Compound Identification
SMILES
OC[C@@H](CC1=CC=CC=C1)NC(=O)C[C@H]1CC=CCCCC(=O)OC[C@H](COCC2=CC=CC=C2)NC1=O
InChIKey
InChIKey=YUHBQKUSRCRZGH-PFBJBMPXSA-N
Formula
C30H38N2O6
Mass
522.642
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
Amphetamines and derivatives Benzylethers Secondary carboxylic acid amides Carboxylic acid esters Lactams Lactones Monocarboxylic acids and derivatives Dialkyl ethers Azacyclic compounds Oxacyclic compounds Carbonyl compounds Primary alcohols Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Macrolactam - Amphetamine or derivatives - Benzylether - Monocyclic benzene moiety - Benzenoid - Carboxamide group - Carboxylic acid ester - Lactam - Lactone - Secondary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic heteromonocyclic 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