Compound Identification
SMILES
COC(=O)CC1=CSC(NC(=O)[C@@H]2CCCCNC(=O)OCCC[C@@H]([C@@H](CC(C)C)C(=O)N2)C(=O)OC(C)(C)C)=N1
InChIKey
InChIKey=BGKAMXHTJGJLAT-HBMCJLEFSA-N
Formula
C28H44N4O8S
Mass
596.74
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 N-arylamides 2,4-disubstituted thiazoles Dicarboxylic acids and derivatives Methyl esters Heteroaromatic compounds Carbamate esters Secondary carboxylic acid amides Lactams Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Macrolactam - Alpha-amino acid amide - Alpha-amino acid or derivatives - N-arylamide - 2,4-disubstituted 1,3-thiazole - Dicarboxylic acid or derivatives - Azole - Heteroaromatic compound - Methyl ester - Carbamic acid ester - Thiazole - Carboxamide group - Carboxylic acid ester - Secondary carboxylic acid amide - Lactam - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic 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