Compound Identification
SMILES
C[C@H](CO)N1C[C@@H](C)[C@H](CN(C)CC2=CC=NC=C2)OCCCC[C@H](C)OC2=C(C=C(NS(=O)(=O)C3=CC=C(C)C=C3)C=C2)C1=O
InChIKey
InChIKey=CEIZHSCRNFMPMR-UYICUSKSSA-N
Formula
C35H48N4O6S
Mass
652.85
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Macrolactams
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Macrolactams
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Macrolactams
Alternative Parents
P-toluenesulfonamides Sulfanilides Benzenesulfonamides Benzenesulfonyl compounds Alkyl aryl ethers Aralkylamines Pyridines and derivatives Organosulfonamides Tertiary carboxylic acid amides Aminosulfonyl compounds Heteroaromatic compounds Trialkylamines Amino acids and derivatives Lactams Azacyclic compounds Oxacyclic compounds Dialkyl ethers Organic oxides Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - P-toluenesulfonamide - Sulfanilide - Benzenesulfonamide - Tosyl compound - Benzenesulfonyl group - Alkyl aryl ether - Toluene - Aralkylamine - Pyridine - Organosulfonic acid amide - Monocyclic benzene moiety - Benzenoid - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Tertiary carboxylic acid amide - Sulfonyl - Heteroaromatic compound - Organosulfonic acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxamide group - Lactam - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Amine - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Primary alcohol - Aromatic heteropolycyclic compound
Description
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.
External Descriptors
Not available