Compound Identification
SMILES
COC1=CC2=C(C=C1)C1=C(C3CCCCC3)C3=C4C=C(C=C3)C(=O)NS(=O)(=O)N(C)CCCN(C)C(=O)C(CN14)=C2
InChIKey
InChIKey=KTHHACXJWUSTDW-UHFFFAOYSA-N
Formula
C31H36N4O5S
Mass
576.71
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
Benzazepines Pyrroloazepines 3-alkylindoles Anisoles Alkyl aryl ethers Azepines Substituted pyrroles Tertiary carboxylic acid amides Organic sulfuric acids and derivatives Heteroaromatic compounds Lactams Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Benzazepine - Pyrroloazepine - 3-alkylindole - Indole or derivatives - Indole - Anisole - Phenol ether - Azepine - Alkyl aryl ether - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Tertiary carboxylic acid amide - Pyrrole - Organic sulfuric acid or derivatives - Lactam - Carboxamide group - Azacycle - Carboxylic acid derivative - Ether - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - 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