Compound Identification
SMILES
CC[C@H]1C[C@@H]2[C@H]3O[C@H]3[C@H]3[C@H](C[C@H]4\C=C\C(\O)=C5\C(=O)N[C@@H](CCCNC(=O)\C=C/C[C@H]34)C5=O)C2[C@H]1C
InChIKey
InChIKey=APTVLKXCJPLIGF-PLRQYKRSSA-N
Formula
C29H38N2O5
Mass
494.632
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
Monoterpenoids Oxepanes Pyrrolidine-3-ones Pyrrolidine-2-ones Vinylogous acids Secondary carboxylic acid amides Lactams Ketones Oxacyclic compounds Azacyclic compounds Dialkyl ethers Enols Epoxides Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Macrolactam - Monoterpenoid - Oxepane - Pyrrolidone - 3-pyrrolidone - 2-pyrrolidone - Pyrrolidine - Vinylogous acid - Carboxamide group - Ketone - Lactam - Secondary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Enol - Oxirane - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Carbonyl group - 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