Compound Identification
SMILES
CO[C@H]1C[C@H](C)CC2=C(NCC=C)C(=O)C=C(NC(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=C)\C(C)=C\[C@H](C)[C@H]1O)C2=O
InChIKey
InChIKey=YTLUWBHOKBLONJ-MFWPWKKDSA-N
Formula
C32H45N3O7
Mass
583.726
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
Vinylogous amides Secondary carboxylic acid amides Secondary alcohols Lactams Ketene acetals Cyclic ketones Amino acids and derivatives Enamines Dialkylamines Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Macrolactam - Vinylogous amide - Amino acid or derivatives - Carboxamide group - Ketene acetal or derivatives - Ketone - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Cyclic ketone - Azacycle - Organoheterocyclic compound - Dialkyl ether - Carboxylic acid derivative - Secondary amine - Secondary aliphatic amine - Enamine - Ether - Organic oxide - Amine - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Alcohol - Organooxygen compound - 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