Compound Identification
SMILES
ONC(=O)[C@H]1CCCCOC2=CC=C(C[C@H](NC(=O)[C@@H]1CCCC1=CC(Br)=CC(Br)=C1)C(=O)C1=CC=CC=C1)C=C2
InChIKey
InChIKey=IGKZHEJCICMYIH-ULNSLHSMSA-N
Formula
C32H34Br2N2O5
Mass
686.441
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
Alkyl-phenylketones Benzoyl derivatives Aryl alkyl ketones Bromobenzenes Alkyl aryl ethers Aryl bromides Secondary carboxylic acid amides Lactams Hydroxamic acids Oxacyclic compounds Azacyclic compounds Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Alkyl-phenylketone - Phenylketone - Aryl ketone - Aryl alkyl ketone - Benzoyl - Alkyl aryl ether - Halobenzene - Bromobenzene - Aryl halide - Aryl bromide - Benzenoid - Monocyclic benzene moiety - Secondary carboxylic acid amide - Lactam - Hydroxamic acid - Carboxamide group - Ketone - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organic oxide - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen 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