Compound Identification
SMILES
CC=C(NC(=O)C1=CSC(=N1)C1=CSC(=N1)C1=NC2=C(C=C1)C1=NC(=CS1)C(=O)NC(C(C)O)C(=O)NC(=CC)C1=NC(=CS1)C(=O)NC(C1=NC(=CS1)C(=O)NC(C(C)O)C1=NC2=CS1)C(C)(C)O)C(=O)NCC(C)O
InChIKey
InChIKey=FEORQDDAQBRWPT-UHFFFAOYSA-N
Formula
C48H49N13O10S6
Mass
1160.36
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
N-acyl-alpha amino acids and derivatives Alpha amino acid amides Thiazolecarboxamides 2-heteroaryl carboxamides 2,4-disubstituted thiazoles N-acyl amines Pyridines and derivatives Tertiary alcohols Heteroaromatic compounds Secondary carboxylic acid amides Lactams Secondary alcohols Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organic oxides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Macrolactam - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - 2-heteroaryl carboxamide - Thiazolecarboxylic acid or derivatives - Thiazolecarboxamide - 2,4-disubstituted 1,3-thiazole - N-acyl-amine - Pyridine - Azole - Heteroaromatic compound - Thiazole - Tertiary alcohol - Carboxamide group - Lactam - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Alcohol - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - 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