Compound Identification
SMILES
C[C@H]1[C@@H](OC(=O)[C@H]2[C@@H]3O[C@@]4(C=C3)[C@@H]2C(=O)N(CCCO)[C@@H]4C(=O)N(CC2=CC=CC=C2)C\C=C/CCC(=O)N1C)C1=CC=CC=C1
InChIKey
InChIKey=CFMWBEYZKBGXCV-JNWQDMNYSA-N
Formula
C36H41N3O7
Mass
627.738
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
Macrolides and analogues Alpha amino acids and derivatives Isoindolones Furopyrroles Pyrrolidine-2-ones Benzene and substituted derivatives N-alkylpyrrolidines Tertiary carboxylic acid amides Pyrroles Oxolanes Dihydrofurans Furans Carboxylic acid esters Lactones Lactams Alkanolamines Azacyclic compounds Oxacyclic compounds Dialkyl ethers Monocarboxylic acids and derivatives Organic oxides Primary alcohols Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Macrolide - Alpha-amino acid or derivatives - Isoindolone - Isoindoline - Isoindole or derivatives - Furopyrrole - Monocyclic benzene moiety - Benzenoid - N-alkylpyrrolidine - 2-pyrrolidone - Pyrrolidone - Dihydrofuran - Furan - Tertiary carboxylic acid amide - Oxolane - Pyrrole - Pyrrolidine - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Dialkyl ether - Ether - Alkanolamine - Oxacycle - Azacycle - Organoheterocyclic compound - Primary alcohol - Organic nitrogen compound - Alcohol - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Carbonyl group - Organic oxygen 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