Compound Identification
SMILES
COC1=C2NC(=O)\C=C\C=C/C=C/C(C)C(O)CC(=O)\C(C)=C\CC(O)\C=C\C(C)C(O)C(C)\C=C(C)/C(=O)C3=C(C1=O)C(=CC(C)=C3O)C2=O
InChIKey
InChIKey=LTHCNGAEDWPRCS-HODGDDQQSA-N
Formula
C40H47NO10
Mass
701.813
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
Naphthoquinones Quinones Aryl ketones Phenols Vinylogous esters Vinylogous amides Vinylogous acids Secondary carboxylic acid amides Secondary alcohols Lactams Polyols Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Naphthoquinone - Naphthalene - Quinone - Aryl ketone - Phenol - Benzenoid - Vinylogous amide - Vinylogous acid - Vinylogous ester - Carboxamide group - Ketone - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Cyclic ketone - Organoheterocyclic compound - Polyol - Carboxylic acid derivative - Azacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Alcohol - Hydrocarbon derivative - 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