Compound Identification
SMILES
CC(C)(C)OC(O)=NC1CCCCCCCCCC(N=C(O)C2C3C(CN2C1=O)C3(C)C)C(=O)C(=O)NCC=C
InChIKey
InChIKey=KCGQQQFOEAVEDN-UHFFFAOYSA-N
Formula
C30H48N4O6
Mass
560.736
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Macrolactams
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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
Alpha amino acids and derivatives Piperidines Tertiary carboxylic acid amides Pyrrolidines Cyclic carboximidic acids Secondary carboxylic acid amides Lactams Ketones Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Macrolactam - Alpha-amino acid or derivatives - Piperidine - Pyrrolidine - Tertiary carboxylic acid amide - Cyclic carboximidic acid - Carboxamide group - Ketone - Lactam - Secondary carboxylic acid amide - Carboximidic acid derivative - Carboxylic acid derivative - Azacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - 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