Compound Identification
SMILES
CCOC(=O)O[C@@H]1\C=C(C)\CC[C@]2(CC(=O)N[C@H](C)C3=NC(=CS3)\C=C/C=C/C1=O)S(=O)SC(=O)[C@]2(C)O
InChIKey
InChIKey=BBMYPVWAZSUMJA-KOQUYDNPSA-N
Formula
C25H30N2O8S3
Mass
582.7
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
Carbonic acid diesters Thiosulfinic acid esters Thiazoles Tertiary alcohols Heteroaromatic compounds 1,2-dithiolanes Secondary carboxylic acid amides Lactams Cyclic ketones Thiocarboxylic acids and derivatives Sulfinyl compounds Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - Carbonic acid diester - Azole - Dithiolane - Heteroaromatic compound - Tertiary alcohol - Thiazole - Thiosulfinic acid ester - 1,2-dithiolane - Carboxamide group - Ketone - Lactam - Carbonic acid derivative - Secondary carboxylic acid amide - Cyclic ketone - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Thiocarboxylic acid or derivatives - Sulfinyl compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Carbonyl group - Alcohol - 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