Compound Identification
SMILES
CO[C@H]1C[C@H](C)CC2=C(NC(=O)NCC3=CC=CC=C3)C(=O)C=C(NC(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@H]1O)C2=O
InChIKey
InChIKey=IARYXFMLMZAECQ-WQOHEETESA-N
Formula
C36H46N4O9
Mass
678.783
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
Benzene and substituted derivatives Vinylogous amides Carbamate esters Ureas Secondary carboxylic acid amides Secondary alcohols Lactams Cyclic ketones Dialkyl ethers Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Monocyclic benzene moiety - Benzenoid - Carbamic acid ester - Vinylogous amide - Carboxamide group - Ketone - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Urea - Cyclic ketone - Ether - Carboxylic acid derivative - Dialkyl ether - Azacycle - Organoheterocyclic compound - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Organic oxide - Hydrocarbon derivative - 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