Compound Identification
SMILES
COC1=C2C=C(OC3=CC=C(C=C3)\C=C/C(=O)[C@@H]3CC(=O)NCCCN2CCCCN(CCCN3)C(C)=O)C=C1
InChIKey
InChIKey=YSFRRJNMGSCWSG-ZXRXZOBYSA-N
Formula
C31H40N4O5
Mass
548.684
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
Diarylethers Beta amino acids and derivatives Dialkylarylamines Anisoles Alkyl aryl ethers Tertiary carboxylic acid amides Acetamides Secondary carboxylic acid amides Lactams Ketones Oxacyclic compounds Dialkylamines Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Beta amino acid or derivatives - Diaryl ether - Anisole - Phenol ether - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Alkyl aryl ether - Benzenoid - Acetamide - Tertiary carboxylic acid amide - Tertiary amine - Ketone - Secondary carboxylic acid amide - Lactam - Carboxamide group - Amino acid or derivatives - Oxacycle - Carboxylic acid derivative - Secondary aliphatic amine - Azacycle - Ether - Organoheterocyclic compound - Secondary amine - Amine - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - 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