Compound Identification
SMILES
CO[C@H]1C[C@H](C)CC2=C(O)C(NC(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](C\C(C)=C\[C@H](C)[C@H]1O)OC(N)=O)=CC(O)=C2NCC=C
InChIKey
InChIKey=NFLDZIUVMRBQBC-FSHHJWGSSA-N
Formula
C32H47N3O8
Mass
601.741
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 alkylarylamines 1-hydroxy-2-unsubstituted benzenoids Carbamate esters Secondary carboxylic acid amides Secondary alcohols Lactams Polyols Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Secondary aliphatic/aromatic amine - Benzenoid - Carbamic acid ester - Amino acid or derivatives - Carboxamide group - Lactam - Secondary alcohol - Secondary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Polyol - Organoheterocyclic compound - Secondary amine - Organic oxide - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Alcohol - 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