Compound Identification
SMILES
C[C@H]1OCC[C@@]2(C)O[C@H]2C[C@H](NC(=O)C[C@H](O)C2(CCC2)C(=O)[C@H](CC=C)[C@@H]1O)C1=CC2=C(SC(C)=N2)C=C1
InChIKey
InChIKey=KCDOVMCQUKGKDS-IYKXAJQFSA-N
Formula
C30H40N2O6S
Mass
556.72
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
Azaspirodecane derivatives Benzothiazoles Benzenoids Thiazoles Heteroaromatic compounds Secondary carboxylic acid amides Secondary alcohols Lactams Ketones Azacyclic compounds Oxacyclic compounds Dialkyl ethers Epoxides Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Azaspirodecane - 1,3-benzothiazole - Benzenoid - Azole - Heteroaromatic compound - Thiazole - Carboxamide group - Ketone - Lactam - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid derivative - Dialkyl ether - Oxirane - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - 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