Compound Identification
SMILES
COC1CC(C)CC2=C(OC)C(=O)C(=CNN(C)C)C(=NC(=O)C(C)=CC=CC(OC)C(OC(N)=O)C(C)=CC(C)C1O)C2=O
InChIKey
InChIKey=QOKGLDHCXCAVJC-UHFFFAOYSA-N
Formula
C32H46N4O9
Mass
630.739
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
O-quinomethanes M-quinomethanes Cyclohexenones Vinylogous esters Vinylogous amides Carbamate esters Secondary alcohols N-acylimines Propargyl-type 1,3-dipolar organic compounds Dialkyl ethers Azacyclic compounds Alkylhydrazines Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Macrolactam - M-quinomethane - O-quinomethane - Quinomethane - Cyclohexenone - Carbamic acid ester - Vinylogous amide - Vinylogous ester - Ketone - Secondary alcohol - N-acylimine - Cyclic ketone - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Dialkyl ether - Ether - Alkylhydrazine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrazine derivative - Organonitrogen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - 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