CC1=CC=C(C=C1)S(=O)(=O)N(CCCN)CCCN(CCCN1CCCCCCCCCCCC1=O)S(=O)(=O)C1=CC=C(C)C=C1

InChIKey=LSCGWDJOPYYCKP-UHFFFAOYSA-N

C35H56N4O5S2

676.98

Organic compounds

Phenylpropanoids and polyketides

Macrolactams

Not available

Not available

Macrolactams

N,N-disubstituted p-toluenesulfonamides Benzenesulfonamides Benzenesulfonyl compounds Organosulfonamides Tertiary carboxylic acid amides Aminosulfonyl compounds Lactams Amino acids and derivatives Azacyclic compounds Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds

Aromatic heteromonocyclic compounds

Macrolactam - N,n-disubstituted p-toluenesulfonamide - P-toluenesulfonamide - Benzenesulfonamide - Tosyl compound - Benzenesulfonyl group - Toluene - Monocyclic benzene moiety - Organosulfonic acid amide - Benzenoid - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Tertiary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Lactam - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organic oxide - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organopnictogen compound - Amine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic 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