CN1[C@@H](CCCN=C(N)N)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(N)=O)C(C)(C)SSC(C)(C)[C@H](NC(C)=O)C1=O

InChIKey=FTNKTQMIRUQUMO-LBTBCDHLSA-N

C25H43N9O8S2

661.79

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

N-acyl-alpha amino acids and derivatives Tertiary carboxylic acid amides Acetamides Secondary carboxylic acid amides Primary carboxylic acid amides Guanidines Organic disulfides Lactams Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carboximidamides Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteromonocyclic compounds

Macrolactam - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Acetamide - Tertiary carboxylic acid amide - Carboxamide group - Guanidine - Lactam - Organic disulfide - Primary carboxylic acid amide - Secondary carboxylic acid amide - Carboxylic acid derivative - Carboxylic acid - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Aliphatic heteromonocyclic 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