Compound Identification
SMILES
CC(C)[C@H](NC(=O)OC(C)(C)C)C1=NC2=C(CC3=CC=CC(=C3)C3=C4C(CCNC2=O)=CNC4=CC=C3)O1
InChIKey
InChIKey=PJYMGQAEAUHDHL-VWLOTQADSA-N
Formula
C30H34N4O4
Mass
514.626
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
3-alkylindoles 2-heteroaryl carboxamides Benzenoids Pyrroles Oxazoles Carbamate esters Heteroaromatic compounds Secondary carboxylic acid amides Lactams Azacyclic compounds Oxacyclic compounds Organic oxides Carbonyl compounds Organonitrogen compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - 3-alkylindole - Indole - Indole or derivatives - 2-heteroaryl carboxamide - Benzenoid - Azole - Oxazole - Heteroaromatic compound - Pyrrole - Carbamic acid ester - Carboxamide group - Lactam - Secondary carboxylic acid amide - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Carbonyl group - 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