CC(C)CN([C@H](CO)CCCCNC(=S)[C@H](CC1C=NC2=CC=CC=C12)NS(=O)(=O)C1=CC=C(C)C=C1)S(=O)(=O)C1=CC=C(C)C=C1

InChIKey=RISOUSJEDQAWAS-XBVKBMTLSA-N

C35H46N4O5S3

698.96

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Benzenesulfonamides 3-alkylindoles Benzenesulfonyl compounds Organosulfonamides Thioamides Aminosulfonyl compounds Thiocarboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Thiocarbonyl compounds Primary alcohols Organic oxides Imines Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - 3-alkylindole - Indole - Indole or derivatives - Benzenesulfonyl group - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Thioamide - Aminosulfonyl compound - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Thiocarboxylic acid amide - Alcohol - Hydrocarbon derivative - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic nitrogen compound - Imine - Thiocarbonyl group - Organic oxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as n,n-disubstituted p-toluenesulfonamides. These are p-toluenesulfonamide derivatives in which the sulfonamide moiety is N,N-disubstituted.

Not available