Compound Identification
SMILES
COC1CC(C)CC2=C(OC)C(=O)\C(=C\NN3CCOCC3)C(=NC(=O)\C(C)=C\C=C/C(OC)C(OC(N)=O)\C(C)=C\C(C)C1O)C2=O
InChIKey
InChIKey=ZSALWPGZXAZTAX-LLDLSZAYSA-N
Formula
C34H48N4O10
Mass
672.776
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
M-quinomethanes O-quinomethanes Cyclohexenones Morpholines Vinylogous esters Vinylogous amides Carbamate esters Secondary alcohols N-acylimines Alkylhydrazines Azacyclic compounds Dialkyl ethers Oxacyclic compounds Propargyl-type 1,3-dipolar organic compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Macrolactam - M-quinomethane - O-quinomethane - Quinomethane - Cyclohexenone - Morpholine - Oxazinane - Carbamic acid ester - Vinylogous amide - Vinylogous ester - Ketone - Secondary alcohol - N-acylimine - Cyclic ketone - Organoheterocyclic compound - Azacycle - Organic 1,3-dipolar compound - Oxacycle - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Dialkyl ether - Ether - Alkylhydrazine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrazine derivative - Organic oxide - Organonitrogen compound - 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