclic compounds Dialkylamines Carbonyl compounds Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Macrolactam - Alpha-amino acid amide - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Sulfanilide - Alkyl aryl ether - Aralkylamine - N-acyl-amine - Fatty acyl - Fatty amide - Benzenoid - Organic sulfonic acid amide - Organosulfonic acid amide - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Sulfonyl - Organosulfonic acid or derivatives - Amino acid or derivatives - Carboxamide group - Lactam - Secondary carboxylic acid amide - Oxacycle - Azacycle - Carboxylic acid derivative - Secondary aliphatic amine - Ether - Organoheterocyclic compound - Secondary amine - Organic oxide - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Amine - Organic nitrogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen 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