Compound Identification
SMILES
COC1C=CC=C(C)CC2=CC(NC(=O)CC(O)C(C)=CC(C)C(O)CC1=O)=C(Cl)C(O)C2
InChIKey
InChIKey=AANSHDKGOCAZCQ-UHFFFAOYSA-N
Formula
C25H34ClNO6
Mass
480.0
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
Secondary carboxylic acid amides Secondary alcohols Lactams Cyclic ketones Chlorohydrins Vinyl chlorides Polyols Dialkyl ethers Chloroalkenes Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Macrolactam - Carboxamide group - Chlorohydrin - Halohydrin - Ketone - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Cyclic ketone - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Polyol - Chloroalkene - Haloalkene - Vinyl chloride - Vinyl halide - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Alcohol - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Organic oxide - Aliphatic 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