Compound Identification
SMILES
C[C@@H]1NC(=O)OC[C@H]2O[C@@H](CNC(=O)[C@H](CCC(N)=O)NC(=O)OC[C@H]3O[C@@H](CNC1=O)[C@H](OC1=CC=C(C)C=C1)[C@@H](OC1=CC=C(C)C=C1)[C@@H]3OC1=CC=C(C)C=C1)[C@H](OC1=CC=C(C)C=C1)[C@@H](OC1=CC=C(C)C=C1)[C@H]2OC1=CC=C(C)C=C1
InChIKey
InChIKey=CUYWDCDAUGZFTB-IELYSHEESA-N
Formula
C66H75N5O15
Mass
1178.346
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 Phenoxy compounds Phenol ethers Toluenes Alkyl aryl ethers Oxanes Fatty amides Monosaccharides Carbamate esters Secondary carboxylic acid amides Primary carboxylic acid amides Lactams Oxacyclic compounds Azacyclic compounds Dialkyl ethers Carbonyl compounds Organonitrogen compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Alpha-amino acid or derivatives - Phenoxy compound - Phenol ether - Alkyl aryl ether - Toluene - Oxane - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Fatty acyl - Fatty amide - Carbamic acid ester - Primary carboxylic acid amide - Secondary carboxylic acid amide - Carboxamide group - Lactam - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - 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