Compound Identification
SMILES
CN1[C@@H](CO)C(=O)N[C@H](CC2=CC=C(Cl)C=C2)C(=O)NC\C=C\C2=CC=CC=C2OCCN[C@@H](C2CCCCC2)C1=O
InChIKey
InChIKey=ISEMOGOWTCFUGI-JOQTZGRISA-N
Formula
C32H41ClN4O5
Mass
597.15
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
Alpha amino acids and derivatives Chlorobenzenes Alkyl aryl ethers Aryl chlorides Tertiary carboxylic acid amides Secondary carboxylic acid amides Lactams Oxacyclic compounds Dialkylamines Azacyclic compounds Primary alcohols Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Alpha-amino acid or derivatives - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Tertiary carboxylic acid amide - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Lactam - Secondary amine - Azacycle - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Ether - Secondary aliphatic amine - Primary alcohol - Organic oxide - Hydrocarbon derivative - Organohalogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Alcohol - Organochloride - Organonitrogen compound - Amine - Organooxygen 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