Compound Identification
SMILES
CO[C@H]1C[C@H](C)CC2=C(N)C(=O)C=C(N(CC(=O)C3=CC(Cl)=C(Cl)C=C3)C(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@H]1O)C2=O
InChIKey
InChIKey=IBJVZURONIIFTC-YAVWJVNQSA-N
Formula
C36H43Cl2N3O9
Mass
732.65
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 Aryl alkyl ketones Benzoyl derivatives Dichlorobenzenes Aryl chlorides Vinylogous amides Tertiary carboxylic acid amides Carbamate esters Secondary alcohols Lactams Cyclic ketones Azacyclic compounds Enamines Dialkyl ethers Organochlorides Hydrocarbon derivatives Organic oxides Monoalkylamines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Alkyl-phenylketone - Phenylketone - 1,2-dichlorobenzene - Aryl ketone - Aryl alkyl ketone - Benzoyl - Halobenzene - Chlorobenzene - Monocyclic benzene moiety - Aryl halide - Benzenoid - Aryl chloride - Carbamic acid ester - Tertiary carboxylic acid amide - Vinylogous amide - Cyclic ketone - Secondary alcohol - Lactam - Amino acid or derivatives - Ketone - Carboxamide group - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Enamine - Ether - Organooxygen compound - Primary amine - Organic nitrogen compound - Amine - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organochloride - Organohalogen compound - Primary aliphatic amine - 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