Compound Identification
SMILES
CO[C@H]1C[C@H](C)CC2=C(NC3=NC=CS3)C(=O)C=C(NC(=O)\C(C)=C\C=C/[C@H](OC)[C@@H](OC(N)=O)\C(C)=C\[C@H](C)[C@H]1O)C2=O
InChIKey
InChIKey=NSGYSSJYLQINPG-HSHPMGMFSA-N
Formula
C31H40N4O8S
Mass
628.74
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
2-amino-1,3-thiazoles Vinylogous amides Heteroaromatic compounds Carbamate esters Secondary carboxylic acid amides Secondary alcohols Lactams Cyclic ketones Enamines Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - 1,3-thiazol-2-amine - Azole - Heteroaromatic compound - Vinylogous amide - Carbamic acid ester - Thiazole - Carboxamide group - Ketone - Lactam - Secondary alcohol - Cyclic ketone - Secondary carboxylic acid amide - Carboxylic acid derivative - Dialkyl ether - Enamine - Ether - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Amine - Alcohol - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen 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