Compound Identification
SMILES
COC[C@@H]1CCCN1S(=O)(=O)NC(=O)[C@@]12C[C@H]1C=CCCCCC[C@H](OC(=O)NC(C)(C)C)C(=O)N1CCC[C@H]1C(=O)N2
InChIKey
InChIKey=OWOYMBSOCUHDEU-DDABLGSASA-N
Formula
C29H47N5O8S
Mass
625.78
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
Alpha amino acid amides Cyclopropanecarboxylic acids and derivatives Tertiary carboxylic acid amides Pyrrolidines Organic sulfuric acids and derivatives Carbamate esters Secondary carboxylic acid amides Lactams Dialkyl ethers Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Macrolactam - Alpha-amino acid amide - Alpha-amino acid or derivatives - Cyclopropanecarboxylic acid or derivatives - Carbamic acid ester - Tertiary carboxylic acid amide - Pyrrolidine - Organic sulfuric acid or derivatives - Carboxamide group - Lactam - Secondary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organonitrogen 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